Atypical hemolytic uremic syndrome (aHUS), C3 glomerulopathy (C3G), and paroxysmal nocturnal hemoglobinuria (PNH) are prototypical disorders of complement dysregulation. Although complement overactivation is common to all, cell surface alternative pathway dysregulation (aHUS), fluid phase alternative pathway dysregulation (C3G), or terminal pathway dysregulation (PNH) predominates resulting in the very different phenotypes seen in these diseases. The mechanism underlying the dysregulation also varies with predominant acquired autoimmune (C3G), somatic mutations (PNH), or inherited germline mutations (aHUS) predisposing to disease. Eculizumab has revolutionized the treatment of PNH and aHUS although has been less successful in C3G. With the next generation of complement therapeutic in late stage development, these archetypal complement diseases will provide the initial targets.
Atypical hemolytic uremic syndrome (aHUS), C3 glomerulopathy (C3G), and paroxysmal nocturnal hemoglobinuria (PNH) serve as exemplars of the mechanisms by which complement dysregulation may cause disease. In this review, we shall compare and contrast the underlying pathophysiological mechanisms and the response to treatments.
Classification of atypical hemolytic uremic syndrome
The last 20 years has seen striking advances in our understanding of the molecular mechanisms underlying thrombotic microangiopathies (TMAs) and with this has come a complex and rapidly evolving nomenclature . Historically, TMAs were categorized on clinical findings: HUS for renal dominant disease, thrombotic thrombocytopenic purpura (TTP) for predominant neurological involvement. Subsequently, TTP was defined by severe ADAMTS13 deficiency; HUS caused by shiga toxin-producing Escherichia coli (STEC) defined as STEC-HUS, with aHUS broadly used for all other causes of TMA. With the discovery of genetic and acquired complement dysregulation in a proportion of patients with aHUS, the term complement-mediated aHUS was used to refer to this subgroup. When reviewing historical literature, “aHUS” may refer specifically to complement-mediated TMA, or be more loosely applied to any TMA that is not TTP or STEC-HUS (reviewed ). In this review, we use the term complement-mediated aHUS when the etiology is defined as such, and use aHUS where etiology is ill defined. Current classifications describe acquired primary TMAs, inherited primary TMAs, secondary TMAs, and infection-associated TMAs (Table 1) although it should be borne in mind that underlying complement genetic predispositions often require a secondary trigger for TMA to manifest. The role of complement in secondary TMAs and infection associated TMA is yet to be defined (Fig. 1).
The pathological findings seen in complement-mediated aHUS reflect tissue responses to endothelial injury: endothelial swelling and mesangiolysis in active lesions, double contours of the basement membrane in chronic lesions (reviewed ). The absence of overt platelet fibrin thrombosis from renal biopsies of TMA has recently led to a suggested reclassification to microangiopathy +/− thrombosis .
Inherited primary complement-mediated aHUS
First described in 1998 by Warwicker et al. , mutations in factor H (CFH) are the commonest cause of inherited complement-mediated aHUS, accounting for around 25% of cases . Factor H (FH) is the most important fluid-phase regulator of the alternative pathway (AP) of complement. FH is composed of 20 complement control protein modules (CCPs), also known as short consensus repeats (SCRs). The four N-terminal CCPs (CCPs 1–4) mediate the complement regulatory functions of the protein by competing with factor B for C3b binding, accelerating the decay of the C3 convertase into its components, and acting as a cofactor for factor I-mediated proteolytic inactivation of C3b [5, 6]. The vast majority of CFH mutations seen in complement-mediated aHUS do not occur in this region, but instead in the C terminal domains (CCP 19–20) . It is this region which mediates FH self-surface binding via its interaction with C3b, sialic acid, and glycosaminoglycans [7, 8]. In complement-mediated aHUS, the mutations are usually heterozygous, do not result in a quantitative deficiency of FH but instead have variable consequences on binding to GAGs, sialic acid, and C3b which impairs cell surface complement regulation [9, 10] (reviewed4).
In addition to point mutations, its location in the RCA cluster makes CFH particularly prone to genomic rearrangements. This is an area of the genome that arose from several large genomic duplications, and these low copy repeats can cause genome instability in this region. The CFH mutations S1191L, V1197A, and combined S1191L/V1197A arose through gene conversion between CFHR1 and CFH . A hybrid (fusion) gene comprising the 21 N-terminal exons of CFH and the 2 C terminal exons of CFHR1 was demonstrated to have arisen through nonallelic homologous recombination and resulted in complement-mediated aHUS . More recently, several other hybrid genes consisting of the N-terminal exons of CFH and the 5 C-terminal exons of CFHR3 have been reported [13, 14]. As with C-terminal point mutations in CFH, these hybrid genes also result in loss of cell surface complement regulation.
Membrane cofactor protein
Membrane cofactor protein (MCP; CD46) is a surface-bound complement regulatory protein that acts as a cofactor for the factor I (FI) mediated cleavage of C3b and C4b that are deposited on host cells . Mutations in CD46 are the second commonest cause of complement-mediated aHUS accounting for around 15% of patients.
The majority of mutations are found in the extracellular domains of CD46 that are responsible for C3b and C4b binding. Unlike CFH, most CD46 mutations result in a quantitative defect in CD46 (~ 75%) .
Complement factor I
Complement factor I is a serum serine protease, which functions as a critical mediator of complement regulation by cleaving C3b and C4b in the presence of its cofactors (FH for C3b; C4BP (C4b binding protein) for C4b, CD46 and CR1 (complement receptor 1) for both .
Around 10% of complement-mediated aHUS is predisposed to by mutations in the FI gene (CFI) . The CFI mutations described in complement-mediated aHUS are all heterozygous.
C3 is the central component of the complement cascade. C3 is cleaved to form the anaphylatoxin C3a and C3b, which is highly reactive and can bind to cell surfaces via its reactive thioester. C3b can then interact with factor B (FB) in the presence of factor D to form the alternative pathway convertase introducing a positive-feedback loop.
Mutations in C3 account for around 2–10% of complement-mediated aHUS. The mutations in C3 linked to complement-mediated aHUS result in complement over activation by either (1) preventing complement regulators binding to C3 and inactivating it or by binding to FB with greater affinity [17,18,19]. These mutations result in increased complement activation on platelets and glomerular endothelium.
Complement factor B
Factor B carries the catalytic site of the complement AP convertase (C3bBb). Mutations in CFB are very rare in complement-mediated aHUS. As with C3 mutations, complement over activation occurs by impaired complement regulation or increased convertase formation . These mutations have been demonstrated to increase complement deposition on endothelial cells.
Thrombomodulin (THBD) plays a key role in regulating clot formation by the activation of protein C by thrombin and enhancing thrombin-mediated activation of plasma procarboxypeptidase B (CPB2), an inhibitor of fibrinolysis. Procarboxypeptidase B also inactivates complement-derived anaphylatoxins C3a and C5a. THBD has also been suggested to have a role in the regulation of the AP by accelerating FI-mediated inactivation of C3b .
Rare genetic variants have been described in some aHUS cohorts but their causality remains to be established .
Common genetic susceptibility factors
In addition to rare mutations, a number of common single nucleotide polymorphisms (SNPs) in CD46 and CFH have been associated with complement-mediated aHUS. A CD46 haplotype (CD46ggaac) block has been associated with a two- to threefold increased risk of complement-mediated aHUS [22,23,24]. This encompasses 2 SNPs in the promoter region of CD46, and reporter gene assays have suggested that this haplotype reduces transcriptional activity by 25% albeit without decreased CD46 cell surface expression in vivo [24, 25]. A CFH haplotype (CFH-H3; tgtgt) has been shown to increase the risk of complement-mediated aHUS two- to fourfold [22, 26]. This risk haplotype contains a SNP CFH-Val62 which has a subtle decrease in cofactor activity compared to the protective variant [27, 28].
Acquired primary complement-mediated aHUS
Acquired defects in complement regulation have been seen in the form of autoantibodies to FH. First reported in 2005, these account for ~ 10% of complement-mediated aHUS . It predominantly presents in childhood, frequently with a gastrointestinal prodrome .
There is a strong association with a homozygous deletion of CFHR3 and CFHR1, which encodes complement factor H-related proteins (FHR) 3 and 1 . Subsequently, FHR1 deficiency resulting from point mutations in CFHR1 or from a deletion incorporating CFHR1 and CFHR4 has been reported in individuals with FH autoantibody-mediated aHUS . Although this suggests a key role in the deficiency of FHR1 in the generation of FH autoantibodies, the mechanism remains obscure and several patients have been reported with factor H autoantibodies in the absence of the CFHR1/CFHR3 deletion.
The majority of autoantibodies bind to the C-terminal domain of FH, thus mimicking the defects see in the inherited form. The antibodies have been shown to reduce binding to C3b and other C3 fragments [33, 34]. They perturb FH-mediated cell surface protection and in some individuals the autoantibodies also impair cofactor activity or decay accelerating activity [33, 34].
Autoantibodies against FI have also been reported, but are rare and their functional relevance remains to be established .
Clinical presentation and outcome
The incidence of aHUS is ~ 0.4/million population . Hemolysis and ischemic organ injury, predominantly in the kidney, define the clinical presentation of aHUS . Extra-renal manifestations (cardiac, ocular, pancreatic) are reported although it is not known whether they are a direct consequence of the TMA, a direct effect of complement activation, or relate to the associated severe hypertension and uremia .
Historically, the prognosis for patients with aHUS was poor and in the pre-eculizumab era at 3–5 years after onset, 36–48% [22, 37] of children and 64–67%,  of adults had died or reached ESRD. The underlying genetic cause predicted the outcome of disease with those carrying CD46 mutations having the best prognosis (3 year renal survival 94%). In individuals with CFH mutations, up to 77% of patients had developed ESRD or had died at 3–5 years. Only 30–40% of individuals with CFI and C3 mutations will be alive with native kidney function at 3–5 years, [4, 37]. In those with FH-autoantibodies, 36.5–63% die or reach ESRD over a similar timescale.
The outcome following renal transplantation was also poor and again the outcome was predicted largely by the underlying genetic abnormality. The overall recurrence was 68% and 5-year death-censored graft survival 51% with highest risk associated with CFH, CFB, and C3 mutations and the lowest with CD46 mutations. [38, 39]
The genetic mutations seen in complement-mediated aHUS are not causative but are instead predisposing, suggesting that additional genetic and environmental modifiers are important. Penetrance of disease is age related and has been reported to be as high as 64% by the age of 70 for individuals carrying a single genetic mutation . A small proportion of aHUS patients (~ 3%) will have more than one mutation with increased penetrance per additional mutation . Risk haplotypes have also been shown to increase disease penetrance. Even where an individual has multiple genetic risk factors, a trigger is frequently required (e.g., infections , pregnancy ) to unmask a latent complement defect. These triggers usually activate complement: complement activation is the normal physiological response to infection and occurs in the placenta in normal pregnancy.
Eculizumab in aHUS
The elucidation of the role of complement in disease provided the rationale for the use of eculizumab in complement-mediated aHUS. Eculizumab, a recombinant humanized monoclonal antibody directed against C5, blocks the cleavage of C5 into its effector components C5a and C5b. Landmark studies in primary aHUS published in 2013 demonstrated its efficacy which have been replicated in subsequent extension studies , prospective (non-randomized) studies [44, 45], and cohort analysis . The role of eculizumab in secondary aHUS remains to be established (reviewed ).
The optimal length of treatment with eculizumab for individuals presenting with complement-mediated aHUS is unclear although the current license for eculizumab is for lifelong treatment; eculizumab withdrawal has been reported in a large series of aHUS patients with relapse reported in around one third of patients, all carrying complement mutations . In those patients experiencing a relapse post withdrawal, rapid reintroduction of complement inhibition normalized the renal function. This suggests that a disease-driven intermittent regime could be used although prospective trials are required.
Eculizumab non-responsive aHUS
There is no biomarker currently that will confirm the diagnosis of a primary complement-mediated aHUS in the acute setting, and the diagnosis is therefore one of exclusion. As early initiation of eculizumab has been shown to lead to better outcomes, treatment is often commenced in patients with suspected primary complement-mediated aHUS, and discontinued if an alternative etiology is subsequently identified. With the increasing use of eculizumab in clinical practice, it has become apparent that there are subgroups of aHUS that do not respond to eculizumab. In the recent pediatric trial, Greenbaum et al. highlighted that for those with a rare genetic variant in the complement system or an autoantibody to FH, all had an improvement in estimated glomerular filtration rate (eGFR), while 27% of individuals without an identified complement abnormality failed to show an improvement . It is not clear whether this represents late presentation of disease or true non-response.
More recently, individuals presenting with a TMA with failure to respond to eculizumab have been demonstrated to have genetic variants in the non-complement genes DGKE , INF2 , and MMACHC .
Diacylglycerol kinase epsilon (DGKE) is a lipid kinase that catalyzes the phosphorylation of diacylglycerol substrates (DAGs) to phosphatidic acid. Recessive mutations causing aHUS were first reported in 2013 . The exact mechanisms resulting in the TMA are yet to be fully elucidated; however, loss of DGKE function results in enhanced signaling through arachidonic acid-containing DAGs (AADAGs) and enhanced activation of PKC (protein kinase C). In the endothelium, PKC activation results in upregulation of prothrombotic factors and the downregulation of VEGFR2 signaling and these may play a role.
Only a small number of cases have been published, but it appears to present aged < 1 year and commonly results in progressive chronic kidney disease (CKD) and ESRF . There is insufficient evidence to determine optimal management; there are reports of both response and non-response to eculizumab. Concomitant mutations in complement genes have been reported. Genetic pleiotropy is seen: DGKE mutations have also been associated with mesangioproliferative glomerulonephritis (MPGN)  .
Inverted formin 2
Mutations in inverted formin 2 (INF2) have recently been reported in families with TMAs which was non-responsive to eculizumab . INF2 is a ubiquitously expressed formin protein which accelerates actin polymerization and depolymerization, thus regulating a range of cytoskeleton dependent cellular functions including the secretory pathway. As with DGKE, genetic pleiotropism is also seen with most individuals with INF2 mutations presenting with focal segmental glomerulosclerosis (FSGS) and nephrotic syndrome. It remains to be seen whether this is a primary aHUS or secondary phenomenon in association with FSGS.
Methylmalonic aciduria and homocystinuria, cobalamin C (cblC) type
Homozygous or compound heterozygous mutations in the MMACHC gene result in a disorder of cobalamin (cbl; vitamin B12) metabolism that causes aHUS. Although the pathophysiologic mechanisms that result in endothelial damage are unclear, metabolic therapy with hydroxycobalamin is very effective at preventing disease. It appears that MMACHC-mediated aHUS is complement independent as the small number of published reports of eculizumab use describe non-response .
Polymorphisms in C5 and the use of Coversin to treat TMA
A rare polymorphism in C5 (p.R885H) has been reported in the Japanese population which prevented eculizumab binding . More recently, a European with a functionally significant CFH mutation (p.D1119G) and a TMA post-bone marrow transplant was shown to carry this SNP preventing the use of eculizumab . In this case, an alternative C5 inhibitor, Coversin, was used. This is a recombinant protein derived from the tick, Ornithodoros moubata. As this binds to a different epitope on C5, this completely blocked the terminal pathway and there appeared to be a clinical response although there was a limited supply of the drug and the patient died .
C3 glomerulopathy (C3G) is a recently identified pathological entity describing a group of diseases in which uncontrolled complement activation can lead to complement deposition within the glomerulus . Historically, uncontrolled complement activation has been associated with the disease, membranoproliferative glomerulonephritis (MPGN) [55, 56]. These diseases are ultra-rare, affecting ~ 1 per million population [57,58,59].
Classification and pathology of C3G
The classification of diseases in uncontrolled complement activation resulting in glomerulopathy continues to evolve. The term C3G was introduced to alert the clinician to the possibility of an underlying abnormality of the complement system . C3G can be further classified by the pattern of dense deposits on electron microscopy. Dense deposit disease (DDD) is a specific form of C3G that is classified by the presence of dense osmiophilic intramembranous deposits seen on electron microscopy. C3 glomerulonephritis (C3GN) are forms of C3G in which deposits on electron microscopy may be light dense, amorphous mesangial, paramesangial, subendothelial, or subepithelial.
A diagnosis of C3G requires a renal biopsy. The presence of C3 dominant staining on immunofluorescence (IF), with an intensity of at least two orders of magnitude greater than any other immunoreactant (IgG, IgM, IgA, and C1q) provides the best sensitivity and specificity for C3G . This current definition of C3G captures about 90% of cases of DDD, and possibly fewer cases of C3GN . Once C3G has been diagnosed on renal biopsy, light microscopy then identifies diverse patterns of glomerular injury that include MPGN [54, 60], and detects additional features such as crescentic disease or markers of chronic disease such as interstitial fibrosis and tubular atrophy.
MPGN is a pattern of glomerular injury characterized by the presence of mesangial expansion, cellular proliferation, and double-contouring of the glomerular basement membrane . The classification of MPGN was historically based upon the position of electron dense deposits relative to the glomerular basement membrane. Three types of MPGN were defined in this manner, type 1 (subendothelial), type 2 or DDD (intramembranous), and type 3 (subendothelial and subepithelial) . Type 1 and type 3 MPGN typically stained positive for immunoglobulins and C3 on IF whereas type 2 MPGN typically stained for C3 only. MPGN of all types were previously associated with uncontrolled complement activation.
Overlap of C3G and MPGN
The classifications of C3G and MPGN overlap . The new classification of C3G includes cases of MPGN that were previously classified as type 1, 2, or 3. Furthermore, the definition of C3G identifies cases without MPGN, in which uncontrolled complement activation might not have been recognized . Evidence of uncontrolled complement activation continues to be found in cases of MPGN that do not meet the diagnostic criteria of C3G [65,66,67]. Currently, these cases are termed immune-complex MPGN. Therefore, suspicion of uncontrolled complement activation should include the current definition of C3G and an overlap with cases of immune-complex MPGN (Fig. 2).
Although uncontrolled complement activation may result in immune-complex MPGN, other secondary causes of MPGN should also be considered. These causes are summarized . Treatment can then be directed at the secondary cause.
Monoclonal gammopathy of renal significance
The absence of immunoglobulin on renal biopsy (in the setting of C3 deposition) is the hallmark of a diagnosis of C3G, usually indicative of an underlying disorder of complement regulation. However, it is increasingly recognized that deposition of monotypic immunoglobulin may be masked , and only identified following pronase digest. Upon identification of monoclonal deposits on the renal biopsy, the possibility of a monoclonal gammopathy needs to be considered. Treatment of these conditions is usually directed at the cause of the monoclonal gammopathy .
Complement derangement in C3G and MPGN
A range of acquired and inherited abnormalities have been described as a cause of complement dysregulation in cases of C3G and MPGN. Unlike in aHUS, these abnormalities tend to result in fluid phase dysregulation of AP and acquired abnormalities predominate.
FH deficiency leads to uncontrolled activation of AP in the fluid phase [71, 72] and causes MPGN and C3G [56, 64, 73]. Genetic causes of FH deficiency are summarized in Table 2. Briefly, FH deficiency can be quantitative and due to mutations in CFH, inherited in homozygosity or heterozygosity, resulting in complete or partial FH deficiency, respectively. Other pathogenic mutations in CFH lead to a functional deficiency of FH due to the expression of proteins that have defective binding to C3b resulting in impairment of fluid phase complement regulation [80, 81, 83]. Overall, the prevalence of rare genetic variants in these cohorts ranges from 4 to 16.2% of patients [65, 66, 87]. The functional significance of a number of other rare genetic variants reported in these case series of MPGN or C3G is not known (Table 2). 
Recent studies suggest an important role of FHR proteins in complement regulation. FHR proteins may compete with FH for C3b binding and prevent the regulatory activities of FH on surface-bound C3b . SCR1 and 2 of FHR1, 2, and 5 have a very high degree of sequence homology (Fig. 3) and share a dimerization motif. These studies show that these FHR proteins exist in dimeric form. FHR proteins do not have complement regulatory domains and as a result, dimeric forms of FHRs with high avidity to C3b act as competitive antagonists, preventing the normal regulatory function of FH and therefore “deregulating FH” .
Genomic abnormalities in C3G
First identified in a large Cypriot pedigree , a number of genomic abnormalities in the RCA cluster have been described in familial cases of C3G (Table 3). In all cases, the genomic abnormality resulted in the formation of a larger CFHR gene resulting in FHR proteins with additional SCRs [97,98,99,100,101,102,103,104,105]. Functional study of dimeric forms of abnormal FHR proteins demonstrated an enhanced ability to compete with FH resulting in enhanced deregulation of FH as a possible mechanism of disease [97, 102]. In the case of the FHR2-FHR5 hybrid protein reported by Chen et al., functional studies showed evidence of stabilization of C3bBb in the presence of the hybrid FHR2-FHR5 protein resulting in complement activation in the fluid phase  and a possible role in binding properdin .
Complement factor I and membrane cofactor
Rare genetic variants in other complement regulators (CFI and CD46) are infrequently identified in C3G and MPGN (Table 2). Reported variants have all been inherited in heterozygosity. A few (resulting in low FI levels [65, 89, 90]) are pathogenic but their importance in disease pathogenesis has not been established.
Components of the AP C3 convertase—C3 and FB
Detailed functional studies of several familial rare genetic variants in C3 in C3G have been described. In a case of familial DDD, the variant Δ923-924DG does not undergo conformational change to C3b but does form a C3 convertase that is resistant to decay by FH . In a report of familial C3GN, the variant I756T results in defective C3b inactivation by FI in setting of cofactors CR1 and FH .
Rare genetic variants in C3 and CFB have also been described in cohorts of C3G and MPGN   and includes the S367R variant in CFB in one familial case of C3GN . Most of these variants have not been functionally studied (Table 2).
Common genetic susceptibility factors have been reported in MPGN and C3G. In DDD, the Y402H polymorphism in CFH [65, 107, 108] associates with an increased risk of disease. Conversely, the V62I polymorphism was shown to be protective against DDD [26, 66].
Risk haplotypes in CFH also associate with disease. The H1 haplotype that carries the at-risk Y402H SNP in DDD associates with an increased risk of DDD [26, 107]. The H2 haplotype that carries the protective SNP V62I was shown to be protective in DDD .
Common SNPs and haplotypes in CD46 have been studied in cohorts of C3G and MPGN. The intronic SNP c.-652G was protective in MPGN and C3GN. This association was also observed in cases of MPGN type 1 and C3GN, in which the haplotype CD46AAGGT was observed more frequently, while the haplotype CD46GAGGT was observed less frequently . These findings were not observed in a later study . In this later study, the SNPs c.-366A>G and c. *783 T>C were observed more frequently in immune-complex MPGN than controls . In the same later study, the SNP c.-366A was observed more frequently in DDD compared to controls .
Several common SNPs in C3 and CFB have been studied in C3G and MPGN. The SNPs, R102G [108, 109], and P314L in C3 are associated with DDD . The SNPs in CFB, R32W, and R32Q were not associated with C3G or MPGN .
Acquired abnormalities in C3G and MPGN
The first acquired abnormality discovered in MPGN was a circulating factor in serum that was found to increase cell lysis in the fluid phase . This was later discovered to be IgG that stabilized C3bBb by 10-fold [110, 111] now known as C3 nephritic factor. There is a strong association of C3 nephritic factor with all forms of C3G and MPGN, and is prevalent in up to 80% of DDD and 50% of MPGN and C3GN [65, 78]. C3 nephritic factors are not specific to MPGN and C3G and have been observed in acquired partial lipodystrophy  and in normal individuals .
Autoantibodies to individual complement components and their regulators have been reported in cases of C3G and MPGN. Autoantibodies to FB were first described in DDD [78, 114]. In one patient, these were shown to stabilize C3bBb, causing C3 consumption and terminal pathway activation . No functional data are available in a further report in which three DDD patients with autoantibodies to FB are described . Autoantibodies to C3b and FB in the same patient were described in two cases of DDD. These patients lacked C3 nephritic factor but the antibodies enhanced C3bBb activity . Autoantibodies in FB and C3b have recently been reported in a cohort of C3G and MPGN . Functional studies of purified IgG from patients in this cohort also result in AP activation.
Autoantibodies to FH have also been described in patients with C3G and MPGN. These bind predominantly to the N-terminal domain of FH and impair the regulatory activity of FH [78, 116]. The prevalence of autoantibodies to FH was 11% in a MPGN/C3G cohort . In this cohort, patients with autoantibodies to FH did not associate with homozygous deletion of CFHR3/1. These autoantibodies associated with C3 nephritic factor in children and monoclonal gammopathy in adults . The association of autoantibodies to FH and monoclonal gammopathy had been previously described in case reports [118, 119].
Clinical presentation and outcome of C3G and MPGN
MPGN and C3G, especially the subset of patients with DDD, are typically diseases of childhood and young adulthood [57, 65]. They present with similar clinical features that include proteinuria, hematuria, and renal failure [57, 65]. Renal failure is progressive and 40% of patients develop end-stage renal disease (ESRD) at 10 years [57, 65, 120]. Recurrence in transplantation is common in all types, ranging from 30 to 40% in MPGN type 1 to 80–90% in DDD . Plasma C3 levels are often low [57, 65, 66, 122]. Individual complement abnormalities have not been associated with a greater risk of adverse outcomes [57, 65] although the absence of a C3 nephritic factor or a rare genetic variant did have a higher risk of progression to ESRD in an Italian cohort .
The clinical features of patients with FHR5 nephropathy, a subset of patients with C3G, differ from other forms of C3G. First reported in large pedigrees with Cypriot ancestry, these patients often have Synpharyngitic hematuria. Prognosis is often worse in males with FHR5 nephropathy .
Treatments in C3G and MPGN
There are no universally effective treatments for C3G or MPGN. The only double blind randomized control trial in this group of patients was performed in 1992 . Eighty children (with MPGN types 1, 2, and 3) were randomized to receive 40 mg/m2 of prednisolone on alternate days. In this study, long-term treatment with prednisolone did appear to improve the outcome of patients with MPGN. Other studies suggest some benefit from the use of cyclophosphamide , mycophenolate mofetil (MMF) [128, 129] and the combination of aspirin and dipyridamole [130,131,132]. The use of rituximab has been described in case reports only [133,134,135].
Unlike in aHUS, the role of complement inhibition in C3G and MPGN is not clear, despite the role of uncontrolled complement activation in disease. To date, there is one clinical trial of eculizumab in MPGN that is currently underway . Nonetheless, eculizumab use has been reported in a growing number of cases of C3G and MPGN. Current reports suggest a more beneficial role for eculizumab in cases where prominent terminal pathway activity is seen [137,138,139,140,141].
Other reported therapies that modulate complement include the replacement of FH in patients with a functional deficiency of FH using plasma exchange  and soluble CR1 . Further studies are required to determine whether complement inhibition in C3G can be effective.
Paroxysmal nocturnal hemoglobinuria
Paroxysmal nocturnal hemoglobinuria (PNH) is a rare hemolytic anemia first described in 1882 . In addition to hemolysis, thrombosis, muscle dystonias, chronic kidney disease, and bone marrow failure may occur . The incidence of PNH is ~ 1–1.5 cases per million individuals worldwide . Most patients present between the ages of 30–59  and it is rare in children .
Unlike the germline mutations described commonly in aHUS and less commonly in C3G, PNH is caused by somatic mutations in the phosphatidylinositol glycan anchor biosynthesis class A gene (PIGA) in one or more long-lasting hematopoietic stem cell (HSC) clones [148,149,150]. The majority of mutations seen are indels resulting in frameshifts [151, 152]. PIGA’s location on the X chromosome accounts for the ability of one somatic mutation to cause PNH as only one allele is functional in men and women.
The expansion of PIGA-deficient HSC clones is central to the clinical phenotype of PNH; however, the PIGA mutations do not themselves confer a growth advantage [153, 154]. Both intrinsic (additive genetic and epigenetic variations ) and extrinsic (bone marrow failure ) clonal mechanisms have been suggested to account for the clonal expansion (reviewed ).
Although there are multiple genes involved in GPI synthesis, there is only one case of PNH reported where PIGA mutations were not seen. In this case, one somatic mutation in addition to a germline mutation in PIGT caused lack of GPI anchored cells and the PNH phenotype [157, 158].
PIGA encodes for a glycosyl transferase that is required in the biosynthetic pathway for the synthesis of glycosyl phosphatidylinositol (GPI) . PIGA mutations lead to a deficiency of GPI-anchored proteins including CD14, CD16b, CD48, and the complement inhibitor proteins CD55 (decay accelerating factor; DAF) and CD59.
CD55 accelerates the decay of the alternative and classical pathway C3 and C5 convertases while CD59 is a terminal pathway regulator which binds C8 preventing C9 recruitment and formation of the membrane attack complex. Deficiency of these complement regulators is critical to PNH erythrocytes being susceptible to complement-mediated attack.
In addition to the dominant hemolytic clinical feature of PNH, thrombosis is commonly seen. The exact mechanisms of thrombosis in PNH are unclear (reviewed by Hill et al. ) although the interplay of the complement and coagulation cascades, particularly C5 receptor signaling pathways, activation of platelets and intravascular hemolysis have been suggested.
Clinical presentation and outcome
In PNH-affected erythrocytes, the constant activation of the AP causes a chronic low-level hemolysis and at time of infections or other complement triggering events there may be a hemolytic attack . The most common cause of mortality of PNH is thromboembolism, with venous thrombosis more common than arterial thrombosis . Smooth muscle dystonias including back pain, abdominal pain, erectile dysfunction, and dysphagia are seen . Chronic kidney disease can occur with hemosiderin deposition leading to tubulointerstitial inflammation [163, 164]. Bone marrow failure is commonly seen in PNH but is not a consequence of the somatic mutations in PIGA .
Historically, the median survival of patients with PNH was approximately 10 years [165,166,167]; however, since the introduction of eculizumab, in those without bone marrow failure, a normal lifespan can be expected [146, 168].
Eculizumab in PNH
Eculizumab is currently the only licensed therapy for PNH. Its introduction resulted in improvement in intravascular hemolysis [169, 170], thrombosis , renal function , and survival . Variable response to treatment is seen with some patients presenting with residual hemolysis and requiring red blood cell transfusions. Low-level extravascular hemolysis is seen in most PNH patients on eculizumab. In this setting, C3 fragments opsonizing erythrocytes are recognized by macrophages in the spleen and liver resulting in their destruction . It has recently been shown that a polymorphism in Complement receptor 1 (CR1) alters the level of CR1 on erythrocytes and consequently the level of C3 opsonization of erythrocytes . This increases the clearance of the erythrocytes.
As seen in aHUS, a polymorphism in C5 can limit eculizumab’s effectiveness and complete blockage should be confirmed (AH50/CH50/sC5b-9) .
Novel complement inhibitors in PNH
Several novel complement inhibitors are in various stages of development for the treatment of PNH including the C5 inhibitors ALXN1210 (Alexion; NCT02946463, NCT03056040), RA101495 (RaPharma NCT03030183, NCT03078582), ALNCC5 (NCT02352493 Alnylam), Coversin (NCT02591862; Akari), the C3 inhibitor compstatin analogue APL-2 (NCT02588833; Apellis), and the factor D inhibitor ACH-4471 (Achillion). These are reviewed in more detail in this issue by Harris .
Together, these classical diseases of complement dysregulation provide a window on the vastly different phenotypes that can result from the subtle variations in complement regulation. These diseases will provide the test bed for the next generation of complement inhibitory agents.
Brocklebank V, Kavanagh D. 2017 Thrombotic microangiopathy and the kidney. Clin J Am Soc Nephrol;in press: https://doi.org/10.2215/CJN.00620117
Goodship TH, Cook HT, Fakhouri F, Fervenza FC, Fremeaux-Bacchi V, Kavanagh D et al (2017) Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a “Kidney Disease: Improving Global Outcomes” (KDIGO) Controversies Conference. Kidney Int 91:539–551
Warwicker P, Goodship TH, Donne RL, Pirson Y, Nicholls A, Ward RM et al (1998) Genetic studies into inherited and sporadic hemolytic uremic syndrome. Kidney Int 53:836–844
Kavanagh D, Goodship TH, Richards A (2013) Atypical hemolytic uremic syndrome. Semin Nephrol 33:508–530
Richards A, Kavanagh D, Atkinson JP (2007) Inherited complement regulatory protein deficiency predisposes to human disease in acute injury and chronic inflammatory states the examples of vascular damage in atypical hemolytic uremic syndrome and debris accumulation in age-related macular degeneration. Adv Immunol 96:141–177
Schmidt CQ, Herbert AP, Kavanagh D, Gandy C, Fenton CJ, Blaum BS et al (2008) A new map of glycosaminoglycan and C3b binding sites on factor H. J Immunol 181:2610–2619
Blaum BS, Hannan JP, Herbert AP, Kavanagh D, Uhrin D, Stehle T (2015) Structural basis for sialic acid-mediated self-recognition by complement factor H. Nat Chem Biol 11:77–82
Morgan HP, Schmidt CQ, Guariento M, Blaum BS, Gillespie D, Herbert AP et al (2011) Structural basis for engagement by complement factor H of C3b on a self surface. Nat Struct Mol Biol 18:463–470
Ferreira VP, Herbert AP, Cortes C, McKee KA, Blaum BS, Esswein ST et al (2009) The binding of factor H to a complex of physiological polyanions and C3b on cells is impaired in atypical hemolytic uremic syndrome. J Immunol 182:7009–7018
Lehtinen MJ, Rops AL, Isenman DE, van der Vlag J, Jokiranta TS (2009) Mutations of factor H impair regulation of surface-bound C3b by three mechanisms in atypical hemolytic uremic syndrome. J Biol Chem 284:15650–15658
Heinen S, Sanchez-Corral P, Jackson MS, Strain L, Goodship JA, Kemp EJ et al (2006) De novo gene conversion in the RCA gene cluster (1q32) causes mutations in complement factor H associated with atypical hemolytic uremic syndrome. Hum Mutat 27:292–293
Venables JP, Strain L, Routledge D, Bourn D, Powell HM, Warwicker P et al (2006) Atypical haemolytic uraemic syndrome associated with a hybrid complement gene. PLoS Med 3:e431
Francis NJ, McNicholas B, Awan A, Waldron M, Reddan D, Sadlier D et al (2012) A novel hybrid CFH/CFHR3 gene generated by a microhomology-mediated deletion in familial atypical hemolytic uremic syndrome. Blood 119:591–601
Challis RC, Araujo GS, Wong EK, Anderson HE, Awan A, Dorman AM et al (2016) A de novo deletion in the regulators of complement activation cluster producing a hybrid complement factor H/complement factor H-related 3 gene in atypical hemolytic uremic syndrome. J Am Soc Nephrol 27:1617–1624
Richards A, Kathryn Liszewski M, Kavanagh D, Fang CJ, Moulton E, Fremeaux-Bacchi V et al (2007) Implications of the initial mutations in membrane cofactor protein (MCP; CD46) leading to atypical hemolytic uremic syndrome. Mol Immunol 44:111–122
Kavanagh D, Kemp EJ, Mayland E, Winney RJ, Duffield JS, Warwick G et al (2005) Mutations in complement factor I predispose to development of atypical hemolytic uremic syndrome. J Am Soc Nephrol 16:2150–2155
Fremeaux-Bacchi V, Miller EC, Liszewski MK, Strain L, Blouin J, Brown AL et al (2008) Mutations in complement C3 predispose to development of atypical hemolytic uremic syndrome. Blood 112:4948–4952
Sartz L, Olin AI, Kristoffersson AC, Stahl AL, Johansson ME, Westman K et al (2012) A novel C3 mutation causing increased formation of the C3 convertase in familial atypical hemolytic uremic syndrome. J Immunol 188:2030–2037
Roumenina LT, Jablonski M, Hue C, Blouin J, Dimitrov JD, Dragon-Durey MA et al (2009) Hyperfunctional C3 convertase leads to complement deposition on endothelial cells and contributes to atypical hemolytic uremic syndrome. Blood 114:2837–2845
Goicoechea de Jorge E, Harris CL, Esparza-Gordillo J, Carreras L, Arranz EA, Garrido CA et al (2007) Gain-of-function mutations in complement factor B are associated with atypical hemolytic uremic syndrome. Proc Natl Acad Sci U S A 104:240–245
Delvaeye M, Noris M, De Vriese A, Esmon CT, Esmon NL, Ferrell G et al (2009) Thrombomodulin mutations in atypical hemolytic-uremic syndrome. N Engl J Med 361:345–357
Fremeaux-Bacchi V, Fakhouri F, Garnier A, Bienaime F, Dragon-Durey MA, Ngo S et al (2013) Genetics and outcome of atypical hemolytic uremic syndrome: a nationwide French series comparing children and adults. Clin J Am Soc Nephrol 8:554–562
Fremeaux-Bacchi V, Kemp EJ, Goodship JA, Dragon-Durey MA, Strain L, Loirat C et al (2005) The development of atypical haemolytic-uraemic syndrome is influenced by susceptibility factors in factor H and membrane cofactor protein: evidence from two independent cohorts. J Med Genet 42:852–856
Esparza-Gordillo J, Goicoechea de Jorge E, Buil A, Carreras Berges L, Lopez-Trascasa M, Sanchez-Corral P et al (2005) Predisposition to atypical hemolytic uremic syndrome involves the concurrence of different susceptibility alleles in the regulators of complement activation gene cluster in 1q32. Hum Mol Genet 14:703–712
Frimat M, Roumenina L, Tabarin F, Halbwachs-Mecarelli L, Fremeaux-Bacchi V (2012) Membrane cofactor protein (MCP) haplotype, which predisposes to atypical hemolytic and uremic syndrome, has no consequence on neutrophils and endothelial cells MCP levels or on HUVECs ability to activate complement. Immunobiology 217:1187–1188
Pickering MC, de Jorge EG, Martinez-Barricarte R, Recalde S, Garcia-Layana A, Rose KL et al (2007) Spontaneous hemolytic uremic syndrome triggered by complement factor H lacking surface recognition domains. J Exp Med 204:1249–1256
Pechtl IC, Kavanagh D, McIntosh N, Harris CL, Barlow PN (2011) Disease-associated N-terminal complement factor H mutations perturb cofactor and decay-accelerating activities. J Biol Chem 286:11082–11090
Tortajada A, Montes T, Martinez-Barricarte R, Morgan BP, Harris CL, de Cordoba SR (2009) The disease-protective complement factor H allotypic variant Ile62 shows increased binding affinity for C3b and enhanced cofactor activity. Hum Mol Genet 18:3452–3461
Dragon-Durey MA, Loirat C, Cloarec S, Macher MA, Blouin J, Nivet H et al (2005) Anti-factor H autoantibodies associated with atypical hemolytic uremic syndrome. J Am Soc Nephrol: JASN 16:555–563
Brocklebank V, Johnson S, Sheerin TP, Marks SD, Gilbert RD, Tyerman K et al (2017) Factor H autoantibody is associated with atypical hemolytic uremic syndrome in children in the United Kingdom and Ireland. Kidney Int 92:1261–1271
Jozsi M, Licht C, Strobel S, Zipfel SL, Richter H, Heinen S et al (2008) Factor H autoantibodies in atypical hemolytic uremic syndrome correlate with CFHR1/CFHR3 deficiency. Blood 111:1512–1514
Moore I, Strain L, Pappworth I, Kavanagh D, Barlow PN, Herbert AP et al (2010) Association of factor H autoantibodies with deletions of CFHR1, CFHR3, CFHR4, and with mutations in CFH, CFI, CD46, and C3 in patients with atypical hemolytic uremic syndrome. Blood 115:379–387
Jozsi M, Strobel S, Dahse HM, Liu WS, Hoyer PF, Oppermann M et al (2007) Anti factor H autoantibodies block C-terminal recognition function of factor H in hemolytic uremic syndrome. Blood 110:1516–1518
Blanc C, Roumenina LT, Ashraf Y, Hyvarinen S, Sethi SK, Ranchin B et al (2012) Overall neutralization of complement factor H by autoantibodies in the acute phase of the autoimmune form of atypical hemolytic uremic syndrome. J Immunol 189:3528–3537
Kavanagh D, Pappworth IY, Anderson H, Hayes CM, Moore I, Hunze EM et al (2012) Factor I autoantibodies in patients with atypical hemolytic uremic syndrome: disease-associated or an epiphenomenon? Clin J Am Soc Nephrol 7:417–426
Sheerin NS, Kavanagh D, Goodship TH, Johnson S (2016) A national specialized service in England for atypical haemolytic uraemic syndrome-the first year’s experience. QJM 109:27–33
Noris M, Caprioli J, Bresin E, Mossali C, Pianetti G, Gamba S et al (2010) Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype. Clin J Am Soc Nephrol 5:1844–1859
Kavanagh D, Richards A, Goodship T, Jalanko H (2010) Transplantation in atypical hemolytic uremic syndrome. Semin Thromb Hemost 36:653–659
Le Quintrec M, Zuber J, Moulin B, Kamar N, Jablonski M, Lionet A et al (2013) Complement genes strongly predict recurrence and graft outcome in adult renal transplant recipients with atypical hemolytic and uremic syndrome. Am J Transplant 13:663–675
Bresin E, Rurali E, Caprioli J, Sanchez-Corral P, Fremeaux-Bacchi V, Rodriguez de Cordoba S et al (2013) Combined complement gene mutations in atypical hemolytic uremic syndrome influence clinical phenotype. J Am Soc Nephrol: JASN 24:475–486
Caprioli J, Noris M, Brioschi S, Pianetti G, Castelletti F, Bettinaglio P et al (2006) Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome. Blood 108:1267–1279
Bruel A, Kavanagh D, Noris M, Delmas Y, Wong EKS, Bresin E et al (2017) Hemolytic uremic syndrome in pregnancy and postpartum. Clin J Am Soc Nephrol 12:1237–1247
Licht C, Greenbaum LA, Muus P, Babu S, Bedrosian CL, Cohen DJ et al (2015) Efficacy and safety of eculizumab in atypical hemolytic uremic syndrome from 2-year extensions of phase 2 studies. Kidney Int 87:1061–1073
Fakhouri F, Hourmant M, Campistol JM, Cataland SR, Espinosa M, Gaber AO et al (2016) Terminal complement inhibitor eculizumab in adult patients with atypical hemolytic uremic syndrome: a single-arm, open-label trial. Am J Kidney Dis 68:84–93
Greenbaum LA, Fila M, Ardissino G, Al-Akash SI, Evans J, Henning P et al (2016) Eculizumab is a safe and effective treatment in pediatric patients with atypical hemolytic uremic syndrome. Kidney Int 89:701–711
Brocklebank V, Kavanagh D (2017) Complement C5 inhibiting therapy for the thrombotic microangiopathies: accumulating evidence, but not a panacea. Clin Kidney J 10:600–624
Fakhouri F, Fila M, Provot F, Delmas Y, Barbet C, Chatelet V et al (2017) Pathogenic variants in complement genes and risk of atypical hemolytic uremic syndrome relapse after eculizumab discontinuation. Clin J Am Soc Nephrol 12:50–59
Lemaire M, Fremeaux-Bacchi V, Schaefer F, Choi M, Tang WH, Le Quintrec M et al (2013) Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome. Nat Genet 45:531–536
Challis RC, Ring T, Xu Y, Wong EK, Flossmann O, Roberts IS et al (2017) Thrombotic microangiopathy in inverted formin 2-mediated renal disease. J Am Soc Nephrol 28:1084–1091
Beck BB, van Spronsen F, Diepstra A, Berger RM, Komhoff M (2017) Renal thrombotic microangiopathy in patients with cblC defect: review of an under-recognized entity. Pediatr Nephrol 32:733–741
Ozaltin F, Li B, Rauhauser A, An SW, Soylemezoglu O, Gonul II et al (2013) DGKE variants cause a glomerular microangiopathy that mimics membranoproliferative GN. J Am Soc Nephrol 24:377–384
Nishimura J, Yamamoto M, Hayashi S, Ohyashiki K, Ando K, Brodsky AL et al (2014) Genetic variants in C5 and poor response to eculizumab. N Engl J Med 370:632–639
Goodship T, Pinto F, Weston-Davies W, Silva J, Nishimura J, Nunn M et al (2017) Use of the complement inhibitor coversin to treat HSCT-associated TMA. Blood Adv 1:1254–1258
Pickering MC, D'Agati VD, Nester CM, Smith RJ, Haas M, Appel GB et al (2013) C3 glomerulopathy: consensus report. Kidney Int 84:1079–1089
Spitzer RE, Vallota EH, Forristal J, Sudora E, Stitzel A, Davis NC et al (1969) Serum C’3 lytic system in patients with glomerulonephritis. Science 164:436–437
Levy M, Halbwachs-Mecarelli L, Gubler MC, Kohout G, Bensenouci A, Niaudet P et al (1986) H deficiency in two brothers with atypical dense intramembranous deposit disease. Kidney Int 30:949–956
Medjeral-Thomas NR, O'Shaughnessy MM, O’Regan JA, Traynor C, Flanagan M, Wong L et al (2014) C3 glomerulopathy: clinicopathologic features and predictors of outcome. Clin J Am Soc Nephrol: CJASN 9:46–53
Briganti EM, Dowling J, Finlay M, Hill PA, Jones CL, Kincaid-Smith PS et al (2001) The incidence of biopsy-proven glomerulonephritis in Australia. Nephrol Dial Transplant 16:1364–1367
West CD (1992) Idiopathic membranoproliferative glomerulonephritis in childhood. Pediatr Nephrol 6:96–103
Hou J, Markowitz GS, Bomback AS, Appel GB, Herlitz LC, Barry Stokes M et al (2014) Toward a working definition of C3 glomerulopathy by immunofluorescence. Kidney Int 85:450–456
Sethi S, Fervenza FC (2012) Membranoproliferative glomerulonephritis—a new look at an old entity. N Engl J Med 366:1119–1131
Anders D, Thoenes W (1975) Basement membrane-changes in membranoproliferative glomerulonephritis: a light and electron microscopic study. Virchows Arch A Pathol Anat Histol 369:87–109
Sethi S, Nester CM, Smith RJ (2012) Membranoproliferative glomerulonephritis and C3 glomerulopathy: resolving the confusion. Kidney Int 81:434–441
Servais A, Fremeaux-Bacchi V, Lequintrec M, Salomon R, Blouin J, Knebelmann B et al (2007) Primary glomerulonephritis with isolated C3 deposits: a new entity which shares common genetic risk factors with haemolytic uraemic syndrome. J Med Genet 44:193–199
Servais A, Noel LH, Roumenina LT, Le Quintrec M, Ngo S, Dragon-Durey MA et al (2012) Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies. Kidney Int 82:454–464
Iatropoulos P, Noris M, Mele C, Piras R, Valoti E, Bresin E et al (2016) Complement gene variants determine the risk of immunoglobulin-associated MPGN and C3 glomerulopathy and predict long-term renal outcome. Mol Immunol 71:131–142
Marinozzi MC, Roumenina LT, Chauvet S, Hertig A, Bertrand D, Olagne J et al (2017) Anti-factor B and anti-C3b autoantibodies in C3 glomerulopathy and Ig-associated membranoproliferative GN. J Am Soc Nephrol: JASN 28:1603–1613
Masani N, Jhaveri KD, Fishbane S (2014) Update on membranoproliferative GN. Clin J Am Soc Nephrol: CJASN 9:600–608
Larsen CP, Messias NC, Walker PD, Fidler ME, Cornell LD, Hernandez LH et al (2015) Membranoproliferative glomerulonephritis with masked monotypic immunoglobulin deposits. Kidney Int 88:867–873
Chauvet S, Fremeaux-Bacchi V, Petitprez F, Karras A, Daniel L, Burtey S et al (2017) Treatment of B-cell disorder improves renal outcome of patients with monoclonal gammopathy-associated C3 glomerulopathy. Blood 129:1437–1447
Thompson RA, Winterborn MH (1981) Hypocomplementaemia due to a genetic deficiency of beta 1H globulin. Clin Exp Immunol 46:110–119
Pickering MC, Cook HT, Warren J, Bygrave AE, Moss J, Walport MJ et al (2002) Uncontrolled C3 activation causes membranoproliferative glomerulonephritis in mice deficient in complement factor H. Nat Genet 31:424–428
Dragon-Durey MA, Fremeaux-Bacchi V, Loirat C, Blouin J, Niaudet P, Deschenes G et al (2004) Heterozygous and homozygous factor h deficiencies associated with hemolytic uremic syndrome or membranoproliferative glomerulonephritis: report and genetic analysis of 16 cases. J Am Soc Nephrol 15:787–795
Alfandary H, Davidovits M (2015) Novel factor H mutation associated with familial membranoproliferative glomerulonephritis type I. Pediatr Nephrol 30:2129–2134
Vaziri-Sani F, Holmberg L, Sjoholm AG, Kristoffersson AC, Manea M, Fremeaux-Bacchi V et al (2006) Phenotypic expression of factor H mutations in patients with atypical hemolytic uremic syndrome. Kidney Int 69:981–988
Boyer O, Noel LH, Balzamo E, Guest G, Biebuyck N, Charbit M et al (2008) Complement factor H deficiency and posttransplantation glomerulonephritis with isolated C3 deposits. Am J Kidney Dis: Off J Natl Kidney Found 51:671–677
Gnappi E, Allinovi M, Vaglio A, Bresin E, Sorosina A, Pilato FP et al (2012) Membrano-proliferative glomerulonephritis, atypical hemolytic uremic syndrome, and a new complement factor H mutation: report of a case. Pediatr Nephrol 27:1995–1999
Zhang Y, Meyer NC, Wang K, Nishimura C, Frees K, Jones M et al (2012) Causes of alternative pathway dysregulation in dense deposit disease. Clin J Am Soc Nephrol: CJASN 7:265–274
Sethi S, Fervenza FC, Zhang Y, Zand L, Vrana JA, Nasr SH et al (2012) C3 glomerulonephritis: clinicopathological findings, complement abnormalities, glomerular proteomic profile, treatment, and follow-up. Kidney Int 82:465–473
Licht C, Heinen S, Jozsi M, Loschmann I, Saunders RE, Perkins SJ et al (2006) Deletion of Lys224 in regulatory domain 4 of factor H reveals a novel pathomechanism for dense deposit disease (MPGN II). Kidney Int 70:42–50
Yu Y, Triebwasser MP, Wong EK, Schramm EC, Thomas B, Reynolds R et al (2014) Whole-exome sequencing identifies rare, functional CFH variants in families with macular degeneration. Hum Mol Genet 23:5283–5293
Sethi S, Fervenza FC, Zhang Y, Nasr SH, Leung N, Vrana J et al (2011) Proliferative glomerulonephritis secondary to dysfunction of the alternative pathway of complement. Clin J Am Soc Nephrol: CJASN 6:1009–1017
Wong EK, Anderson HE, Herbert AP, Challis RC, Brown P, Reis GS et al (2014) Characterization of a factor H mutation that perturbs the alternative pathway of complement in a family with membranoproliferative GN. J Am Soc Nephrol: JASN 25:2425–2433
Martinez-Barricarte R, Heurich M, Valdes-Canedo F, Vazquez-Martul E, Torreira E, Montes T et al (2010) Human C3 mutation reveals a mechanism of dense deposit disease pathogenesis and provides insights into complement activation and regulation. J Clin Invest 120:3702–3712
Chauvet S, Roumenina LT, Bruneau S, Marinozzi MC, Rybkine T, Schramm EC et al (2015) A familial C3GN secondary to defective C3 regulation by complement receptor 1 and factor H. J Am Soc Nephrol 27:1665–1677
Janssen van Doorn K, Dirinck E, Verpooten GA, Couttenye MM (2013) Complement factor H mutation associated with membranoproliferative glomerulonephritis with transformation to atypical haemolytic uraemic syndrome. Clin Kidney J 6:216–219
Bu F, Borsa NG, Jones MB, Takanami E, Nishimura C, Hauer JJ et al (2015) High-throughput genetic testing for thrombotic microangiopathies and C3 glomerulopathies. J Am Soc Nephrol: JASN 27:1245–1253
Salmon JE, Heuser C, Triebwasser M, Liszewski MK, Kavanagh D, Roumenina L et al (2011) Mutations in complement regulatory proteins predispose to preeclampsia: a genetic analysis of the PROMISSE cohort. PLoS Med 8:e1001013
Bienaime F, Dragon-Durey MA, Regnier CH, Nilsson SC, Kwan WH, Blouin J et al (2010) Mutations in components of complement influence the outcome of factor I-associated atypical hemolytic uremic syndrome. Kidney Int 77:339–349
Kavanagh D, Yu Y, Schramm EC, Triebwasser M, Wagner EK, Raychaudhuri S et al (2015) Rare genetic variants in the CFI gene are associated with advanced age-related macular degeneration and commonly result in reduced serum factor I levels. Hum Mol Genet 24:3861–3870
Kavanagh D, Richards A, Noris M, Hauhart R, Liszewski MK, Karpman D et al (2008) Characterization of mutations in complement factor I (CFI) associated with hemolytic uremic syndrome. Mol Immunol 45:95–105
Nilsson SC, Kalchishkova N, Trouw LA, Fremeaux-Bacchi V, Villoutreix BO, Blom AM (2010) Mutations in complement factor I as found in atypical hemolytic uremic syndrome lead to either altered secretion or altered function of factor I. Eur J Immunol 40:172–185
Gleeson PJ, Wilson V, Cox TE, Sharma SD, Smith-Jackson K, Strain L et al (2016) Chromosomal rearrangement—a rare cause of complement factor I associated atypical haemolytic uraemic syndrome. Immunobiology 221:1124–1130
Nilsson SC, Karpman D, Vaziri-Sani F, Kristoffersson AC, Salomon R, Provot F et al (2007) A mutation in factor I that is associated with atypical hemolytic uremic syndrome does not affect the function of factor I in complement regulation. Mol Immunol 44:1835–1844
Imamura H, Konomoto T, Tanaka E, Hisano S, Yoshida Y, Fujimura Y et al (2015) Familial C3 glomerulonephritis associated with mutations in the gene for complement factor B. Nephrol Dial Transplant 30:862–864
Kavanagh D, Anderson HE (2012) Interpretation of genetic variants of uncertain significance in atypical hemolytic uremic syndrome. Kidney Int 81:11–13
Goicoechea de Jorge E, Caesar JJ, Malik TH, Patel M, Colledge M, Johnson S et al (2013) Dimerization of complement factor H-related proteins modulates complement activation in vivo. Proc Natl Acad Sci U S A 110:4685–4690
Gale DP, de Jorge EG, Cook HT, Martinez-Barricarte R, Hadjisavvas A, McLean AG et al (2010) Identification of a mutation in complement factor H-related protein 5 in patients of Cypriot origin with glomerulonephritis. Lancet 376:794–801
Chen Q, Wiesener M, Eberhardt HU, Hartmann A, Uzonyi B, Kirschfink M et al (2014) Complement factor H-related hybrid protein deregulates complement in dense deposit disease. J Clin Invest 124:145–155
Chen Q, Manzke M, Hartmann A, Buttner M, Amann K, Pauly D et al (2015) Complement factor H-related 5-hybrid proteins anchor properdin and activate complement at self-surfaces. J Am Soc Nephrol: JASN 27:1413–1425
Zhang Y, Xiao X, Garcia-Fernandez J, de Cordoba SR, Zipfel P, Meyer N et al (2013) A novel fusion gene CHFR5-CFHR2 causes C3 glomerulonephritis. Mol Immunol 56:297–297
Tortajada A, Yebenes H, Abarrategui-Garrido C, Anter J, Garcia-Fernandez JM, Martinez-Barricarte R et al (2013) C3 glomerulopathy-associated CFHR1 mutation alters FHR oligomerization and complement regulation. J Clin Invest 123:2434–2446
Malik TH, Lavin PJ, Goicoechea de Jorge E, Vernon KA, Rose KL, Patel MP et al (2012) A hybrid CFHR3-1 gene causes familial C3 glomerulopathy. J Am Soc Nephrol 23:1155–1160
Togarsimalemath SK, Sethi SK, Duggal R, Quintrec ML, Jha P, Daniel R et al (2017) A novel CFHR1-CFHR5 hybrid leads to a familial dominant C3 glomerulopathy. Kidney Int 92:876–887
Xiao X, Ghossein C, Tortajada A, Zhang Y, Meyer N, Jones M et al (2016) Familial C3 glomerulonephritis caused by a novel CFHR5-CFHR2 fusion gene. Mol Immunol 77:89–96
Besbas N, Gulhan B, Gucer S, Korkmaz E, Ozaltin F (2014) A novel CFHR5 mutation associated with C3 glomerulonephritis in a Turkish girl. J Nephrol 27:457–460
Abrera-Abeleda MA, Nishimura C, Smith JL, Sethi S, McRae JL, Murphy BF et al (2006) Variations in the complement regulatory genes factor H (CFH) and factor H related 5 (CFHR5) are associated with membranoproliferative glomerulonephritis type II (dense deposit disease). J Med Genet 43:582–589
Abrera-Abeleda MA, Nishimura C, Frees K, Jones M, Maga T, Katz LM et al (2011) Allelic variants of complement genes associated with dense deposit disease. J Am Soc Nephrol: JASN 22:1551–1559
Finn JE, Mathieson PW (1993) Molecular analysis of C3 allotypes in patients with nephritic factor. Clin Exp Immunol 91:410–414
Daha MR, Fearon DT, Austen KF (1976) C3 nephritic factor (C3NeF): stabilization of fluid phase and cell-bound alternative pathway convertase. J Immunol 116:1–7
Daha MR, Austen KF, Fearon DT (1977) The incorporation of C3 nephritic factor (C3NeF) into a stabilized C3 convertase, C3bBb (C3NeF), and its release after decay of convertase function. J Immunol 119:812–817
Sissons JG, West RJ, Fallows J, Williams DG, Boucher BJ, Amos N et al (1976) The complement abnormalities of lipodystrophy. N Engl J Med 294:461–465
Gewurz AT, Imherr SM, Strauss S, Gewurz H, Mold C (1983) C3 nephritic factor and hypocomplementaemia in a clinically healthy individual. Clin Exp Immunol 54:253–258
Strobel S, Zimmering M, Papp K, Prechl J, Jozsi M (2010) Anti-factor B autoantibody in dense deposit disease. Mol Immunol 47:1476–1483
Chen Q, Muller D, Rudolph B, Hartmann A, Kuwertz-Broking E, Wu K et al (2011) Combined C3b and factor B autoantibodies and MPGN type II. N Engl J Med 365:2340–2342
Goodship TH, Pappworth IY, Toth T, Denton M, Houlberg K, McCormick F et al (2012) Factor H autoantibodies in membranoproliferative glomerulonephritis. Mol Immunol 52:200–206
Blanc C, Togarsimalemath SK, Chauvet S, Le Quintrec M, Moulin B, Buchler M et al (2015) Anti-factor H autoantibodies in C3 glomerulopathies and in atypical hemolytic uremic syndrome: one target, two diseases. J Immunol 194:5129–5138
Meri S, Koistinen V, Miettinen A, Tornroth T, Seppala IJ (1992) Activation of the alternative pathway of complement by monoclonal lambda light chains in membranoproliferative glomerulonephritis. J Exp Med 175:939–950
Zand L, Kattah A, Fervenza FC, Smith RJ, Nasr SH, Zhang Y et al (2013) C3 glomerulonephritis associated with monoclonal gammopathy: a case series. Am J Kidney Dis: Off J Natl Kidney Found 62:506–514
Cansick JC, Lennon R, Cummins CL, Howie AJ, McGraw ME, Saleem MA et al (2004) Prognosis, treatment and outcome of childhood mesangiocapillary (membranoproliferative) glomerulonephritis. Nephrol Dial Transplant 19:2769–2777
Braun MC, Stablein DM, Hamiwka LA, Bell L, Bartosh SM, Strife CF (2005) Recurrence of membranoproliferative glomerulonephritis type II in renal allografts: the North American Pediatric Renal Transplant Cooperative Study experience. J Am Soc Nephrol: JASN 16:2225–2233
Varade WS, Forristal J, West CD (1990) Patterns of complement activation in idiopathic membranoproliferative glomerulonephritis, types I, II, and III. Am J Kidney Dis: Off J Natl Kidney Found 16:196–206
Eisinger AJ, Shortland JR, Moorhead PJ (1972) Renal disease in partial lipodystrophy. Q J Med 41:343–354
Misra A, Peethambaram A, Garg A (2004) Clinical features and metabolic and autoimmune derangements in acquired partial lipodystrophy: report of 35 cases and review of the literature. Medicine 83:18–34
Hageman GS, Mullins RF, Russell SR, Johnson LV, Anderson DH (1999) Vitronectin is a constituent of ocular drusen and the vitronectin gene is expressed in human retinal pigmented epithelial cells. FASEB J 13:477–484
Tarshish P, Bernstein J, Tobin JN, Edelmann CM Jr (1992) Treatment of mesangiocapillary glomerulonephritis with alternate-day prednisone—a report of the International Study of Kidney Disease in Children. Pediatr Nephrol 6:123–130
Faedda R, Satta A, Tanda F, Pirisi M, Bartoli E (1994) Immunosuppressive treatment of membranoproliferative glomerulonephritis. Nephron 67:59–65
Jones G, Juszczak M, Kingdon E, Harber M, Sweny P, Burns A (2004) Treatment of idiopathic membranoproliferative glomerulonephritis with mycophenolate mofetil and steroids. Nephrol Dial Transplant 19:3160–3164
Rabasco C, Cavero T, Roman E, Rojas-Rivera J, Olea T, Espinosa M et al (2015) Effectiveness of mycophenolate mofetil in C3 glomerulonephritis. Kidney Int 88:1153–1160
Zauner I, Bohler J, Braun N, Grupp C, Heering P, Schollmeyer P (1994) Effect of aspirin and dipyridamole on proteinuria in idiopathic membranoproliferative glomerulonephritis: a multicentre prospective clinical trial. Collaborative Glomerulonephritis Therapy Study Group (CGTS). Nephrol Dial Transplant 9:619–622
Donadio JV Jr, Anderson CF, Mitchell JC 3rd, Holley KE, Ilstrup DM, Fuster V et al (1984) Membranoproliferative glomerulonephritis. A prospective clinical trial of platelet-inhibitor therapy. N Engl J Med 310:1421–1426
Donadio JV Jr, Offord KP (1989) Reassessment of treatment results in membranoproliferative glomerulonephritis, with emphasis on life-table analysis. Am J Kidney Dis: Official J Natl Kidney Found 14:445–451
Farooqui M, Alsaad K, Aloudah N, Alhamdan H (2015) Treatment-resistant recurrent membranoproliferative glomerulonephritis in renal allograft responding to rituximab: case report. Transplant Proc 47:823–826
Marques ID, Ramalho J, David DR, Nahas WC, David-Neto E (2014) Rituximab in a B cell-driven regimen for the treatment of recurrent membranoproliferative glomerulonephritis after kidney transplantation. Int Urol Nephrol 46:2053–2054
Giaime P, Daniel L, Burtey S (2015) Remission of C3 glomerulopathy with rituximab as only immunosuppressive therapy. Clin Nephrol 83:57–60
(2016) (Eculizumab in primary MPGN—full text view - ClinicalTrials.gov
Bomback AS, Smith RJ, Barile GR, Zhang Y, Heher EC, Herlitz L et al (2012) Eculizumab for dense deposit disease and C3 glomerulonephritis. Clin J Am Soc Nephrol: CJASN 7:748–756
McCaughan JA, O’Rourke DM, Courtney AE (2012) Recurrent dense deposit disease after renal transplantation: an emerging role for complementary therapies. Am J Transplant Off J Am Soc Transplant Am Soc Transplant Surg 12:1046–1051
Rousset-Rouviere C, Cailliez M, Garaix F, Bruno D, Laurent D, Tsimaratos M (2014) Rituximab fails where eculizumab restores renal function in C3nef-related DDD. Pediatr Nephrol 29:1107–1111
Le Quintrec M, Lionet A, Kandel C, Bourdon F, Gnemmi V, Colombat M et al (2015) Eculizumab for treatment of rapidly progressive C3 glomerulopathy. Am J Kidney Dis: Off J Natl Kidney Found 65:484–489
Inman M, Prater G, Fatima H, Wallace E (2015) Eculizumab-induced reversal of dialysis-dependent kidney failure from C3 glomerulonephritis. Clin Kidney J 8:445–448
Habbig S, Mihatsch MJ, Heinen S, Beck B, Emmel M, Skerka C et al (2009) C3 deposition glomerulopathy due to a functional factor H defect. Kidney Int 75:1230–1234
Zhang Y, Nester CM, Holanda DG, Marsh HC, Hammond RA, Thomas LJ et al (2013) Soluble CR1 therapy improves complement regulation in C3 glomerulopathy. J Am Soc Nephrol: JASN 24:1820–1829
Strubing P (1882) Paroxysmale haemoglobinurie. Dtsch Med Wochenschr 8:1–16
Hill A, DeZern AE, Kinoshita T, Brodsky RA (2017) Paroxysmal nocturnal haemoglobinuria. Nat Rev Dis Primers 3:17028
Socie G, Schrezenmeier H, Muus P, Lisukov I, Roth A, Kulasekararaj A et al (2016) Changing prognosis in paroxysmal nocturnal haemoglobinuria disease subcategories: an analysis of the International PNH Registry. Intern Med J 46:1044–1053
Ware RE, Hall SE, Rosse WF (1991) Paroxysmal nocturnal hemoglobinuria with onset in childhood and adolescence. N Engl J Med 325:991–996
Takeda J, Miyata T, Kawagoe K, Iida Y, Endo Y, Fujita T et al (1993) Deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria. Cell 73:703–711
Oni SB, Osunkoya BO, Luzzatto L (1970) Paroxysmal nocturnal hemoglobinuria: evidence for monoclonal origin of abnormal red cells. Blood 36:145–152
Kinoshita T, Medof ME, Silber R, Nussenzweig V (1985) Distribution of decay-accelerating factor in the peripheral blood of normal individuals and patients with paroxysmal nocturnal hemoglobinuria. J Exp Med 162:75–92
Nafa K, Bessler M, Castro-Malaspina H, Jhanwar S, Luzzatto L (1998) The spectrum of somatic mutations in the PIG-A gene in paroxysmal nocturnal hemoglobinuria includes large deletions and small duplications. Blood Cells Mol Dis 24:370–384
Nafa K, Mason PJ, Hillmen P, Luzzatto L, Bessler M (1995) Mutations in the PIG-A gene causing paroxysmal nocturnal hemoglobinuria are mainly of the frameshift type. Blood 86:4650–4655
Luzzatto L (1999) Paroxysmal murine hemoglobinuria(?): a model for human PNH. Blood 94:2941–2944
Rosti V (2002) Murine models of paroxysmal nocturnal hemoglobinuria. Ann N Y Acad Sci 963:290–296
Inoue N, Izui-Sarumaru T, Murakami Y, Endo Y, Nishimura J, Kurokawa K et al (2006) Molecular basis of clonal expansion of hematopoiesis in 2 patients with paroxysmal nocturnal hemoglobinuria (PNH). Blood 108:4232–4236
Rotoli B, Luzzatto L (1989) Paroxysmal nocturnal hemoglobinuria. Semin Hematol 26:201–207
Ohishi K, Inoue N, Kinoshita T (2001) PIG-S and PIG-T, essential for GPI anchor attachment to proteins, form a complex with GAA1 and GPI8. EMBO J 20:4088–4098
Krawitz PM, Hochsmann B, Murakami Y, Teubner B, Kruger U, Klopocki E et al (2013) A case of paroxysmal nocturnal hemoglobinuria caused by a germline mutation and a somatic mutation in PIGT. Blood 122:1312–1315
Kinoshita T, Fujita M (2016) Biosynthesis of GPI-anchored proteins: special emphasis on GPI lipid remodeling. J Lipid Res 57:6–24
Hill A, Kelly RJ, Hillmen P (2013) Thrombosis in paroxysmal nocturnal hemoglobinuria. Blood 121:4985–4996
Wong EK, Kavanagh D (2015) Anticomplement C5 therapy with eculizumab for the treatment of paroxysmal nocturnal hemoglobinuria and atypical hemolytic uremic syndrome. Transl Res 165:306–320
Rother RP, Bell L, Hillmen P, Gladwin MT (2005) The clinical sequelae of intravascular hemolysis and extracellular plasma hemoglobin: a novel mechanism of human disease. JAMA 293:1653–1662
Clark DA, Butler SA, Braren V, Hartmann RC, Jenkins DE Jr (1981) The kidneys in paroxysmal nocturnal hemoglobinuria. Blood 57:83–89
Nath KA, Vercellotti GM, Grande JP, Miyoshi H, Paya CV, Manivel JC et al (2001) Heme protein-induced chronic renal inflammation: suppressive effect of induced heme oxygenase-1. Kidney Int 59:106–117
de Latour RP, Mary JY, Salanoubat C, Terriou L, Etienne G, Mohty M et al (2008) Paroxysmal nocturnal hemoglobinuria: natural history of disease subcategories. Blood 112:3099–3106
Socie G, Mary JY, de Gramont A, Rio B, Leporrier M, Rose C et al (1996) Paroxysmal nocturnal haemoglobinuria: long-term follow-up and prognostic factors. French Society of Haematology. Lancet 348:573–577
Hillmen P, Lewis SM, Bessler M, Luzzatto L, Dacie JV (1995) Natural history of paroxysmal nocturnal hemoglobinuria. N Engl J Med 333:1253–1258
Kelly RJ, Hill A, Arnold LM, Brooksbank GL, Richards SJ, Cullen M et al (2011) Long-term treatment with eculizumab in paroxysmal nocturnal hemoglobinuria: sustained efficacy and improved survival. Blood 117:6786–6792
Hillmen P, Young NS, Schubert J, Brodsky RA, Socie G, Muus P et al (2006) The complement inhibitor eculizumab in paroxysmal nocturnal hemoglobinuria. N Engl J Med 355:1233–1243
Hill A, Hillmen P, Richards SJ, Elebute D, Marsh JC, Chan J et al (2005) Sustained response and long-term safety of eculizumab in paroxysmal nocturnal hemoglobinuria. Blood 106:2559–2565
Hillmen P, Muus P, Duhrsen U, Risitano AM, Schubert J, Luzzatto L et al (2007) Effect of the complement inhibitor eculizumab on thromboembolism in patients with paroxysmal nocturnal hemoglobinuria. Blood 110:4123–4128
Hillmen P, Elebute M, Kelly R, Urbano-Ispizua A, Hill A, Rother RP et al (2010) Long-term effect of the complement inhibitor eculizumab on kidney function in patients with paroxysmal nocturnal hemoglobinuria. Am J Hematol 85:553–559
Risitano AM, Notaro R, Marando L, Serio B, Ranaldi D, Seneca E et al (2009) Complement fraction 3 binding on erythrocytes as additional mechanism of disease in paroxysmal nocturnal hemoglobinuria patients treated by eculizumab. Blood 113:4094–4100
Rondelli T, Risitano AM, Peffault de Latour R, Sica M, Peruzzi B, Ricci P et al (2014) Polymorphism of the complement receptor 1 gene correlates with the hematologic response to eculizumab in patients with paroxysmal nocturnal hemoglobinuria. Haematologica 99:262–266
Harris CL (2017) Expanding horizons in complement drug discovery: challenges and emerging strategies. Semin Immunopathol. https://doi.org/10.1007/s00281-017-0655-8
This article is a contribution to the special issue on Complement in Health and Disease: Novel Aspects and Insights - Guest Editors: Paul Morgan and David Kavanagh
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Wong, E.K.S., Kavanagh, D. Diseases of complement dysregulation—an overview. Semin Immunopathol 40, 49–64 (2018). https://doi.org/10.1007/s00281-017-0663-8
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