Skip to main content

Advertisement

Log in

Gastrointestinal Disorders Associated with Primary Immunodeficiency Diseases

  • Published:
Clinical Reviews in Allergy & Immunology Aims and scope Submit manuscript

Abstract

There are now 354 inborn errors of immunity (primary immunodeficiency diseases (PIDDs)) with 344 distinct molecular etiologies reported according to the International Union of Immunological Sciences (IUIS) (Clin Gastroenterol Hepatol 11: p. 1050-63, 2013, Semin Gastrointest Dis 8: p. 22-32, 1997, J Clin Immunol 38: p. 96-128, 2018). Using the IUIS document as a reference and cross-checking PubMed (www.ncbi.nlm.nih.pubmed.gov), we found that approximately one third of the 354 diseases of impaired immunity have a gastrointestinal component [J Clin Immunol 38: p. 96-128, 2018]. Often, the gastrointestinal symptomatology and pathology is the heralding sign of a PIDD; therefore, it is important to recognize patterns of disease which may manifest along the gastrointestinal tract as a more global derangement of immune function. As such, holistic consideration of immunity is warranted in patients with clinically significant gastrointestinal disease. Here, we discuss the manifold presentations and GI-specific complications of PIDDs which could lead patients to seek advice from a variety of clinician specialists. Often, patients with these medical problems will engage general pediatricians, surgeons, gastroenterologists, rheumatologists, and clinical immunologists among others. Following delineation of the presenting concern, accurate and often molecular diagnosis is imperative and a multi-disciplinary approach warranted for optimal management. In this review, we will summarize the current state of understanding of PIDD gastrointestinal disease involvement. We will do so by focusing upon gastrointestinal disease categories (i.e., inflammatory, diarrhea, nodular lymphoid hyperplasia, liver/biliary tract, structural disease, and oncologic disease) with an intent to aid the healthcare provider who may encounter a patient with an as-yet undiagnosed PIDD who presents initially with a gastrointestinal symptom, sign, or problem.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1

Similar content being viewed by others

References

  1. Petersen BS, August D, Abt R, Alddafari M, Atarod L, Baris S, Bhavsar H, Brinkert F, Buchta M, Bulashevska A, Chee R, Cordeiro AI, Dara N, Dückers G, Elmarsafy A, Frede N, Galal N, Gerner P, Glocker EO, Goldacker S, Hammermann J, Hasselblatt P, Havlicekova Z, Hübscher K, Jesenak M, Karaca NE, Karakoc-Aydiner E, Kharaghani MM, Kilic SS, Kiykim A, Klein C, Klemann C, Kobbe R, Kotlarz D, Laass MW, Leahy TR, Mesdaghi M, Mitton S, Neves JF, Öztürk B, Pereira LF, Rohr J, Restrepo JLR, Ruzaike G, Saleh N, Seneviratne S, Senol E, Speckmann C, Tegtmeyer D, Thankam P, van der Werff ten Bosch J, von Bernuth H, Zeissig S, Zeissig Y, Franke A, Grimbacher B (2017) Targeted gene panel sequencing for early-onset inflammatory bowel disease and chronic diarrhea. Inflamm Bowel Dis 23(12):2109–2120

    Article  PubMed  Google Scholar 

  2. Glocker EO, Kotlarz D, Boztug K, Gertz EM, Schäffer AA, Noyan F, Perro M, Diestelhorst J, Allroth A, Murugan D, Hätscher N, Pfeifer D, Sykora KW, Sauer M, Kreipe H, Lacher M, Nustede R, Woellner C, Baumann U, Salzer U, Koletzko S, Shah N, Segal AW, Sauerbrey A, Buderus S, Snapper SB, Grimbacher B, Klein C (2009) Inflammatory bowel disease and mutations affecting the interleukin-10 receptor. N Engl J Med 361(21):2033–2045

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  3. Atarod L et al (2003) A review of gastrointestinal disorders in patients with primary antibody immunodeficiencies during a 10-year period (1990–2000), in children hospital medical center. Iran J Allergy Asthma Immunol 2(2):75–79

    PubMed  Google Scholar 

  4. Glocker E, Grimbacher B (2012) Inflammatory bowel disease: is it a primary immunodeficiency? Cell Mol Life Sci 69(1):41–48

    Article  CAS  PubMed  Google Scholar 

  5. Henderson P, Hansen R, Cameron FL, Gerasimidis K, Rogers P, Bisset MW, Reynish EL, Drummond HE, Anderson NH, van Limbergen J, Russell RK, Satsangi J, Wilson DC (2012) Rising incidence of pediatric inflammatory bowel disease in Scotland. Inflamm Bowel Dis 18:999–1005

    Article  PubMed  Google Scholar 

  6. Benchimol E et al (2014) Incidence, outcomes and health services burden of children with very early onset inflammatory bowel disease. Gastroenterology 147:803–813.e7

    Article  PubMed  Google Scholar 

  7. Silverberg M et al (2005) Toward an integrated clinical, molecular and serological classification of inflammatory bowel disease: report of a Working Party of the 2005 Montreal World Congress of Gastroenterology. Can J Gastroenterol 19(suppl A):5A–36A

    Article  PubMed  Google Scholar 

  8. Uhlig HH et al (2014) The Diagnostic Approach to Monogenic Very Early Onset Inflammatory Bowel Disease. Gastroenterology 147:990–1007

    Article  PubMed  Google Scholar 

  9. Levine A, Griffiths A, Markowitz J, Wilson DC, Turner D, Russell RK, Fell J, Ruemmele FM, Walters T, Sherlock M, Dubinsky M, Hyams JS (2011) Pediatric modification of the Montreal classification for inflammatory bowel disease: the Paris classification. Inflamm Bowel Dis 17:1314–1321

    Article  PubMed  Google Scholar 

  10. Agarwal S, Mayer L (2013) Diagnosis and treatment of gastrointestinal disorders in patients with primary immunodeficiency. Clin Gastroenterol Hepatol 11(9):1050–1063

    Article  PubMed  PubMed Central  Google Scholar 

  11. Ament ME (1985) Immunodeficiency syndromes and the gut. Scand J Gastroenterol Suppl 114:127–135

    Article  CAS  PubMed  Google Scholar 

  12. Mulholland MW et al (1983) Gastrointestinal complications of congenital immunodeficiency states. The surgeon’s role. Ann Surg 198(6):673–680

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  13. Bonilla FA, Barlan I, Chapel H, Costa-Carvalho BT, Cunningham-Rundles C, de la Morena MT, Espinosa-Rosales FJ, Hammarström L, Nonoyama S, Quinti I, Routes JM, Tang MLK, Warnatz K (2016) International consensus document (ICON): common variable immunodeficiency disorders. J Allergy Clin Immunol 4(1):38–59

    Article  Google Scholar 

  14. Pecoraro A, Nappi L, Crescenzi L, D’Armiento FP, Genovese A, Spadaro G (2018) Chronic diarrhea in common variable immunodeficiency: a case series and review of the literature. J Clin Immunol 38:67–76

    Article  PubMed  Google Scholar 

  15. Picard C, Bobby Gaspar H, al-Herz W, Bousfiha A, Casanova JL, Chatila T, Crow YJ, Cunningham-Rundles C, Etzioni A, Franco JL, Holland SM, Klein C, Morio T, Ochs HD, Oksenhendler E, Puck J, Tang MLK, Tangye SG, Torgerson TR, Sullivan KE (2018) International Union of Immunological Societies: 2017 Primary Immunodeficiency Diseases Committee report on inborn errors of immunity. J Clin Immunol 38(1):96–128

    Article  PubMed  Google Scholar 

  16. Kammermeier J, Dziubak R, Pescarin M, Drury S, Godwin H, Reeve K, Chadokufa S, Huggett B, Sider S, James C, Acton N, Cernat E, Gasparetto M, Noble-Jamieson G, Kiparissi F, Elawad M, Beales PL, Sebire NJ, Gilmour K, Uhlig HH, Bacchelli C, Shah N (2017) Phenotypic and genotypic characterisation of inflammatory bowel disease presenting before the age of 2 years. J Crohn’s Colitis 11:60–69

    Article  Google Scholar 

  17. Quigley E, Carmichael H, Watkinson G (1986) Case report and review of the relationships between vitamin B12 deficiency, small intestinal mucosal disease and immunoglobulin deficiency. J Clin Gastroenterol 8:277–281

    Article  CAS  PubMed  Google Scholar 

  18. Spector J (1974) Juvenile achlorhydric pernicious anemia with IgA deficiency. A family study. JAMA 228:334–336

    Article  CAS  PubMed  Google Scholar 

  19. Barzaghi F, Passerini L, Bacchetta R (2012) Immune dysregulation, polyendocrinopathy, enteropathy, x-linked syndrome: a paradigm of immunodeficiency with autoimmunity. Front Immunol 3:211

    Article  PubMed  PubMed Central  Google Scholar 

  20. Bennett CL, Christie J, Ramsdell F, Brunkow ME, Ferguson PJ, Whitesell L, Kelly TE, Saulsbury FT, Chance PF, Ochs HD (2001) The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3. Nat Genet 27(1):20–21

    Article  CAS  PubMed  Google Scholar 

  21. Gambineri E et al (2008) Clinical and molecular profile of a new series of patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome: inconsistent correlation between forkhead box protein 3 expression and disease severity. J Allergy Clin Immunol 122(6):1105–1112 e1

    Article  CAS  PubMed  Google Scholar 

  22. Duclaux-Loras R, Collardeau-Frachon S, Nancey S, Fabien N, Kaiserlian D, Lachaux A (2015) Long-term disease course in a patient with severe neonatal IPEX syndrome. Clin Res Hepatol Gastroenterol 39(4):e43–e47

    Article  PubMed  Google Scholar 

  23. Guerrerio AL, Frischmeyer-Guerrerio PA, Lederman HM, Oliva-Hemker M (2010) Recognizing gastrointestinal and hepatic manifestations of primary immunodeficiency diseases. J Pediatr Gastroenterol Nutr 51(5):548–555

    Article  PubMed  Google Scholar 

  24. Scaillon M, van Biervliet S, Bontems P, Dorchy H, Hanssens L, Ferster A, Segers V, Cadranel S (2009) Severe gastritis in an insulin-dependent child with an IPEX syndrome. J Pediatr Gastroenterol Nutr 49(3):368–370

    Article  CAS  PubMed  Google Scholar 

  25. D’Hennezel E et al (2009) FOXP3 forkhead domain mutation and regulatory T cells in the IPEX sydrome. NEJM 17(Oct 22 361):1710–1713

    Article  Google Scholar 

  26. de Serre Patey-Mariaud N et al (2009) Digestive histopathological presentation of IPEX syndrome. Mod Pathol 22(1):95–102

    Article  CAS  Google Scholar 

  27. Torgerson TR, Linane A, Moes N, Anover S, Mateo V, Rieux–Laucat F, Hermine O, Vijay S, Gambineri E, Cerf–Bensussan N, Fischer A, Ochs HD, Goulet O, Ruemmele FM (2007) Severe food allergy as a variant of IPEX syndrome caused by a deletion in a noncoding region of the FOXP3 gene. Gastroenterology 132(5):1705–1717

    Article  CAS  PubMed  Google Scholar 

  28. Barzaghi F et al (2017) Long-term follow up of IPEX syndrome patients after different therapeutic strategies: an international multicenter retrospective study. J Allergy Clin Immunol 17(Epub ahead of print):31893–31896

    Google Scholar 

  29. Caudy AA, Reddy ST, Chatila T, Atkinson JP, Verbsky JW (2007) CD25 deficiency causes an immune dysregulation, polyendocrinopathy, enteropathy, X-linked-like syndrome, and defective IL-10 expression from CD4 lymphocytes. J Allergy Clin Immunol 119(2):482–487

    Article  CAS  PubMed  Google Scholar 

  30. Kwan A et al (2014) Newborn screening for severe combined immunodeficiency in 11 screening programs in the United States. JAMA 312(7):729–738

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  31. Ozgur T et al (2008) Hematopoietic stem cell transplantation in a CD3 gamma-deficient infant with inflammatory bowel disease. Pediatr Transplant 12(8):910–913

    Article  PubMed  Google Scholar 

  32. Alroqui F et al (2017) DOCK8 deficiency presenting as an IPEX-like disorder. J Clin Immunol 37(8):811–819

    Article  CAS  Google Scholar 

  33. Stray-Pedersen A, Sorte HS, Samarakoon P, Gambin T, Chinn IK, Coban Akdemir ZH, Erichsen HC, Forbes LR, Gu S, Yuan B, Jhangiani SN, Muzny DM, Rødningen OK, Sheng Y, Nicholas SK, Noroski LM, Seeborg FO, Davis CM, Canter DL, Mace EM, Vece TJ, Allen CE, Abhyankar HA, Boone PM, Beck CR, Wiszniewski W, Fevang B, Aukrust P, Tjønnfjord GE, Gedde-Dahl T, Hjorth-Hansen H, Dybedal I, Nordøy I, Jørgensen SF, Abrahamsen TG, Øverland T, Bechensteen AG, Skogen V, Osnes LTN, Kulseth MA, Prescott TE, Rustad CF, Heimdal KR, Belmont JW, Rider NL, Chinen J, Cao TN, Smith EA, Caldirola MS, Bezrodnik L, Lugo Reyes SO, Espinosa Rosales FJ, Guerrero-Cursaru ND, Pedroza LA, Poli CM, Franco JL, Trujillo Vargas CM, Aldave Becerra JC, Wright N, Issekutz TB, Issekutz AC, Abbott J, Caldwell JW, Bayer DK, Chan AY, Aiuti A, Cancrini C, Holmberg E, West C, Burstedt M, Karaca E, Yesil G, Artac H, Bayram Y, Atik MM, Eldomery MK, Ehlayel MS, Jolles S, Flatø B, Bertuch AA, Hanson IC, Zhang VW, Wong LJ, Hu J, Walkiewicz M, Yang Y, Eng CM, Boerwinkle E, Gibbs RA, Shearer WT, Lyle R, Orange JS, Lupski JR (2017) Primary immunodeficiency diseases: genomic approaches delineate heterogeneous Mendelian disorders. J Allergy Clin Immunol 139(1):232–245

    Article  PubMed  Google Scholar 

  34. Vlantis K et al (2016) NEMO prevents RIP kinase 1-mediated epithelial cell death and chronic intestinal inflammation by NK-kB-dependent and -independent functions. Immunity 33(3):553–567

    Article  CAS  Google Scholar 

  35. Nenci A et al (2007) Epithelial NEMO links innate immunity to chronic intestinal inflammation. Nature 446(7135):557–561

    Article  CAS  PubMed  Google Scholar 

  36. Tegtmeyer D et al (2017) Inflammatory bowel disease caused by primary immunodeficiencies—clinical presentations, review of literature and proposal of a rational diagnostic algorithm. Pediatr Allergy Immunol 28(5):412–429

    Article  PubMed  Google Scholar 

  37. Klemann C, Pannicke U, Morris-Rosendahl DJ, Vlantis K, Rizzi M, Uhlig H, Vraetz T, Speckmann C, Strahm B, Pasparakis M, Schwarz K, Ehl S, Rohr JC (2016) Transplantation from a symptomatic carrier sister restores host defenses but does not prevent colitis in NEMO deficiency. Clin Immunol 164(Mar):52–56

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  38. Permaul P, Narla A, Hornick JL, Pai SY (2009) Allogeneic hematopoietic stem cell transplantation for X-linked ectodermal dysplasia and immunodeficiency: case report and review of outcomes. Immunol Res 44(1–3):89–98

    Article  PubMed  Google Scholar 

  39. Cheng LE, Kanwar B, Tcheurekdjian H, Grenert JP, Muskat M, Heyman MB, McCune JM, Wara DW (2009) Persistent systemic inflammation and atypical enterocolitis in patients with NEMO syndrome. Clin Immunol 132(1):124–131

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  40. Mizukami T, Obara M, Nishikomori R, Kawai T, Tahara Y, Sameshima N, Marutsuka K, Nakase H, Kimura N, Heike T, Nunoi H (2012) Successful treatment with infliximab for inflammatory colitis in a patient with X-linked anhidrotic ectodermal dysplasia with immunodeficiency. J Clin Immunol 32(1):39–49

    Article  PubMed  Google Scholar 

  41. Barmettler S, Otani IM, Minhas J, Abraham RS, Chang Y, Dorsey MJ, Ballas ZK, Bonilla FA, Ochs HD, Walter JE (2017) Gastrointestinal manifestations in X-linked agammaglobulinemia. J Clin Immunol 37(3):287–294

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  42. Washington K, Stenzel TT, Buckley RH, Gottfried MR (1996) Gastrointestinal pathology in patients with common variable immunodeficiency and X-linked agammaglobulinemia. Am J Surg Pathol 20(10):1240–1252

    Article  CAS  PubMed  Google Scholar 

  43. Shera IA, Khurshid SM, Bhat MS (2017) Inflammatory duodenal polyposis associated with primary immunodeficiency disease: a novel case report. Case Rep Med 2017:6206085

    Article  PubMed  PubMed Central  Google Scholar 

  44. Hernandez-Trujillo V et al (2014) Autoimmunity and inflammation in X-linked agammaglobulinemia. J Clin Immunol 34(6):627–632

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  45. Kalha I, Sellin JH (2004) Common variable immunodeficiency and the gastrointestinal tract. Curr Gastroenterol Rep 6(5):377–383

    Article  PubMed  Google Scholar 

  46. Al-Muhsen S (2010) Gastrointestinal and hepatic manifestations of primary immunodeficiency diseases. Saudi J Gastroenterol 16(2):66–74

    Article  PubMed  PubMed Central  Google Scholar 

  47. Cunningham-Rundles C, Bodian C (1999) Common variable immunodeficiency: clinical and immunological features of 248 patients. Clin Immunol 92(1):34–48

    Article  CAS  PubMed  Google Scholar 

  48. Hermaszewski R, Webster A (1993) Primary hypogammaglobulinemia: a survey of clinical manifestations and complications. Q J Med 86(1):31–42

    CAS  PubMed  Google Scholar 

  49. Oksenhendler E et al (2008) Infections in 252 patients with common variable immunodeficiency. Clin Infect Dis 46(10):1547–1554

    Article  PubMed  Google Scholar 

  50. Wood P, Stanworth S, Burton J, Jones A, Peckham DG, Green T, Hyde C, Chapel H, the UK Primary Immunodeficiency Network (2007) Recognition, clinical diagnosis and management of patients with primary antibody deficiencies: a systematic review. Clin Exp Immunol 149(3):410–423

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  51. Khodadad A, Aghamohammadi A, Parvaneh N, Rezaei N, Mahjoob F, Bashashati M, Movahedi M, Fazlollahi MR, Zandieh F, Roohi Z, Abdollahzade S, Salavati A, Kouhi A, Talebpour B, Daryani NE (2007) Gastrointestinal manifestations in patients with common variable immunodeficiency. Dig Dis Sci 52(11):2977–2983

    Article  PubMed  Google Scholar 

  52. Mannon PJ, Fuss IJ, Dill S, Friend J, Groden C, Hornung R, Yang Z, Yi C, Quezado M, Brown M, Strober W (2006) Excess IL-12 but not IL-23 accompanies the inflammatory bowel disease associated with common variable immunodeficiency. Gastroenterology 131(3):748–756

    Article  CAS  PubMed  Google Scholar 

  53. Luzi G, Zullo A, Iebba F, Rinaldi V, Mete LS, Muscaritoli M, Aiuti F (2003) Duodenal pathology and clinical-immunological implications in common variable immunodeficiency patients. Am J Gastroenterol 98(1):118–121

    Article  PubMed  Google Scholar 

  54. Daniels JA, Lederman HM, Maitra A, Montgomery EA (2007) Gastrointestinal tract pathology in patients with common variable immunodeficiency (CVID): a clinicopathologic study and review. Am J Surg Pathol 31(12):1800–1812

    Article  PubMed  Google Scholar 

  55. Hermans PE, Diaz-Buxo JA, Stobo JD (1976) Idiopathic late-onset immunoglobulin deficiency. Clinical observations in 50 patients. Am J Med 61(2):221–237

    Article  CAS  PubMed  Google Scholar 

  56. Twomey JJ, Jordan PH, Jarrold T, Trubowitz S, Ritz ND, Conn HO (1969) The syndrome of immunoglobulin deficiency and pernicious anemia. A study of ten cases. Am J Med 47(3):340–350

    Article  CAS  PubMed  Google Scholar 

  57. Quinti I et al (2007) Long-term follow up and outcome of a large cohort of patients with common variable immunodeficiency. J Clin Immunol 27(3):308–316

    Article  PubMed  Google Scholar 

  58. Agarwal S, Smereka P, Harpaz N, Cunningham-Rundles C, Mayer L (2011) Characterization of immunologic defects in patients with common variable immunodeficiency (CVID) with intestinal disease. Inflamm Bowel Dis 17(1):251–259

    Article  PubMed  Google Scholar 

  59. Dhalla F, da Silva SP, Lucas M, Travis S, Chapel H (2011) Review of gastric cancer risk factors in patients with common variable immunodeficiency disorders, resulting in a proposal for a surveillance programme. Clin Exp Immunol 165(1):1–7

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  60. Comunoglu, N., S.Kara, and N.Kepil, (2015) Inflammatory bowel disease-like colitis pathology in a patient with common variable immune deficiency. BMJ Case Rep 2015

  61. Bosworth BP, Sanders A, Maltz C (2006) Common variable immunodeficiency masquerading as Crohn’s ileocolitis. Inflamm Bowel Dis 12(2):151–152

    Article  PubMed  Google Scholar 

  62. Mudter J, Wirtz S, Weigmann B, Tiede I, Tubbe I, Kiesslich R, Galle PR, Lehr HA, Neurath MF (2006) Crohn’s-like colitis in a patient with immunodeficiency associated with a defect in expression of inducible costimulator. Dig Dis Sci 51(4):711–717

    Article  PubMed  Google Scholar 

  63. Baehner RL, Karnovsky ML (1968. Dec 13) Deficiency of reduced nicotinamide-adenine dinucleotide oxidase in chronic granulomatous disease. Science 162(3859):1277–1279

    Article  CAS  PubMed  Google Scholar 

  64. McPhail LC et al (1977) Deficiency of NADPH oxidase activity in chronic granulomatous disease. J Pediatr 90(2):213–217

    Article  CAS  PubMed  Google Scholar 

  65. Abo A et al (1994) Activation of NADPH oxidase involves the dissociation of p21rac from its inhibitory GDP/GTP exchange protein (rhoGDI) followed by its translocation to the plasma membrane. Biochem J 298(Pt3):585–591

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  66. Hampton MB, Kettle AJ, Winterbourn CC (1996) Involvement of superoxide and myeloperoxidase in oxygen-dependent killing of Staphylococcus aureus by neutrophils. Infect Immun 64(9):3512–3517

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  67. Rosen H, Klebanoff SJ (1979) Bactericidal activity of a superoxide anion-generating system. A model for the polymorphonuclear leukocyte. J Exp Med 149(1):27–39

    Article  CAS  PubMed  Google Scholar 

  68. Kaplan EL, Laxdal T, Quie PG (1968) Studies of polymorphonuclear leukocytes from patients with chronic granulomatous disease of childhood; bactericidal capacity for streptococci. Pediatrics 41(3):591–599

    Article  CAS  PubMed  Google Scholar 

  69. Magnani A et al (2014) Inflammatory manifestations in a single-center cohort of patients with chronic granulomatous disease. J Allergy Clin Immunol 134(3):655–662 e8

    Article  PubMed  Google Scholar 

  70. van den Berg JM, van Koppen E, Åhlin A, Belohradsky BH, Bernatowska E, Corbeel L, Español T, Fischer A, Kurenko-Deptuch M, Mouy R, Petropoulou T, Roesler J, Seger R, Stasia MJ, Valerius NH, Weening RS, Wolach B, Roos D, Kuijpers TW (2009) Chronic granulomatous disease: the European experience. PLoS One 4(4):e5234

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  71. Raptaki M, Varela I, Spanou K, Tzanoudaki M, Tantou S, Liatsis M, Constantinidou N, Bakoula C, Roos D, Kanariou M (2013) Chronic granulomatous disease: a 25-year patient registry based on a multistep diagnostic procedure, from the referral center for primary immunodeficiencies in Greece. J Clin Immunol 33(8):1302–1309

    Article  PubMed  Google Scholar 

  72. Marciano BE, Rosenzweig SD, Kleiner DE, Anderson VL, Darnell DN, Anaya-O'Brien S, Hilligoss DM, Malech HL, Gallin JI, Holland SM (2004) Gastrointestinal involvement in chronic granulomatous disease. Pediatrics 114(2):462–468

    Article  PubMed  Google Scholar 

  73. Winkelstein JA, Marino MC, Johnston RB Jr, Boyle J, Curnutte J, Gallin JI, Malech HL, Holland SM, Ochs H, Quie P, Buckley RH, Foster CB, Chanock SJ, Dickler H (2000) Chronic granulomatous disease. Report on a national registry of 368 patients. Medicine (Baltimore) 79(3):155–169

    Article  CAS  Google Scholar 

  74. Huang A, Abbasakoor F, Vaizey CJ (2006) Gastrointestinal manifestations of chronic granulomatous disease. Color Dis 8(8):637–644

    Article  CAS  Google Scholar 

  75. Barton LL, Moussa SL, Villar RG, Hulett RL (1998) Gastrointestinal complications of chronic granulomatous disease: case report and literature review. Clin Pediatr (Phila) 37(4):231–236

    Article  CAS  Google Scholar 

  76. Marks DJ et al (2009) Inflammatory bowel disease in CGD reproduces the clinicopathological features of Crohn’s disease. Am J Gastroenterol 104(1):117–124

    Article  CAS  PubMed  Google Scholar 

  77. Mulholland MW, Delaney JP, Simmons RL (1983) Gastrointestinal complications of chronic granulomatous disease: surgical implications. Surgery 94(4):569–575

    CAS  PubMed  Google Scholar 

  78. Alimchandani M, Lai JP, Aung PP, Khangura S, Kamal N, Gallin JI, Holland SM, Malech HL, Heller T, Miettinen M, Quezado MM (2013) Gastrointestinal histopathology in chronic granulomatous disease: a study of 87 patients. Am J Surg Pathol 37(9):1365–1372

    Article  PubMed  PubMed Central  Google Scholar 

  79. Yu JE, de Ravin SS, Uzel G, Landers C, Targan S, Malech HL, Holland SM, Cao W, Harpaz N, Mayer L, Cunningham-Rundles C (2011) High levels of Crohn’s disease-associated anti-microbial antibodies are present and independent of colitis in chronic granulomatous disease. Clin Immunol 138(1):14–22

    Article  CAS  PubMed  Google Scholar 

  80. Uzzan M, Ko HM, Mehandru S, Cunningham-Rundles C (2016) Gastrointestinal disorders associated with common variable immune deficiency (CVID) and chronic granulomatous disease (CGD). Curr Gastroenterol Rep 18(4):17

    Article  PubMed  PubMed Central  Google Scholar 

  81. Rieber N et al (2012) Current concepts of hyperinflammation in chronic granulomatous disease. Clin Dev Immunol 2012:252460

    Article  PubMed  Google Scholar 

  82. Meissner F, Seger RA, Moshous D, Fischer A, Reichenbach J, Zychlinsky A (2010) Inflammasome activation in NADPH oxidase defective mononuclear phagocytes from patients with chronic granulomatous disease. Blood 116(9):1570–1573

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  83. Kuijpers T, Lutter R (2012) Inflammation and repeated infections in CGD: two sides of a coin. Cell Mol Life Sci 69(1):7–15

    Article  CAS  PubMed  Google Scholar 

  84. Crowley CA, Curnutte JT, Rosin RE, André-Schwartz J, Gallin JI, Klempner M, Snyderman R, Southwick FS, Stossel TP, Babior BM (1980) An inherited abnormality of neutrophil adhesion. Its genetic transmission and its association with a missing protein. N Engl J Med 302(21):1163–1168

    Article  CAS  PubMed  Google Scholar 

  85. Arnaout MA (1990) Leukocyte adhesion molecules deficiency: its structural basis, pathophysiology and implications for modulating the inflammatory response. Immunol Rev 114:145–180

    Article  CAS  PubMed  Google Scholar 

  86. Hanna S, Etzioni A (2012) Leukocyte adhesion deficiencies. Ann N Y Acad Sci 1250:50–55

    Article  CAS  PubMed  Google Scholar 

  87. Movahedi M, Entezari N, Pourpak Z, Mamishi S, Chavoshzadeh Z, Gharagozlou M, Mir-Saeeid-Ghazi B, Fazlollahi MR, Zandieh F, Bemanian MH, Farhoudi A, Aghamohammadi A (2007) Clinical and laboratory findings in Iranian patients with leukocyte adhesion deficiency (study of 15 cases). J Clin Immunol 27(3):302–307

    Article  PubMed  Google Scholar 

  88. Jain S, Gozdziak P, Morgan A, Burt RK (2013) Remission of Crohn’s disease after cord blood transplantation for leukocyte adhesion deficiency type 1. Bone Marrow Transplant 48(7):1006–1007

    Article  CAS  PubMed  Google Scholar 

  89. Jain AK, Motil KJ, Abramson SL, Han YS, Tatevian N (2010) Rectal ulcer with an elusive diagnosis: all that ulcers is not Crohn disease. J Pediatr Gastroenterol Nutr 51(3):367–369

    Article  PubMed  Google Scholar 

  90. D'Agata ID, Paradis K, Chad Z, Bonny Y, Seidman E (1996) Leucocyte adhesion deficiency presenting as a chronic ileocolitis. Gut 39(4):605–608

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  91. Uzel G, Kleiner DE, Kuhns DB, Holland SM (2001) Dysfunctional LAD-1 neutrophils and colitis. Gastroenterology 121(4):958–964

    Article  CAS  PubMed  Google Scholar 

  92. Boztug K, Appaswamy G, Ashikov A, Schäffer AA, Salzer U, Diestelhorst J, Germeshausen M, Brandes G, Lee-Gossler J, Noyan F, Gatzke AK, Minkov M, Greil J, Kratz C, Petropoulou T, Pellier I, Bellanné-Chantelot C, Rezaei N, Mönkemöller K, Irani-Hakimeh N, Bakker H, Gerardy-Schahn R, Zeidler C, Grimbacher B, Welte K, Klein C (2009) A novel syndrome with congenital neutropenia caused by mutations in G6PC3. N Engl J Med 360(1):32–43

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  93. Kaya Z et al (2014) Resolution of inflammatory colitis with pegfilgrastim treatment in a case of severe congenital neutropenia due to glucose 6 phosphatase catalytic subunit-3 deficiency. J pediatr Hem Onc 36(5):e316-e318

    Google Scholar 

  94. Desplantes C et al (2014) Clinic spectrum and long-term follow-up of 14 cases with G6PC3 mutations from the French severe congenital neutropenia registry. Orphanet J Rare Dis 183(9):1–15

    Google Scholar 

  95. Begin P et al (2013) Inflammatory bowel disease and T cell lymphopenia in G6PC3 deficiency. J Clin Immunol 33(3):520–525

    Article  CAS  PubMed  Google Scholar 

  96. Virdis F et al (2013) Heamophagocytic lymphohistiocytosis cased by primary Epstein-Barr virus in a patient with Crohn’s disease. World J Gastrrintest Surg 5(11):306–308

    Article  Google Scholar 

  97. Thompson, G., PepperellD., LawrenceI., McGettiganB.D. (2017) Crohn’s disease complicated by Epstein-Barr virus-driven haemophagocytic lymphohistiocytosis successfully treated with rituximab. BMJ Case Rep

  98. Li Y, Xia X, Zhang J, Song Z, Zhou L, Zhang Y, Huang Y, Shi Y, Quigley EM, Ding S (2015) Haemophagocyticlymphohistiocytosis in inflammatory bowel disease with virus infection. Prz Gastroenterol 10(2):78–82

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  99. Speckmann C et al (2013) X-linked inhibitor of apoptosis (XIAP) deficiency: the spectrum of presenting manifestations beyond hemophagocytic lymphohistiocytosis. Clin Immunol 149(1):133–141

    Article  CAS  PubMed  Google Scholar 

  100. Henter JI, Elinder G, Ost A (1991) Diagnostic guidelines for hemophagocytic lymphohistiocytosis. The FHL Study Group of the Histiocyte Society. Semin. Oncol 18(1):29–33

    CAS  PubMed  Google Scholar 

  101. Brito-Zeron P et al (2016) Infection is the major trigger of hemophagocytic syndrome in adult patients treated with biological therapies. Semin Arthritis Rheum 45(4):391–399

    Article  PubMed  Google Scholar 

  102. Hyams J et al (2017) Infliximab is not associated with increased risk of malignancy or hemophagocytic lymphohistiocytosis in pediatric patients with inflammatory bowel disease. Gastroenterol 152(8):1901–1914

    Article  Google Scholar 

  103. Vogel, G., et al. (2017) Disrupted apical exocytosis of cargo vesicles causes enteropathy in FHL5 patients with Munc18-2 mutations. JCI Insight. 2(Jul (14)): p. [Epub ahead of print]

  104. Speckmann C, Ehl S (2014) XIAP deficiency is a mendelian cause of late-onset IBD. Gut 63(6):1031–1032

    Article  PubMed  Google Scholar 

  105. Aguilar C, Latour S (2015) X-linked inhibitor of apoptosis protein deficiency: more than X-linked lymphoproliferative syndrome. J Clin Immunol 35(4):331–338

    Article  CAS  PubMed  Google Scholar 

  106. Pachlopnik S et al (2011) Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency). Blood 117(5):1522–1529

    Article  CAS  Google Scholar 

  107. Nielsen OH, LaCasse EC (2017) How genetic testing can lead to targeted management of XIAP deficiency-related inflammatory bowel disease. Genet Med 19(Feb 92):133–143

    Article  PubMed  Google Scholar 

  108. Schubert D et al (2014) Autosomal-dominant immune dysregulation syndrome in humans with CTLA4 mutations. Nat Med 20(12):1410–1416

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  109. Friedline R et al (2009) CD4+ regulatory T cells require CTLA-4 for the maintenance of systemic tolerance. J Exp Med 206(2):421–434

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  110. Wing K et al (2008) CTLA-4 control over Foxp3+ regulatory T cell function. Science 322(5899):271–275

    Article  CAS  PubMed  Google Scholar 

  111. Walker L, Sansom D (2011) The emerging role of CTLA4 as a cell-extrinsic regulator of T cell responses. Nat Rev Immnol 11:852–863

    Article  CAS  Google Scholar 

  112. Moraes-Fontes M et al (2017) Fatal CTLA-4 heterozygosity with autoimmunity and recurrent infections: a de novo mutation. Clin Case Rep 5(12):2066–2070

    Article  PubMed  PubMed Central  Google Scholar 

  113. Kuehn H et al (2014) Immune dysregulation in human subjects with heterozygous germline mutations in CTLA4. Science 345(6024):1623–1627

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  114. Lee S et al (2016) Abatacept alleviates severe autoimmune symptoms in a patient carrying a de novo variant in CTLA-4. J Allergy Clin Immunol 137(1):327–330

    Article  PubMed  Google Scholar 

  115. Lo B et al (2016) CHAI and LATAIE: new genetic disease of CTLA-4 checkpoint insufficiency. Blood 128(8):1037–1042

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  116. Lo B et al (2015) Patients with LRBA deficiency show CTLA4 loss and immune dysregulation responsive to abatacept therapy. Science 349(6246):436–440

    Article  CAS  PubMed  Google Scholar 

  117. Gamez-Diaz L et al (2016) The extended phenotype of LPS-responsive beige-like anchor protein (LRBA) deficiency. J Allergy Clin Immunol 137(1):223–230

    Article  CAS  PubMed  Google Scholar 

  118. Fu X (2006) STAT3 in immune responses and inflammatory bowel disease. Cell Res 16(2):214–219

    Article  CAS  PubMed  Google Scholar 

  119. Haapaniemi E et al (2015) Autoimmunity, hypogammaglobulinema, lymphoproliferation, and mycobacterial disease in patients with activating mutations in STAT3. Blood 125(4):639–648

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  120. Holland S et al (2007) STAT3 mutations in the hyper-IgE syndrome. NEJM 357(16):1058–1062

    Article  Google Scholar 

  121. Milner JD et al (2015) Early-onset lymphoproliferation and autoimmunity caused by germline STAT3 gain-of-function mutations. Blood 125(4):591–599

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  122. Minegishi Y et al (2007) Dominant-negative mutations in the DNA-binding domain of STAT3 cause hyper-IgE syndrome. Nature 448(7157):1058–1062

    Article  CAS  PubMed  Google Scholar 

  123. Uzel G, Sampaio EP, Lawrence MG, Hsu AP, Hackett M, Dorsey MJ, Noel RJ, Verbsky JW, Freeman AF, Janssen E, Bonilla FA, Pechacek J, Chandrasekaran P, Browne SK, Agharahimi A, Gharib AM, Mannurita SC, Yim JJ, Gambineri E, Torgerson T, Tran DQ, Milner JD, Holland SM (2013) Dominant gain-of-function STAT1 mutations in FOXP3 wild-type immune dysregulation-polyendocrinopathy-enteropathy-X-linked-like syndrome. J Allergy Clin Immunol 131(6):1611–1623

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  124. Engelhardt KR et al (2013) Clnical outcome in IL-10 and IL-10 receptor-deficient patients with or without hematopoietic cell transplantation. J Allergy Clin Immunol 131(3):825–830

    Article  CAS  PubMed  Google Scholar 

  125. Glocker EO, Frede N, Perro M, Sebire N, Elawad M, Shah N, Grimbacher B (2010) Infant colitis—it’s in the genes. Lancet 376(9748):1272

    Article  PubMed  Google Scholar 

  126. Kotlarz D, Beier R, Murugan D, Diestelhorst J, Jensen O, Boztug K, Pfeifer D, Kreipe H, Pfister E–D, Baumann U, Puchalka J, Bohne J, Egritas O, Dalgic B, Kolho K–L, Sauerbrey A, Buderus S, Güngör T, Enninger A, Koda YKL, Guariso G, Weiss B, Corbacioglu S, Socha P, Uslu N, Metin A, Wahbeh GT, Husain K, Ramadan D, al–Herz W, Grimbacher B, Sauer M, Sykora K–W, Koletzko S, Klein C (2012) Loss of interluken-10 signaling and infantile inflammatory bowel disease-implications for diagnosis and therapy. Gastroenterology 143:347–355

    Article  CAS  PubMed  Google Scholar 

  127. Mao H, Yang W, Lee PPW, Ho MHK, Yang J, Zeng S, Chong CY, Lee TL, Tu W, Lau YL (2012) Exome sequencing indentifies novel compound heterozygous mutations of IL-1 receptor 1 in neonatal onset Crohn’s disease. Genes Immun 13:437–442

    Article  CAS  PubMed  Google Scholar 

  128. Salzer E, Kansu A, Sic H, Májek P, Ikincioğullari A, Dogu FE, Prengemann NK, Santos-Valente E, Pickl WF, Bilic I, Ban SA, Kuloğlu Z, Demir AM, Ensari A, Colinge J, Rizzi M, Eibel H, Boztug K (2014) Early-onset inflammatory bowel disease and common variable immunodeficiency-like disease caused by IL-21 deficiency. J Allergy Clin Immunol 133(6):1651–1659

    Article  CAS  PubMed  Google Scholar 

  129. Ochs H, Thrasher A (2006) The Wiskott-Aldrich syndrome. J Allergy Clin Immunol 117:725–738

    Article  CAS  PubMed  Google Scholar 

  130. Derry J, Ochs H, Francke U (1994) Isolation of a novel gene mutated in Wiskott-Aldrich syndrome. Cell 79(5):922

    Google Scholar 

  131. Kim A et al (2000) Autoinhibition and activation mechanisms of the Wiskott-Aldrich syndrome protein. Nature 404:151–158

    Article  CAS  PubMed  Google Scholar 

  132. Jin Y, Mazza C, Christie JR, Giliani S, Fiorini M, Mella P, Gandellini F, Stewart DM, Zhu Q, Nelson DL, Notarangelo LD, Ochs HD (2004) Mutations of the Wiskott-Aldrich Syndrome Protein (WASP): hotspots, effect on transcription, and translation and phenotype/genotype correlation. Blood 104(13):4010–4019

    Article  CAS  PubMed  Google Scholar 

  133. Devriendt K, Kim AS, Mathijs G, Frints SGM, Schwartz M, van den Oord JJ, Verhoef GEG, Boogaerts MA, Fryns JP, You D, Rosen MK, Vandenberghe P (2001) Constitutively activating mutation in WASP causes X-linked severe congenital neutropenia. Nat Genet 27(3):313–317

    Article  CAS  PubMed  Google Scholar 

  134. Dupuis-Girod S, Medioni J, Haddad E, Quartier P, Cavazzana-Calvo M, le Deist F, de Saint Basile G, Delaunay J, Schwarz K, Casanova JL, Blanche S, Fischer A (2003) Autoimmunity in Wiskott-Aldrich syndrome: risk factors, clinical features and outcome in a single center cohort of 55 patients. Pediatrics 111:e622–e627

    Article  PubMed  Google Scholar 

  135. Candotti F (2018) Clinical manifestations and pathophysiological mechanisms of the Wiskott-Aldrich syndrome. J Clin Immunol 38:13–27

    Article  CAS  PubMed  Google Scholar 

  136. Ngwube, A., et al. (2017) Outcomes after allogeneic transplant in patients with Wiskott-Aldrich syndrome. Biol Blood Marrow Transplant (17): p. Epub ahead of print

  137. Chen N, Zhang ZY, Liu DW, Liu W, Tang XM, Zhao XD (2015) The clinical features of autoimmunity in 53 patients with Wiskott-Aldrich syndrome in China: a single-center study. Eur J Pediatr 174:1311–1318

    Article  CAS  PubMed  Google Scholar 

  138. Afazali B et al (2017) BACH2 immunodeficiency illustrates an association between super-enhancers and haploinsufficiency. Nat Immunol 18(7):813–823

    Article  CAS  Google Scholar 

  139. Conrad MA, Dawany N, Sullivan KE, Devoto M, Kelsen JR (2017) Novel ZBTB24 mutation associated with immunodeficiency, centromere instability, and facial anomalies type-2 syndrome identified in a patient with very early onset inflammatory bowel disease. Inflamm Bowel Dis 23(12):2252–2255

    Article  PubMed  Google Scholar 

  140. Boland BS, Widjaja CE, Banno A, Zhang B, Kim SH, Stoven S, Peterson MR, Jones MC, Su HI, Crowe SE, Bui JD, Ho SB, Okugawa Y, Goel A, Marietta EV, Khosroheidari M, Jepsen K, Aramburu J, López-Rodríguez C, Sandborn WJ, Murray JA, Harismendy O, Chang JT (2015) Immunodeficiency and autoimmune enterocolopathy linked to NFAT5 haploinsufficiency. J Immunol 194(6):2551–2560

    Article  CAS  PubMed  Google Scholar 

  141. Nagamine K, Peterson P, Scott HS, Kudoh J, Minoshima S, Heino M, Krohn KJE, Lalioti MD, Mullis PE, Antonarakis SE, Kawasaki K, Asakawa S, Ito F, Shimizu N (1997) Positional cloning of the APECED gene. Nat Genet 17:393–398

    Article  CAS  PubMed  Google Scholar 

  142. Kluger N, Jokinen M, Krohn K, Ranki A (2013) Gastrointestinal manifestations in APECED syndrome. J Clin Gastroenterol 47(2):112–120

    Article  CAS  PubMed  Google Scholar 

  143. Chida N, Kobayashi I, Takezaki S, Ueki M, Yamazaki Y, Garelli S, Scarpa R, Horikawa R, Yamada M, Betterle C, Notarangelo LD, Yawaka Y, Ariga T (2015) Disease specificity of anti-tryptophan hydroxylase-1 and anti-AIE-75 autoantibodies in APECED and IPEX syndrome. Clin Immunol 156(1):36–42

    Article  CAS  PubMed  Google Scholar 

  144. Lohr N et al (2010) Human ITCH E3 ubiquitin ligase deficiency causes syndromic multisystem autoimmune disease. Am J Hum Genet 86(3):447–453

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  145. Jeon M et al (2004) Essential role of the E3 ubiquitin ligase Cbl-b in T cell anergy induction. Immunity 21:167–177

    Article  CAS  PubMed  Google Scholar 

  146. Romberg N, al Moussawi K, Nelson-Williams C, Stiegler AL, Loring E, Choi M, Overton J, Meffre E, Khokha MK, Huttner AJ, West B, Podoltsev NA, Boggon TJ, Kazmierczak BI, Lifton RP (2014) Mutation of NLRC4 causes a syndrome of enterocolitis and autoinflammation. Nat Genet 46(10):1135–1139

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  147. Canna SW, Girard C, Malle L, de Jesus A, Romberg N, Kelsen J, Surrey LF, Russo P, Sleight A, Schiffrin E, Gabay C, Goldbach-Mansky R, Behrens EM (2017) Life-threatening NLRC4-associated hyperinflammation successfully treated with IL-18 inhibition. J Allergy Clin Immunol 139(5):1698–1701

    Article  CAS  PubMed  Google Scholar 

  148. Jorgensen S et al (2016) Altered gut microbiota profile in common variable immunodeficiency associates with levels of lipopolysaccharide and markers of systemic immune activation. Mucossal Immunol 9(6):1455–1465

    Article  CAS  Google Scholar 

  149. Cordova Guevara H, Guarner Aguilar L (2009) Effective treatment of common variable immunodeficiency associated diarrhea. Rev Esp Enferm Dig 101(3):215–219

    Article  CAS  PubMed  Google Scholar 

  150. Malamut G, Verkarre V, Suarez F, Viallard JF, Lascaux AS, Cosnes J, Bouhnik Y, Lambotte O, Béchade D, Ziol M, Lavergne A, Hermine O, Cerf-Bensussan N, Cellier C (2010) The enteropathy associated with common variable immunodeficiency: the delineated frontiers with celiac disease. Am J Gastroenterol 105(10):2262–2275

    Article  CAS  PubMed  Google Scholar 

  151. Kralickova P, Mala E, Vokurkova D, Krcmova I, Pliskova L, Stepanova V, Bartos V, Koblizek V, Tacheci I, Bures J, Brozik J, Litzman J (2014) Cytomegalovirus disease in patients with common variable immunodeficiency: three case reports. Int Arch Allergy Immunol 163(1):69–74

    Article  PubMed  Google Scholar 

  152. Salcedo J, Keates S, Pothoulakis C, Warny M, Castagliuolo I, LaMont JT, Kelly CP (1997) Intravenous immunoglobulin therapy for severe Clostridium difficile colitis. Gut 41(3):366–370

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  153. Woodward JM, Gkrania-Klotsas E, Cordero-Ng AYK, Aravinthan A, Bandoh BN, Liu H, Davies S, Zhang H, Stevenson P, Curran MD, Kumararatne D (2015) The role of chronic norovirus infection in the enteropathy associated with common variable immunodeficiency. Am J Gastroenterol 110(2):320–327

    Article  CAS  PubMed  Google Scholar 

  154. van de Ven AA et al (2014) Increased prevalence of gastrointestinal viruses and diminished secretory immunoglobulin a levels in antibody deficiencies. J Clin Immunol 34(8):962–970

    Article  PubMed  CAS  Google Scholar 

  155. Fabre A et al (2014) Syndrome (phenotypic) diarrhoea of infancy/tricho-hepato-enteric syndrome. Arch Dis Child 99(1):35–38

    Article  PubMed  Google Scholar 

  156. Girault D et al (1994) Intractable infant diarrhea associated with phenotypic abnormalities and immunodeficiency. J Pediatr 125(1):36–42

    Article  CAS  PubMed  Google Scholar 

  157. Hartley J et al (2010) Mutations in TTC37 cause tricohepatoenteric syndrome (phenotypic diarrhea of infancy). Gastroenterology 138(7):2388–2398

    Article  CAS  PubMed  Google Scholar 

  158. Fabre A et al (2012) SKIV2L mutations cause syndromic diarrhea, or trichohepatoenteric syndrome. Am J Hum Genet 90(4):689–692

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  159. Stepensky P et al (2013) Persistent defective membrane trafficking in epithelial cells of patients with familial hemophagocytic lymphohystiocytosis type 5 due to STXBP2/MUNC18-2 mutations. Pediatr Blood Cancer 60(7):1215–1222

    Article  CAS  PubMed  Google Scholar 

  160. Pagel J et al (2010) Distinct mutations in STXBP2 are associated with variable clinical presentations in patients with familial hemophagocytic lymphohistiocytosis type 5 (FHL5). Blood 119(25):6016–6024

    Article  CAS  Google Scholar 

  161. de la Morena MT, Leonard D, Torgerson TR, Cabral-Marques O, Slatter M, Aghamohammadi A, Chandra S, Murguia-Favela L, Bonilla FA, Kanariou M, Damrongwatanasuk R, Kuo CY, Dvorak CC, Meyts I, Chen K, Kobrynski L, Kapoor N, Richter D, DiGiovanni D, Dhalla F, Farmaki E, Speckmann C, Español T, Shcherbina A, Hanson IC, Litzman J, Routes JM, Wong M, Fuleihan R, Seneviratne SL, Small TN, Janda A, Bezrodnik L, Seger R, Raccio AG, Edgar JDM, Chou J, Abbott JK, van Montfrans J, González-Granado LI, Bunin N, Kutukculer N, Gray P, Seminario G, Pasic S, Aquino V, Wysocki C, Abolhassani H, Dorsey M, Cunningham-Rundles C, Knutsen AP, Sleasman J, Costa Carvalho BT, Condino-Neto A, Grunebaum E, Chapel H, Ochs HD, Filipovich A, Cowan M, Gennery A, Cant A, Notarangelo LD, Roifman CM (2017) Long-term outcomes of 176 patients with X-linked hyper-IgM syndrome treated with or without hematopoietic cell transplantation. J Allergy Clin Immunol 139(4):1282–1292

    Article  PubMed  CAS  Google Scholar 

  162. Albuquerque A (2014) Nodular lymphoid hyperplasia in the gastrointestinal tract in adult patients: a review. World J Gastroenterol 6(11):534–540

    Google Scholar 

  163. Ranchod M, Lewkin K, Dorfman R (1978) Lymphoid hyperplasia of the gastrointestinal tract.A study of 26 cases and review of the literature. Am J Surg Pathol 2:383–400

    Article  CAS  PubMed  Google Scholar 

  164. Colon A, DiPalma J, Leftridge C (1991) Intestinal lympho-nodular hyperplasia of childhood: patterns of presentation. J Clin Gastroenterol 13:163–166

    Article  CAS  PubMed  Google Scholar 

  165. Rambaud J et al (1982) Diffuse follicular lymphoid hyperplasia of the small intestine without primary antibody deficiency. Am J Med 73:125–132

    Article  CAS  PubMed  Google Scholar 

  166. Joo M, Shim SH, Chang SH, Kim H, Chi JG, Kim NH (2009) Nodular lymphoid hyperplasia and histologic changes mimicking celiac disease, collagenous sprue, and lymphocytic colitis in a patient with selective IgA deficiency. Pathol Res Pract 205(12):876–880

    Article  PubMed  Google Scholar 

  167. Schwartz D, Cole CE, Sun Y, Jacoby RF (2003) Diffuse nodular lymphoid hyperplasia of the colon: polyposis syndrome or normal variant? Gastrointest Endosc 58:630–632

    PubMed  Google Scholar 

  168. Rubio-Tapia A, Hernández-Calleros J, Trinidad-Hernández S, Uscanga L (2006) Clinical characteristics of a group of adults with nodular lymphoid hyperplasia: a single center experience. World J Gastroenterol 12:1945–1948

    Article  PubMed  PubMed Central  Google Scholar 

  169. Hermans P et al (1966) Dysgammaglobulinemia associated with nodular lymphoid hyperplasia of the small intestine. Am J Med 40:78–89

    Article  CAS  PubMed  Google Scholar 

  170. Khuroo M, Khuroo N, Khuroo M (2011) Diffuse duodenal nodular lymphoid hyperplasia: a large cohort of patients etiologically related to Helicobacter pylori infection. BMC Gastroentrol 11(36):1–11

    Google Scholar 

  171. Hanich T, Majnarić L, Janković D, Šabanović Š, Včev A (2017) Nodular lymphoid hyperplasia complicated with ileal Burkitt’s lymphoma in an adult patient with selective IgA deficiency. Int J Surg Case Rep 30:69–72

    Article  PubMed  Google Scholar 

  172. Collin P, Mäki M, Keyriläinen O, Hällström O, Reunala T, Pasternack A (1992) Selective IgA deficiency and coeliac disease. Scand J Gastroenterol 27:367–371

    Article  CAS  PubMed  Google Scholar 

  173. Ouakaa-Kchaou A, Trad D, Boussourra H, Bibani N, Elloumi H, Kochlef A, Gargouri D, Kharrat J (2015) Hypogammaglobulinemia associated with nodular lymphoid hyperplasia of the intestine and pernicious anaemia. Tunis Med 93(11):662–664

    PubMed  Google Scholar 

  174. Webster AD, Kenwright S, Ballard J, Shiner M, Slavin G, Levi AJ, Loewi G, Asherson GL (1977) Nodular lymphoid hyperplasia of the bowel in primary hypogammaglobulinaemia: study of in vivo and in vitro lymphocyte function. Gut 18(5):364–372

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  175. Bayraktar Y, Ersoy O, Sokmensuer C (2007) The findings of capsule endoscopy in patients with common variable immunodeficiency syndrome. Hepato-Gastroenterology 54(76):1034–1037

    PubMed  Google Scholar 

  176. Van den Brande P et al (1988) Intestinal nodular lymphoid hyperplasia in patients with common variable immunodeficiency: local accumulation of B and CD8(+) lymphocytes. J Clin Immunol 8(4):296–306

    Article  PubMed  Google Scholar 

  177. Rodrigues F, Graham Davies E, Harrison P, McLauchlin J, Karani J, Portmann B, Jones A, Veys P, Mieli-Vergani G, Hadžić N (2004) Liver disease in children with primary immunodeficiencies. J Pediatr 145(3):333–339

    Article  PubMed  Google Scholar 

  178. van den Berge J et al (2009) Chronic granulomatous disease:the European experience. PLoS One 4(4):e5234

    Article  CAS  Google Scholar 

  179. Hussain N et al (2007) Hepatic abnormalities in patients with chronic granulomatous disease. Hepatology 45(3):675–683

    Article  PubMed  Google Scholar 

  180. Levy J, Espanol-Boren T, Thomas C, Fischer A, Tovo P, Bordigoni P, Resnick I, Fasth A, Baer M, Gomez L, Sanders EAM, Tabone MD, Plantaz D, Etzioni A, Monafo V, Abinun M, Hammarstrom L, Abrahamsen T, Jones A, Finn A, Klemola T, DeVries E, Sanal O, Peitsch MC, Notarangelo LD (1997) Clinical spectrum of X-linked hyper-IgM syndrome. J Pediatr 131(1 Pt 1):47–54

    Article  CAS  PubMed  Google Scholar 

  181. Durandy A et al (2013) Potential roles of activation-induced cytidine deaminase in promotion or prevention of autoimmunity in humans. Autoimmunity 46(2):148–156

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  182. de Pontual L et al (2007) Epistatic interactions with a common hypomorphic RET allele in syndromic Hirschprung disease. Hum Mutat 28(8):790–796

    Article  PubMed  CAS  Google Scholar 

  183. Makitie O et al (2002) Hirschprung’s disease in cartilage-hairhypoplasia has poor prognosis. J Pediatr Surg 37(11):1585–1588

    Article  PubMed  Google Scholar 

  184. Digilio MC, Marino B, Bagolan P, Giannotti A, Dallapiccola B (1999) Microdeletion 22q11 and oesophageal atresia. J Med Genet 36(2):137–139

    CAS  PubMed  PubMed Central  Google Scholar 

  185. Arora M, Bagi P, Strongin A, Heimall J, Zhao X, Lawrence MG, Trivedi A, Henderson C, Hsu A, Quezado M, Kleiner DE, Venkatesan AM, Holland SM, Freeman AF, Heller T (2017) Gastrointestinal manifestations of STAT3-deficient hyper-IgE syndrome. J Clin Immunol 37(7):695–700

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  186. Chen R et al (2013) Whole-exome sequencing identifies tetratricopeptide repeat domain 7A (TTC7A) mutations for combined immunodeficiency with intestinal atresias. J Allergy Clin Immunol 132(3):656–664 e17

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  187. Samuels ME, Majewski J, Alirezaie N, Fernandez I, Casals F, Patey N, Decaluwe H, Gosselin I, Haddad E, Hodgkinson A, Idaghdour Y, Marchand V, Michaud JL, Rodrigue MA, Desjardins S, Dubois S, le Deist F, Awadalla P, Raymond V, Maranda B (2013) Exome sequencing identifies mutations in the gene TTC7A in French-Canadian cases with hereditary multiple intestinal atresia. J Med Genet 50(5):324–329

    Article  CAS  PubMed  Google Scholar 

  188. Guttman FM, Braun P, Garance PH, Blanchard H, Collin PP, Dallaire L, Desjardins JG, Perreault G (1973) Multiple atresias and a new syndrome of hereditary multiple atresias involving the gastrointestinal tract from stomach to rectum. J Pediatr Surg 8(5):633–640

    Article  CAS  PubMed  Google Scholar 

  189. Mishalany HG, Der Kaloustian VM (1971) Familial multiple-level intestinal atresias: report of two siblings. J Pediatr 79(1):124–125

    Article  CAS  PubMed  Google Scholar 

  190. Moreno LA, Gottrand F, Turck D, Manouvrier-Hanu S, Mazingue F, Morisot C, le Deist F, Ricour C, Nihoul-Feketé C, Debeugny P, Griscelli C, Farriaux JP (1990) Severe combined immunodeficiency syndrome associated with autosomal recessive familial multiple gastrointestinal atresias: study of a family. Am J Med Genet 37(1):143–146

    Article  CAS  PubMed  Google Scholar 

  191. Rothenberg ME, White FV, Chilmonczyk B, Chatila T (1995) A syndrome involving immunodeficiency and multiple intestinal atresias. Immunodeficiency 5(3):171–178

    CAS  PubMed  Google Scholar 

  192. Ali, Y.A., et al. (2011) Hereditary multiple intestinal atresia (HMIA) with severe combined immunodeficiency (SCID): a case report of two siblings and review of the literature on MIA, HMIA and HMIA with immunodeficiency over the last 50 years. BMJ Case Rep 2011

  193. Lavilla P et al (1993) X-lined agammaglobulinemia and gastric adenocarcinoma. Cancer 72(5):1528–1531

    Article  CAS  PubMed  Google Scholar 

  194. Page A, Hansen A, Good R (1963) Occurrence of leukemia and lymphoma in patients with agammaglobulinemia. Blood 21(2):197–206

    Article  CAS  PubMed  Google Scholar 

  195. Mortaz E et al (2016) Cancers related to immunodeficiencies: update and perspectives. Front Immunol 7:1–13

    Article  CAS  Google Scholar 

  196. Agarwal S, Mayer L (2009) Pathogenesis and treatment of gastrointestinal disese in antibody deficiency syndromes. J Allergy Clin Immunol 124(4):658–664

    Article  CAS  PubMed  Google Scholar 

  197. Conley ME, Ziegler MM, IV SB, Huff DS, Boyle JT (1988) Multifocal adenocarcinoma of the stomach in a child with common variable immunodeficiency. J Pediatr Gastroenterol Nutr 7(3):456–460

    Article  CAS  PubMed  Google Scholar 

  198. van der Meer J et al (1993) Colorectal cancer in patients with X-linked agammaglobulinemia. Lancet 341:1439–1440

    Article  PubMed  Google Scholar 

  199. Levin E et al (2016) Hyper IgM syndrome: a report from the USIDNET Registry. J Clin Immunol 36:490–501

    Article  CAS  Google Scholar 

  200. Donaldson GP, Lee SM, Mazmanian SK (2016) Gut biogeography of the bacterial microbiota. Nat Rev Microbiol 14(1):20–32

    Article  CAS  PubMed  Google Scholar 

  201. Lamers CB et al (1980) Jejunal lymphoma in a patient with primary adult-onset hypogammaglobulinemia and nodular lymphoid hyperplasia of the small intestine. Dig Dis Sci 25(7):553–557

    Article  CAS  PubMed  Google Scholar 

  202. Casetellano G et al (1992) Malignant lymphoma of jejunum with common variable hypogammaglobulinemia and diffuse nodular lymphoid hyperplasia of the small intestine. A case study and literature review. J Clin Gastroenterol 15(2):128–135

    Article  Google Scholar 

  203. Eckburg PB, Bik EM, Bernstein CN, Purdom E, Dethlefsen L, Sargent M, Gill SR, Nelson KE, Relman DA (2005) Diversity of the human intestinal microbial flora. Science 308(5728):1635–1638

    Article  PubMed  PubMed Central  Google Scholar 

  204. Cummings JH, Pomare EW, Branch WJ, Naylor CP, Macfarlane GT (1987) Short chain fatty acids in human large intestine, portal, hepatic and venous blood. Gut 28(10):1221–1227

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  205. Furusawa Y, Obata Y, Fukuda S, Endo TA, Nakato G, Takahashi D, Nakanishi Y, Uetake C, Kato K, Kato T, Takahashi M, Fukuda NN, Murakami S, Miyauchi E, Hino S, Atarashi K, Onawa S, Fujimura Y, Lockett T, Clarke JM, Topping DL, Tomita M, Hori S, Ohara O, Morita T, Koseki H, Kikuchi J, Honda K, Hase K, Ohno H (2013) Commensal microbe-derived butyrate induces the differentiation of colonic regulatory T cells. Nature 504(7480):446–450

    Article  CAS  PubMed  Google Scholar 

  206. Arpaia N, Campbell C, Fan X, Dikiy S, van der Veeken J, deRoos P, Liu H, Cross JR, Pfeffer K, Coffer PJ, Rudensky AY (2013) Metabolites produced by commensal bacteria promote peripheral regulatory T-cell generation. Nature 504(7480):451–455

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  207. Rooks MG, Garrett WS (2016) Gut microbiota, metabolites and host immunity. Nat Rev Immunol 16(6):341–352

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  208. Thorburn AN, McKenzie CI, Shen S, Stanley D, Macia L, Mason LJ, Roberts LK, Wong CHY, Shim R, Robert R, Chevalier N, Tan JK, Mariño E, Moore RJ, Wong L, McConville MJ, Tull DL, Wood LG, Murphy VE, Mattes J, Gibson PG, Mackay CR (2015) Evidence that asthma is a developmental origin disease influenced by maternal diet and bacterial metabolites. Nat Commun 6:7320

    Article  CAS  PubMed  Google Scholar 

  209. Rider N et al (2009) Immunologic and clinical features of 25 Amish patients with RMRP 70 A→G cartilage hair hypoplasia. Clin Immunol 131(1):119–128

    Article  CAS  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Nicholas L. Rider.

Ethics declarations

Ethical Statement

This article is in compliance with the Journa’s ethical standards. Due to the nature of the review article, no patients were involved, and thus, informed consent was not applicable.

Conflict of Interest

The authors declare that they have no conflict of interest.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Hartono, S., Ippoliti, M.R., Mastroianni, M. et al. Gastrointestinal Disorders Associated with Primary Immunodeficiency Diseases. Clinic Rev Allerg Immunol 57, 145–165 (2019). https://doi.org/10.1007/s12016-018-8689-9

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12016-018-8689-9

Keywords

Navigation