Abstract
Atypical anti-glomerular basement membrane (GBM) disease, which is characterized by low levels of or negativity for anti-GBM antibodies in circulation but positivity in the kidney, has been recognized in this decade. However, a therapeutic strategy has not been established to date because its outcome is better than that of classic anti-GBM disease. This case report and literature review highlight atypical anti-GBM disease in infection-related rapidly progressive glomerulonephritis. A 72-year-old Japanese man diagnosed with methicillin-susceptible Staphylococcus aureus (MSSA)-induced vertebral osteomyelitis experienced for 2 months was referred to our hospital because of renal insufficiency. He developed rapidly progressive glomerulonephritis with a serum creatinine level of 6.8 mg/dL, C-reactive protein level of 9.7 mg/dL, urinary protein-to-creatinine ratio of 3.37 g/gCr, and gross hematuria. The serum anti-GBM antibody concentration was 3.5 U/mL, which was slightly above the normal range (< 3.0 U/mL). Conservative treatment, mainly with antibiotics, improved the symptoms and renal function. The serum anti-GBM antibody concentration peaked at 4.0 U/mL on day 7 and decreased to an undetectable range at the end of eight-week antibiotic therapy. This is the first case report describing the presentation and disappearance of serum anti-GBM antibody in a patient with MSSA infection. Conservative treatment may be effective for patients with atypical anti-GBM disease complicated by infectious diseases.
Similar content being viewed by others
References
Goodpasture EW. Landmark publication from The American Journal of the Medical Sciences: the significance of certain pulmonary lesions in relation to the etiology of influenza. Am J Med Sci. 2009;338:148–51.
Li JN, Jia X, Wang Y, Xie C, Jiang T, Cui Z, et al. Plasma from patients with anti-glomerular basement membrane disease could recognize microbial peptides. PLoS ONE. 2017;12:e0174553.
McAdoo SP, Pusey CD. Anti-glomerular basement membrane disease. Clin J Am Soc Nephrol. 2017;12:1162–72.
Group KDIGOKGW. KDIGO clinical practice guideline for glomerulonephritis. Kidney Int. 2012;2(Supple 2):139–274.
Arimura Y, Muso E, Fujimoto S, Hasegawa M, Kaname S, Usui J, et al. Evidence-based clinical practice guidelines for rapidly progressive glomerulonephritis 2014. Clin Exp Nephrol. 2016;20:322–41.
Herody M, Bobrie G, Gouarin C, Grünfeld JP, Noel LH. Anti-GBM disease: predictive value of clinical, histological and serological data. Clin Nephrol. 1993;40:249–55.
Cui Z, Zhao MH, Singh AK, Wang HY. Antiglomerular basement membrane disease with normal renal function. Kidney Int. 2007;72:1403–8.
Nasr SH, Collins AB, Alexander MP, Schraith DF, Herrera Hernandez L, Fidler ME, et al. The clinicopathologic characteristics and outcome of atypical anti-glomerular basement membrane nephritis. Kidney Int. 2016;89:897–908.
Troxell ML, Houghton DC. Atypical anti-glomerular basement membrane disease. Clin Kidney J. 2016;9:211–21.
Gu QH, Xie LJ, Jia XY, Ma R, Liao YH, Cui Z, et al. Fever and prodromal infections in anti-glomerular basement membrane disease. Nephrology (Carlton). 2018;23:476–82.
Kashif W, Yaqub S, Mahmood SF, Patel J. Double-positive Goodpasture’s syndrome with concomitant active pulmonary tuberculosis. Saudi J Kidney Dis Transpl. 2013;24:783–8.
Lizarraga KJ, Florindez JA, Daftarian P, Andrews DM, Ortega LM, Mendoza JM, et al. Anti-GBM disease and ANCA during dengue infection. Clin Nephrol. 2015;83:104–10.
Mackintosh D, Mantha M, Oliver K. Goodpasture disease as a consequence of melioidosis. Intern Med J. 2016;46:1446–9.
Boardman EA, Sohail S, Yadavilli R. Goodpasture’s disease with late presentation of renal abnormality and anti-GBM autoantibody. BMJ Case Rep. 2017;2017:bcr2016218705.
Ossman R, Buob D, Hellmark T, Brocheriou I, Peltier J, Tamouza R, et al. Factors associated with pathogenicity of anti-glomerular basal membrane antibodies: a case report. Medicine (Baltimore). 2016;95:e3654.
Zijlstra HW, Mulder AHL, Geeraedts F, Visser F. Falsely positive anti-glomerular basement membrane antibodies in a patient with hantavirus induced acute kidney injury—a case report. BMC Nephrol. 2018;19:286.
Glassock RJ, Alvarado A, Prosek J, Hebert C, Parikh S, Satoskar A, et al. Staphylococcus-related glomerulonephritis and poststreptococcal glomerulonephritis: why defining “post” is important in understanding and treating infection-related glomerulonephritis. Am J Kidney Dis. 2015;65:826–32.
Berbari EF, Kanj SS, Kowalski TJ, Darouiche RO, Widmer AF, Schmitt SK, et al. 2015 Infectious Diseases Society of America (IDSA) clinical practice guidelines for the diagnosis and treatment of native vertebral osteomyelitis in adults. Clin Infect Dis. 2015;61:e26-46.
Csernok E, Holle JU. Twenty-eight years with antineutrophil cytoplasmic antibodies (ANCA): how to test for ANCA—evidence-based immunology? Auto Immun Highlights. 2010;1:39–43.
Salama AD, Dougan T, Levy JB, Cook HT, Morgan SH, Naudeer S, et al. Goodpasture’s disease in the absence of circulating anti-glomerular basement membrane antibodies as detected by standard techniques. Am J Kidney Dis. 2002;39:1162–7.
Usui J, Tanno M, Uehara R, Sanpei K, Maruyama K, Miyawaki H, et al. Evaluation of “STACIA MEBLux TEST GBM”, the novel diagnostic reagent for measurement of anti-GBM antibody using chemiluminescent enzyme immunoassay (CLEIA) (written in Japanese). Igakutoyakugaku. 2012;68:697–704.
Lewkowich IP, Campbell JD, HayGlass KT. Comparison of chemiluminescent assays and colorimetric ELISAs for quantification of murine IL-12, human IL-4 and murine IL-4: chemiluminescent substrates provide markedly enhanced sensitivity. J Immunol Methods. 2001;247:111–8.
Jia XY, Cui Z, Yang R, Hu SY, Zhao MH. Antibodies against linear epitopes on the Goodpasture autoantigen and kidney injury. Clin J Am Soc Nephrol. 2012;7:926–33.
Cui Z, Zhao MH, Xin G, Wang HY. Characteristics and prognosis of Chinese patients with anti-glomerular basement membrane disease. Nephron Clin Pract. 2005;99:c49-55.
Levy JB, Turner AN, Rees AJ, Pusey CD. Long-term outcome of anti-glomerular basement membrane antibody disease treated with plasma exchange and immunosuppression. Ann Intern Med. 2001;134:1033–42.
Zhao J, Yan Y, Cui Z, Yang R, Zhao MH. The immunoglobulin G subclass distribution of anti-GBM autoantibodies against rHalpha3(IV)NC1 is associated with disease severity. Hum Immunol. 2009;70:425–9.
Qu Z, Cui Z, Liu G, Zhao MH. The distribution of IgG subclass deposition on renal tissues from patients with anti-glomerular basement membrane disease. BMC Immunol. 2013;14:19.
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Conflict of interest
The authors declare that they have no conflict of interest.
Informed consent
Written informed consent was obtained from the patient for submitting this case report to English language journals.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Yamashita, T., Sato, K., Nishizawa, K. et al. Atypical anti-glomerular basement membrane disease complicated by methicillin-susceptible Staphylococcus aureus infection-related rapidly progressive glomerulonephritis: a case report and literature review. CEN Case Rep 10, 348–353 (2021). https://doi.org/10.1007/s13730-020-00564-9
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s13730-020-00564-9