A case of bizarre posttransplant anti-glomerular basement membrane disease

• Main Authors: Anna Olewicz-Gawlik, Jan Żeromski, Monika Świerczewska, Ilona Idasiak-Piechocka, Magdalena Pawlik, Dorota Sikorska, Husam Samara, Andrzej Oko, Jan Sikora, Grzegorz Dworacki
• Format: Article
• Language: English
• Published: Termedia Publishing House 2019-07-01
• Series: Central European Journal of Immunology
• Subjects: anti-glomerular basement membrane disease; glomerulonephritis; kidney transplantation; immunofluorescence
• Online Access: https://www.termedia.pl/A-case-of-bizarre-posttransplant-anti-glomerular-basement-membrane-disease,10,37380,1,1.html
• ISSN: 1426-3912; 1644-4124

The non-collagenous (NC1) domain of 3 and 5 chains of type IV collagen are eminent targets of abnormal immune response in anti-glomerular basement membrane (anti-GBM) disease, which can be diagnosed by the presence of strong linear IgG staining along GBM detected by direct immunofluorescence. The presence of linear GBM fixation in renal allograft is a rare finding. We observed a 33-year-old male with de novo renal failure in a kidney transplant. An examination of a kidney biopsy specimen revealed, in light microscopy, mild mesangial hypercellularity together with mild focal interstitial fibrosis and sparse inflammatory infiltrate. In immunofluorescence microscopy strong linear IgG staining along the capillary walls was seen. Serum anti-GBM antibodies were negative and no mutation in exons coding NC1 domains of 3 and 5 chains of type IV collagen were detected. We described a rare case of a patient with atypical anti-GBM disease in renal allograft, caused probably by the same process which affected the native kidneys.