| Literature DB >> 26663521 |
Isabel Aguilera1, Maria José Martinez-Bravo1, Jose Manuel Sousa2, Antonio Jesús Pozo-Borrego1, Antonio Núñez-Roldán1.
Abstract
Although the pathogenic pathways leading to de novo immune hepatitis (IH) are not completely understood, we have shown strong evidences of an antidonor response against Glutathione S-transferase T1 (GSTT1), an antigen exclusively expressed in the donor liver. The first sign of this process is the production of GSTT1 antibodies that, in 25% of the cases, will precede de novo IH. Because the presence of the antibodies is not sufficient to trigger the disease, we aimed to study GSTT1 IgG subclasses in a group of 18 liver transplant patients, 12 that developed de novo IH and 6 that remained free of disease. Surprisingly, the predominant subclasses were IgG1-GSTT 1 and IgG4-GSTT 1. The presence of IgG4-expressing plasma cells was also investigated in 10 available liver biopsies. Six biopsies coinciding with diagnosis showed a mean value of 32.8 IgG4+ plasma cells/hpf vs. 5.55 in patients without the disease. We have not found a distinctive GSTT1-IgG profile in patients with de novo IH, but the ratio IgG1-GSTT 1 /IgG4-GSTT 1 in samples from close to the time of diagnosis seemed to be important. The novel finding of abundant IgG4-GSTT 1 in liver transplantation is intriguing, but their possible role in pathogenesis of de novo IH remains unknown.Entities:
Keywords: GSTT1 mismatch; IgG4-related diseases; donor-specific immune response; liver allograft rejection
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Year: 2016 PMID: 26663521 DOI: 10.1111/ctr.12675
Source DB: PubMed Journal: Clin Transplant ISSN: 0902-0063 Impact factor: 2.863