CLINICAL HEPATITIS AFTER TRANSPLANTATION OF HEPATITIS-C VIRUS-POSITIVE KIDNEYS - HLA-DR3 AS A RISK FACTOR FOR THE DEVELOPMENT OF POSTTRANSPLANT HEPATITIS

Citation
Ad. Kirk et al., CLINICAL HEPATITIS AFTER TRANSPLANTATION OF HEPATITIS-C VIRUS-POSITIVE KIDNEYS - HLA-DR3 AS A RISK FACTOR FOR THE DEVELOPMENT OF POSTTRANSPLANT HEPATITIS, Transplantation, 62(12), 1996, pp. 1758-1762
Citations number
32
Categorie Soggetti
Immunology,Surgery,Transplantation
Journal title
ISSN journal
00411337
Volume
62
Issue
12
Year of publication
1996
Pages
1758 - 1762
Database
ISI
SICI code
0041-1337(1996)62:12<1758:CHATOH>2.0.ZU;2-H
Abstract
Background. Exposure to hepatitis C virus (HCV) and subsequent infecti on after renal transplantation lead to significant clinical hepatitis in approximately 50% of graft recipients, Methods. One hundred thirty- two consecutive renal allotransplant patients, who underwent transplan tation of kidneys from HCV-positive cadaveric donors, were studied to investigate the relationship between donor and recipient HLA type and the risk of developing clinical hepatitis, Specific attention was dire cted toward the DR3 and DR4 alleles, as these had previously been asso ciated with worse prognoses in autoimmune and viral hepatitis. Results , Overall, 42% of patients receiving kidneys from donors seropositive for HCV developed clinical hepatitis, This was unrelated to preoperati ve recipient HCV serum reactivity (P=0.65). Patients receiving kidneys from seropositive donors with HCV RNA as detected by PCR were more li kely to develop hepatitis than those receiving kidneys from PCR-negati ve donors (56% vs. 11%; P=0.005), The presence of the DR3 allele was a ssociated with a significant risk of clinical hepatitis (P=0.025); 80% of DR3-positive recipients (n=34) progressed to hepatitis compared wi th 42% of DR3-negative patients, No other recipient HLA type was signi ficantly related to prognosis. All patients receiving a donated kidney that expressed the B41 allele developed hepatitis, compared with 55% of recipients of non-B41 grafts (P=0.039). No association between the development of clinical hepatitis and HLA compatibility was found. Con clusions. These results suggest that both HLA type and viral presence as assayed by polymerase chain reaction, influence the risk. of diseas e progression after transplantation of HCV-positive kidneys, Applicati on of these associations may decrease the relative risk of a recipient contracting HCV hepatitis after cadaveric renal transplantation.