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Association of human cytomegalovirus viremia with human leukocyte antigens in liver transplantation recipients. | LitMetric

Association of human cytomegalovirus viremia with human leukocyte antigens in liver transplantation recipients.

Acta Biochim Biophys Sin (Shanghai)

State key Laboratory for Diagnosis and Treatment of Infectious Diseases, the First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, China.

Published: July 2011

AI Article Synopsis

  • The study focused on the relationship between HLA-matching and human cytomegalovirus (HCMV) infection after liver transplantation in patients with hepatitis B virus cirrhosis, reviewing data from 91 recipients.
  • Results showed a high incidence of HCMV infection (81.32%), with 17.6% of patients experiencing graft failure during the 4-year follow-up; however, HLA compatibility did not significantly affect the incidence of HCMV viremia or graft failure outcomes.
  • Interestingly, the study found that patients with better HLA-A compatibility had a higher risk of HCMV viremia, suggesting that HLA matching may not provide the expected protective effect in these

Article Abstract

Human cytomegalovirus (HCMV) reactivation is a common complication after liver transplantation (LT). Here, we investigated whether human leukocyte antigen (HLA)-matching was related to HCMV infection and subsequent graft failure after LT for hepatitis B virus  cirrhosis. This retrospective study reviewed 91 LT recipients. All the patients were grouped according to HLA-A, HLA-B, and HLA-DR locus matching. Clinical data were collected, including complete HLA-typing, HCMV viremia, graft failure, and the time of HCMV viremia. HLA typing was performed using a sequence-specific primer-polymerase chain reaction  kit. HCMV was detected by pp65 antigenemia using a commercial kit. The incidence of HCMV infection post-LT was 81.32%. Graft failure was observed in 16 of 91 (17.6%) patients during the 4-year study. The incidence of HCMV viremia was 100% (5/5), 91.4% (32/35), and 72.5% (37/51) in HLA-A two locus, one locus, and zero locus compatibility, respectively. Nevertheless, the degree of the HLA-A, HLA-B, or HLA-DR match did not influence the time of HCMV viremia, graft failure, or the time of graft failure after a diagnosis of HCMV viremia (all P > 0.05). An interesting discovery was that the risk of HCMV viremia tended to be higher in patients with better HLA-A compatibility. Graft failure, time of HCMV viremia, and graft failure after a diagnosis of HCMV viremia appear to be independent of HLA allele compatibility.

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Source
http://dx.doi.org/10.1093/abbs/gmr043DOI Listing

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