4.4 Article

Role of G protein β3 subunit C825T and HLA class II polymorphisms in the immune response after HBV vaccination

Journal

VIROLOGY
Volume 297, Issue 2, Pages 245-252

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1006/viro.2002.1467

Keywords

lymphocyte proliferation; anti-HBs antibody; HBV; HLA-DQ; GNB3; G protein

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The G protein beta3 (GNB3) subunit and HLA are candidate genes predictive of immune response capacity. We therefore studied the influence of both gene systems on cellular and humoral immunity against hepatitis B virus (HBV) in 79 HBV booster-vaccinated healthy volunteers and an independent group of 77 probands after HBV basic immunization. Following booster vaccination, lymphocyte in vitro proliferation after stimulation with HBV surface antigen was 2.5-fold increased in GNB3 825T (TC + TT) vs CC allele carriers (P = 0.01) and was not influenced by HLA-DRB1 or DQB1 alleles. In addition, anti-HBs antibody titers in both groups were 2-fold increased in TC vs CC and decreased in TT vs CC allele carriers. However, antibody titers after HBV booster immunization were elevated in HLA-DQB1 *0301 carriers (P corrected = 0.027). In summary, the GN83 825T allele appears as a marker particularly predictive of cellular and HLA-DQB1*0301 of humoral immune responses following HBV vaccination. (C) 2002 Elsevier science (USA).

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