Characterization of occult hepatitis B virus from blood donors carrying genotype A2 or genotype D strains☆
Background/Aims
Nucleic acid testing (NAT) for hepatitis B virus (HBV) DNA in blood donations identified occult HBV infection (OBI) as a potential threat to blood safety.
Methods
A collaborative study was undertaken to explore the molecular basis of OBIs prevalent in Europe in relation to clinical and serological data.
Results
Ninety-one percent of 77 donor samples of European origin HBV DNA positive but HBV surface antigen (HBsAg) negative were confirmed. Viral load ranged between unquantifiable and 5640
IU/mL (median 25
IU/mL). Fifty-two strains were genotyped (14 HBVA2 and 38 HBVD). Compared to HBsAg+ samples, genotype D was significantly more frequent than genotype A2 in OBIs from Poland or Italy (P
<
0.04). Amino acid substitutions were concentrated in the immunologically active parts of the Pre-S/S proteins (P
<
0.0001) affecting both cellular CD8 T-cell epitopes and B-cell neutralizing Major Hydrophilic Region epitopes. Substitutions were more frequent in OBIs than in HBsAg+ strains of both genotype D (P
<
0.001) and A2 (P
<
0.01), in OBIs of genotype D than A2 in the ‘a’ region (P
<
0.001) but not cellular epitopes, and in anti-HBs+ than anti-HBs− OBIs (P
<
0.001).
Conclusions
Results support the hypothesis that humoral and cellular immune pressure on the HBV envelope proteins are major mechanisms generating OBI.
Keywords: Occult HBV, HBV, Blood donors, Europe
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☆ None of the co-authors has any conflict of interest to declare concerning the material presented in this manuscript. Dr. Allain is an occasional lecturer for the Chiron/Novartis Corporation.
PII: S0168-8278(08)00346-2
doi:10.1016/j.jhep.2008.04.017
© 2008 European Association for the Study of the Liver. Published by Elsevier Inc. All rights reserved.
