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J Hepatol. 2011 Dec 12. [Epub ahead of print]
T cell responses and viral variability in blood donation candidates with
occult hepatitis B infection.
Source:
http://www.ncbi.nlm.nih.gov/pubmed/22173156 Bes M, Vargas V, Piron M,
Casamitjana N, Esteban JI, Vilanova N, Pinacho A, Quer J, Puig L, Guardia
J, Sauleda S. SourceBanc de Sang i Teixits, Institut Català de la Salut,
Barcelona, Spain; Universitat Autònoma de Barcelona. Bellaterra, Spain;
Centro de investigación biomédica en red de enfermedades Hepáticas y
Digestivas (CIBEREHD) del Instituto de Salud Carlos III, Spain.
Abstract
BACKGROUND/AIMS: Occult HBV infection (OBI) is defined by the presence of
HBV DNA in liver and/or serum and negative HBsAg testing. Since
implementation of highly sensitive HBV DNA screening, OBI is also detected
in healthy blood donors. The aims of this study were to investigate
HBV-specific immune responses and genetic variability in donors with OBI,
established by HBV DNA in serum.
METHODS: HBV-specific T-cell responses to HBV antigens were tested in 34
OBI donors by IFN-? ELISpot, cytometric bead array, and intracellular
cytokine staining. As comparison populations, 36 inactive HBV carriers, 22
donors with spontaneously resolved HBV infection, 24 vaccinated donors, and
25 seronegative donors were also included. Surface, pre-S, and pre-c/core
genes from 44 genotype D isolates (24 OBI and 20 HBsAg-positive) were
sequenced.
RESULTS: Immune response of OBI donors to the 3 HBV antigens was 29%-41%,
similar to the response in subjects with resolved HBV infection and higher
than that in HBsAg-positive subjects. On sequence analysis, OBI donors
presented a higher HBsAg mutation rate than HBsAg-positive subjects.
Mutations were clustered in the major hydrophilic region of HBsAg, and no
stop codons or relevant mutations that could affect antigen formation or
detection were observed.
CONCLUSIONS: Our results suggest that immune response can suppress viral
replication to low levels and HBsAg expression to undetectable levels in
OBI blood donors. Relevant mutations were not found in the genomic HBsAg
coding region. Hence, the fact that HBsAg was not detected in OBI is likely
due to low HBsAg production, rather than to a failure of laboratory
reagents. |
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