4.7 Article

Immune evasion versus recovery after acute hepatitis C virus infection from a shared source

Journal

JOURNAL OF EXPERIMENTAL MEDICINE
Volume 201, Issue 11, Pages 1725-1731

Publisher

ROCKEFELLER UNIV PRESS
DOI: 10.1084/jem.20042284

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Funding

  1. NIDDK NIH HHS [DK60345, R01 DK060590, U01 DK060345] Funding Source: Medline

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Acute infection with hepatitis C virus (HCV) rarely is identified, and hence, the determinants of spontaneous resolution versus chronicity remain incompletely understood. In particular, because of the retrospective nature and unknown source of infection in most human studies, direct evidence for emergence of escape mutations in immunodominant major histocompatibility complex class I-restricted epitopes leading to immune evasion is extremely limited. In two patients infected accidentally with an identical HCV strain but who developed divergent outcomes, the total lack of HCV- specific CD4(+) T cells in conjunction with vigorous CD8(+) T cells that targeted a single epitope in one patient was associated with mutational escape and viral persistence. Statistical evidence for positive Darwinian selective pressure against an immunodominant epitope is presented. Wild-type cytotoxic T lymphocytes persisted even after the cognate antigen was no longer present.

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