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CD8 <sup>+</sup> T Cells Mediate Viral Clearance and Disease Pathogenesis during Acute Hepatitis B Virus Infection
Journal of Virology · 2002 · Vol. 77(1) · pp. 68–76
Robert Thimme(Scripps Research Institute)Stefan Wieland(Scripps Research Institute)Carola Steiger(Scripps Research Institute)John GhrayebKeith A. Reimann(Beth Israel Deaconess Medical Center)Robert H. Purcell(National Institutes of Health)Francis V. Chisari✉(Scripps Research Institute)
Abstract
Although the CD4(+)- and CD8(+)-T-cell responses to the hepatitis B virus (HBV) are thought to be crucial for the control of HBV infection, the relative contribution of each T-cell subset as an effector of viral clearance is not known. To examine this question, we monitored the course of HBV infection in control, CD4-depleted, and CD8-depleted chimpanzees. Our results demonstrate that CD8(+) cells are the main effector cells responsible for viral clearance and disease pathogenesis during acute HBV infection, and they suggest that viral clearance is mediated by both noncytolytic and cytolytic effector functions of the CD8(+)-T-cell response.
Hepatitis B Virus StudiesHIV Research and TreatmentImmune Cell Function and InteractionBiologyEffectorPathogenesisVirologyHepatitis B virusCD8CytolysisViral pathogenesisVirusCytotoxic T cell
MeSH terms
Acute DiseaseAnimalsPan troglodytesHepatitis BInterferon-gammaCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesViral Load
Funding
- Cancer Research Institute
- Deutsche Forschungsgemeinschaft
- National Institutes of Health
Citations
966
FWCI
13.95
field-weighted impact
References
37
Percentile
99%
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Citations per year
Cited by
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References
Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction
Analytical Biochemistry · 1987 · 63,248 citations
CD4+ T cells are required to sustain CD8+ cytotoxic T-cell responses during chronic viral infection
Journal of Virology · 1994 · 1,145 citations
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