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Cited by 294

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Cytotoxic T lymphocyte responsiveness after resolution of chronic hepatitis B virus infection.

Open access
Rehermann, B, Lau, D, Hoofnagle, J H, Chisari, F V·1996·Journal of Clinical Investigation

Abstract

Clearance of the hepatitis B virus (HBV) during acute hepatitis is associated with a strong, polyclonal, multispecific cytotoxic T lymphocyte (CTL) response to the viral envelope, nucleocapsid and polymerase proteins that persists for decades after clinical recovery. In contrast, chronically infected patients usually fail to mount a strong CTL response to this virus. In this study we demonstrate that chronically infected patients who experience a spontaneous or interferon-induced remission develop a CTL response to HBV that is similar in strength and specificity to patients who have recovered from acute hepatitis. The results suggest that specific immunotherapeutic enhancement of the CTL response to HBV should be possible in chronically infected patients, and that it could lead to viral clearance in these individuals with resolution of chronic liver disease.

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Metadata

Authors
Rehermann, B., Lau, D., Hoofnagle, J. H., & Chisari, F. V.
Venue
Journal of Clinical Investigation
Published
1996-04-01
Volume
97
Issue
7
Pages
1655-1665
ISSN
0021-9738 (ISSN-L)
OpenAlex
W1985262993
Cited by
294
References
0
FWCI
13.67
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Cytotoxic T lymphocyte responsiveness after resolution of chronic hepatitis B virus infection. https://app.cochat.ai/papers/10.1172/jci118592
The paper
Rehermann, B., Lau, D., Hoofnagle, J. H., & Chisari, F. V. (1996). Cytotoxic T lymphocyte responsiveness after resolution of chronic hepatitis B virus infection. Journal of Clinical Investigation. https://doi.org/10.1172/jci118592

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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.