Cited by 201T-cell and B-cell ImmunologyHepatitis B Virus StudiesImmunotherapy and Immune Responses

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Class I-restricted cytotoxic T lymphocytes are directly cytopathic for their target cells in vivo.

Abstract

Although CD8-positive, class I-restricted CTL play a critical role in viral clearance and immunopathology in many model systems, they have not been shown to directly kill their target cells in vivo at the single cell level. Using a hepatitis B surface Ag transgenic mouse model of class I-restricted, CTL-mediated liver disease, we now demonstrate that CD8-positive, Ld-restricted hepatitis B surface Ag-specific CTL bind and kill their target cells in vivo by triggering them to undergo degenerative cytologic changes compatible with apoptosis. Unexpectedly, the data also indicate that the pathologic consequences of this direct, Ag-specific CTL effect are much less severe than the cytodestructive, Ag-nonspecific inflammatory response that they induce when they are activated by Ag recognition.

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Crossref · 10.4049/jimmunol.152.7.3245

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  • Early work showed how effector CD8+ T cells specific for HBV envelope, when adoptively transferred in HBV transgenic mice, were sequestered and activated selectively in the liver, despite expression of antigen also in renal tubular epithelium and choroid plexus.

    “Early work showed how effector CD8+ T cells specific for hepatitis 455 B virus (HBV) envelope, when adoptively transferred in HBV transgenic mice, were 456 sequestered and activated selectively in the liver, despite the expression of antigen also in 457 the renal tubular epithelium and choroid plexus(92).”

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Cited by 201

Metadata

Authors
Ando, K., Guidotti, L. G., Wirth, S., Ishikawa, T., Missale, G., Moriyama, T., Schreiber, R. D., Schlicht, H. J., Huang, S. N., & Chisari, F. V.
Affiliations
Scripps Research Institute (US)
Venue
The Journal of Immunology
Published
1994-04-01
Volume
152
Issue
7
Pages
3245-3253
ISSN
  • 0022-1767 (ISSN-L)
  • 1550-6606
OpenAlex
W1565398120
Cited by
201
References
0
Citations by year
2026: 2 · 2025: 1 · 2024: 3 · 2023: 2 · 2022: 2 · 2021: 1 · 2020: 2 · 2018: 2 · 2016: 4 · 2015: 11 · 2014: 5 · 2013: 7 · 2012: 9
FWCI
5.30
Type
journal article
Language
en
Open access
closed
Locations
  • The Journal of Immunology (publishedVersion)
  • PubMed (publishedVersion)
Funders
National Cancer Institute (CA40489, CA-54560, R01CA054560)
Topics
  • Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
  • Health Sciences › Medicine › Epidemiology › Hepatitis B Virus Studies
  • Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
Keywords
CD8+ T cells, hepatitis B surface antigen, liver disease, apoptosis, immunopathology, viral clearance
MeSH terms
Animals, Cytotoxicity, Immunologic, DNA Damage, H-2 Antigens, Hepatitis B Surface Antigens, Immunization, Passive, Liver Diseases, Mice, Transgenic, T-Lymphocytes, Cytotoxic, Apoptosis, Mice

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