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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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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).”
From The liver as a central "hub" of the immune system: pathophysiological implications (2025) · cites this paper as [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
- Publisher
- Oxford University Press (OUP)
- 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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