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PMID: 7895163 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

The liver eliminates T cells undergoing antigen-triggered apoptosis in vivo.

Immunity ·Vol. 1 ·No. 9 ·1994-12-00 ·Pages 741-9

Huang L, Soldevila G, Leeker M, Flavell R, Crispe IN

Abstract

Deletion of mature peripheral T cells may result from TCR ligation by bacterial enterotoxins, endogenous provirus-encoded superantigens, and peptide antigens. But the ultimate fate of deleted T cells is not clear. Using a line of T cell receptor transgenic mice injected with antigenic peptide, we have documented that peripheral deletion is accompanied by the induction of abortive T cell activation followed by the disappearance of transgene-positive T cells. As these T cells disappear from the lymph nodes and spleen, they accumulate in the liver, where they undergo apoptosis. This is likely to be a general clearance pathway for T cells that are programmed to undergo apoptosis in vivo, and it may further explain the expansion of the intrahepatic T cell pool in mice with genetic defects in the T cell apoptosis mechanism, such as the lpr mutant.

MeSH Terms
Animals Antigens, Polyomavirus Transforming/immunology Apoptosis/immunology Immunization Liver/immunology,pathology Lymphocyte Activation Mice Mice, Transgenic Polyomavirus/immunology Receptors, Antigen, T-Cell/genetics,immunology Spleen/immunology,pathology T-Lymphocytes/immunology,pathology
Chemicals
Antigens, Polyomavirus Transforming Receptors, Antigen, T-Cell
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Huang L
Section of Immunobiology, Yale University School of Medicine, New Haven, Connecticut 06510.
Soldevila G
Leeker M
Flavell R
Crispe I N
Article Info
Journal
Immunity
Abbr.
Immunity
ISSN
1074-7613
Published
1994-12-00
Pages
741-9
Language
English
Region
United States
NLM ID
9432918
Subset
IM
Grants
NIAID NIH HHS · AI 30561 · United States
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