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PMID: 15778368 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Peripheral deletion of antigen-specific T cells leads to long-term tolerance mediated by CD8+ cytotoxic cells.

Journal of immunology (Baltimore, Md. : 1950) ·Vol. 174 ·No. 7 ·2005-04-01 ·Pages 4098-104

Herndon JM, Stuart PM, Ferguson TA

Abstract

Peripheral deletion is one mechanism by which potentially self-reactive clones are removed whether they escape thymic deletion. We have examined the consequences of deleting Ag-specific T cells by i.v. injection of soluble Ag. Deletion of DO11.10 T cells by peptide was mediated predominately via a Fas/FasL mechanism. Animals that underwent deletion were tolerant to subsequent immunization with Ag, even when tolerant mice were given fresh Ag-specific DO11.10 T cells before immunization. Tolerance was mediated by CD8(+) T cells that killed the DO11.10-transgenic T cells in vivo. These data demonstrate that the programmed cell death of large numbers of T cells leads to peripheral tolerance mediated by CD8(+) CTLs.

MeSH Terms
Animals Antigens/administration & dosage,pharmacology Apoptosis/immunology CD8-Positive T-Lymphocytes/immunology,physiology Clonal Deletion/immunology Immune Tolerance Immunization Mice Mice, Inbred BALB C Spleen/cytology T-Cell Antigen Receptor Specificity T-Lymphocytes/cytology,immunology T-Lymphocytes, Cytotoxic/immunology,physiology fas Receptor/physiology
Chemicals
Antigens fas Receptor
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Herndon John M
Department of Ophthalmology and Visual Sciences, Washington University School of Medicine, St. Louis, MO 63110, USA.
Stuart Patrick M
Ferguson Thomas A
Article Info
Journal
Journal of immunology (Baltimore, Md. : 1950)
Abbr.
J Immunol
ISSN
0022-1767
Published
2005-04-01
Pages
4098-104
Language
English
Region
United States
NLM ID
2985117R
Subset
IM
Grants
NEI NIH HHS · EY06765 · United States
NEI NIH HHS · EY08972 · United States
NEI NIH HHS · EY12707 · United States
NEI NIH HHS · EY12826 · United States
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