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PMID: 2783992 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Does T-cell tolerance require a dedicated antigen-presenting cell?

Nature ·Vol. 338 ·No. 6210 ·1989-03-02 ·Pages 74-6

Matzinger P, Guerder S

Abstract

Almost 30 years ago Burnet proposed that the immune system maintained self-tolerance by deleting autoreactive lymphocytes. Recently it has become clear that for T cells this step occurs in the thymus, where developing T cells first express their antigen-specific receptors. Here a T-cell which encounters its antigen disappears--if it is not dead, it at least stops expressing its receptors. In the periphery by contrast, encounter with antigen leads to activation and proliferation of the responding T-cell. There are two possible explanations for this difference. Either the antigen-presenting cells in the thymus are different from those in the periphery and instead of producing positive signals they directly or indirectly kill the thymocytes; or the T cells themselves are different, and like immature B cells, may die after encounter with antigen. We tested the first possibility and found that dendritic cells from spleen, which are the most potent activators of mature T cells, are also the most potent inactivators of young developing T cells. Thus it is not the antigen-presenting cell which determines whether a T-cell responds or dies, but the T-cell itself or its thymic environment.

MeSH Terms
Animals Antigen-Presenting Cells/immunology Fetus Immune Tolerance Mice Mice, Inbred Strains Organ Culture Techniques T-Lymphocytes/cytology,immunology,radiation effects Thymus Gland/immunology
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Matzinger P
Basel Institute for Immunology, Switzerland.
Guerder S
Article Info
Journal
Nature
Abbr.
Nature
ISSN
0028-0836
Published
1989-03-02
Pages
74-6
Language
English
Region
England
NLM ID
0410462
Subset
IM
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