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PMID: 7684435 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

CD28-B7 interactions allow the induction of CD8+ cytotoxic T lymphocytes in the absence of exogenous help.

The Journal of experimental medicine ·Vol. 177 ·No. 6 ·1993-06-01 ·Pages 1791-6

Harding FA, Allison JP

Abstract

The activation requirements for the generation of CD8+ cytotoxic T cells (CTL) are poorly understood. Here we demonstrate that in the absence of exogenous help, a CD28-B7 interaction is necessary and sufficient for generation of class I major histocompatibility complex-specific CTL. Costimulation is required only during the inductive phase of the response, and not during the effector phase. Transfection of the CD28 counter receptor, B7, into nonstimulatory P815 cells confers the ability to elicit P815-specific CTL, and this response can be inhibited by anti-CD28 Fab or by the chimeric B7-binding protein CTLA4Ig. Anti-CD28 monoclonal antibody (mAb) can provide a costimulatory signal to CD8+ T cells when the costimulatory capacity of splenic stimulators is destroyed by chemical fixation. CD28-mediated signaling provokes the release of interleukin 2 (IL-2) from the CD8+ CTL precursors, as anti-CD28 mAb could be substituted for by the addition of IL-2, and an anti-IL-2 mAb can block the generation of anti-CD28-induced CTL. CD4+ cells are not involved in the costimulatory response in the systems examined. We conclude that CD8+ T cell activation requires two signals: an antigen-specific signal mediated by the T cell receptor, and an additional antigen nonspecific signal provided via a CD28-B7 interaction.

MeSH Terms
Animals Antigens, CD/immunology Antigens, Differentiation, T-Lymphocyte/immunology Antigens, Surface/immunology B7-1 Antigen CD28 Antigens CD4-Positive T-Lymphocytes/immunology CD8 Antigens/immunology Cell Line Cells, Cultured Cytotoxicity, Immunologic Interleukin-2/pharmacology Lymphocyte Activation Mice Mice, Inbred C3H Mice, Inbred C57BL T-Lymphocytes, Cytotoxic/immunology
Chemicals
Antigens, CD Antigens, Differentiation, T-Lymphocyte Antigens, Surface B7-1 Antigen CD28 Antigens CD8 Antigens Interleukin-2
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Harding F A
Department of Molecular and Cell Biology, University of California, Berkeley 94720.
Allison J P
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Article Info
Journal
The Journal of experimental medicine
Abbr.
J Exp Med
ISSN
0022-1007
Published
1993-06-01
Pages
1791-6
Language
English
Region
United States
NLM ID
2985109R
PMCID
PMC2191062
Subset
IM
Grants
NCI NIH HHS · CA-40041 · United States
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