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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