Antigen-dependent clonal expansion of a trace population of antigen- specific CD4+ T cells in vivo is dependent on CD28 costimulation and inhibited by CTLA-4

Elizabeth R. Kearney, Theresa L. Walunas, Robert W. Karr, Phillip A. Morton, Dennis Y. Loh, Jeffrey A. Bluestone, Marc Jenkins

Research output: Contribution to journalArticlepeer-review

288 Scopus citations

Abstract

The importance of CD28 costimulation to a primary T cell response in vivo was assessed in an adoptive transfer system where a small population of peptide-specific CD4+ TCR transgenic T cells can be physically tracked. Ag- dependent clonal expansion of the transgenic T cells in draining lymph nodes was blocked by cyclosporin A and required a CD28 signal that was completely inhibited by CTLA-4-Ig or a combination of anti-B7-1 and anti-B7-2 mAbs, but not by either Ab alone. In vivo treatment with the combination of anti-B7-1 and anti-B7-2 mAbs also blocked conversion of the Ag-specific T cells to the activated phenotype. In contrast, anti-CTLA-4 Fab greatly enhanced the in vivo clonal expansion of the Ag-specific T cells. These results suggest that Ag-driven proliferation and phenotype conversion of naive CD4+ T cells is dependent on CD28-derived signals and is inhibited by CTLA-4.

Original languageEnglish (US)
Pages (from-to)1032-1036
Number of pages5
JournalJournal of Immunology
Volume155
Issue number3
StatePublished - 1995

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