Inflammatory cytokines provide a third signal for activation of naive CD4+ and CD8+ T cells

Julie M. Curtsinger, Clint S. Schmidt, Anna Mondino, Debra C. Lins, Ross M. Kedl, Marc K. Jenkins, Matthew F. Mescher

Research output: Contribution to journalArticlepeer-review

Abstract

The effects of inflammatory cytokines on naive T cells have been studied using MHC protein/peptide complexes on microspheres, thus avoiding the use of APCs whose functions may be affected by the cytokines. IL-1, but not IL-12, increased proliferation of CD4+ T cells in response to Ag and IL-2, which is consistent with effects on in vivo priming of CD4+ cells. In contrast, proliferation of CD8+ T cells to Ag and IL-2 required IL-12, and IL-12 replaced adjuvant in stimulating an in vivo response to peptide. These results support a model in which distinct inflammatory cytokines act directly on naive CD4+ and CD8+ T cells to provide a third signal, along with Ag and IL-2, to optimally activate differentiation and clonal expansion.

Original languageEnglish
Pages (from-to)3256-3262
Number of pages7
JournalJournal of Immunology
Volume162
Issue number6
Publication statusPublished - Mar 15 1999

ASJC Scopus subject areas

  • Immunology

Fingerprint Dive into the research topics of 'Inflammatory cytokines provide a third signal for activation of naive CD4+ and CD8+ T cells'. Together they form a unique fingerprint.

Cite this