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      Cytokine-induced differentiation of precursor mouse CD8+ T cells into cytotoxic CD8+ T cells secreting Th1 or Th2 cytokines.

      Immunity
      Animals, B-Lymphocytes, immunology, Cell Differentiation, Cell Line, Cytotoxicity Tests, Immunologic, Female, Flow Cytometry, Immunoglobulin Isotypes, Interleukin-4, physiology, Interleukins, biosynthesis, secretion, Lymphocyte Cooperation, Mice, Mice, Inbred BALB C, Mice, Inbred C57BL, Mice, Inbred CBA, T-Lymphocytes, Cytotoxic, Th1 Cells, Th2 Cells

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          Abstract

          Alloantigen-stimulated CD8+ mouse spleen cells, either spontaneously or in the presence of IL-12 or IFN gamma plus anti-IL-4, differentiate into CD8+ T cells secreting a Th1-like cytokine pattern (IL-2 and IFN gamma). IL-4 induced differentiation into CD8+ T cells secreting Th2 cytokines (IL-4, IL-5, IL-6, and IL-10), whereas anti-IFN gamma suppressed the development of CD8+ cells secreting IFN gamma. Clones of IL-4- or IFN gamma-producing CD8+ T cells were relatively stable, as IL-4 or IFN gamma did not cause interconversion of committed CD8+ T cells. Both CD8+ subsets were cytotoxic, failed to provide cognate help for B cell antibody production, and remained CD4-, CD8 alpha+ CD8 beta+. We propose the names TC1 and TC2 for cytotoxic CD8+ T cells secreting Th1-like and Th2-like cytokines, respectively.

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