Role of NK1.1 <sup>+</sup> T Cells in a T <sub>H</sub> 2 Response and in Immunoglobulin E Production

Tomohiro Yoshimoto(National Institute of Allergy and Infectious Diseases), Albert Bendelac(Princeton University), L. Cynthia Watson(National Institute of Allergy and Infectious Diseases), Jane Hu‐Li(National Institute of Allergy and Infectious Diseases), William E. Paul(National Institute of Allergy and Infectious Diseases)
Science
December 15, 1995
Cited by 497

Abstract

Immune responses dominated by interleukin-4 (IL-4)-producing T helper type 2 (TH2) cells or by interferon gamma (IFN-gamma)-producing T helper type 1 (TH1) cells express distinctive protection against infection with different pathogens. Interleukin-4 promotes the differentiation of naïve CD4+ T cells into IL-4 producers and suppresses their development into IFN-gamma producers. CD1-specific splenic CD4+NK1.1+ T cells, a numerically minor population, produced IL-4 promptly on in vivo stimulation. This T cell population was essential for the induction of IL-4-producing cells and for switching to immunoglobulin E, an IL-4-dependent event, in response to injection of antibodies to immunoglobulin D.


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