Distinct Effects of T-bet in T H 1 Lineage Commitment and IFN-γ Production in CD4 and CD8 T Cells

Author:

Szabo Susanne J.1,Sullivan Brandon M.1,Stemmann Claudia1,Satoskar Abhay R.2,Sleckman Barry P.3,Glimcher Laurie H.14

Affiliation:

1. Department of Immunology and Infectious Diseases, Harvard School of Public Health and

2. Department of Microbiology, Ohio State University, Columbus, OH 43210, USA.

3. Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.

4. Department of Medicine, Harvard Medical School, Boston, MA 02115, USA.

Abstract

T-bet is a member of the T-box family of transcription factors that appears to regulate lineage commitment in CD4 T helper (T H ) lymphocytes in part by activating the hallmark T H 1 cytokine, interferon-γ (IFN-γ). IFN-γ is also produced by natural killer (NK) cells and most prominently by CD8 cytotoxic T cells, and is vital for the control of microbial pathogens. Although T-bet is expressed in all these cell types, it is required for control of IFN-γ production in CD4 and NK cells, but not in CD8 cells. This difference is also apparent in the function of these cell subsets. Thus, the regulation of a single cytokine, IFN-γ, is controlled by distinct transcriptional mechanisms within the T cell lineage.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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