Mechanisms Underlying Lineage Commitment and Plasticity of Helper CD4 + T Cells

Author:

O’Shea John J.1,Paul William E.1

Affiliation:

1. Molecular Immunology and Inflammation Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, Laboratory of Immunology, National Institute of Allergy and Infectious Disease, National Institutes of Health, Bethesda, MD 20892–1616, USA.

Abstract

Critical Mediators Helper T cells are the immune system's ringmasters, having a multiplicity of functions that mediate the body's immune responses to infections. Depending on the type of infection, CD4 + helper T cells respond by secreting specific patterns of cytokines, which provide important cues to other subsets of immune cells. CD4 + T cells with distinct cytokine profiles have been viewed classically as separate lineages; however, there is mounting evidence that these cells may not be terminally differentiated but are in fact quite plastic. O'Shea and Paul (p. 1098 ) review the current understanding of CD4 + T cell subset differentiation and the underlying mechanisms that drive cell-lineage commitment.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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