γδ T Cells: First Line of Defense and Beyond

Author:

Chien Yueh-hsiu12,Meyer Christina2,Bonneville Marc3

Affiliation:

1. Department of Microbiology and Immunology and

2. Program of Immunology, Stanford University, Stanford, California 94305;,

3. Institut National de la Santé et de la Recherche Médicale (INSERM) U892, IRT UN, 44007 Nantes Cedex 1, France;

Abstract

γδ T cells, αβ T cells, and B cells are present together in all but the most primitive vertebrates, suggesting that each population contributes to host immune competence uniquely and that all three are necessary for maintaining immune competence. Functional and molecular analyses indicate that in infections, γδ T cells respond earlier than αβ T cells do and that they emerge late after pathogen numbers start to decline. Thus, these cells may be involved in both establishing and regulating the inflammatory response. Moreover, γδ T cells and αβ T cells are clearly distinct in their antigen recognition and activation requirements as well as in the development of their antigen-specific repertoire and effector function. These aspects allow γδ T cells to occupy unique temporal and functional niches in host immune defense. We review these and other advances in γδ T cell biology in the context of their being the major initial IL-17 producers in acute infection.

Publisher

Annual Reviews

Subject

Immunology,Immunology and Allergy

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