Integrin Function in T-Cell Homing to Lymphoid and Nonlymphoid Sites: Getting There and Staying There

被引:101
作者
DeNucci, Christopher C. [1 ]
Mitchell, Jason S. [1 ]
Shimizu, Yoji [1 ]
机构
[1] Univ Minnesota, Sch Med, Dept Lab Med & Pathol, Ctr Immunol,Mason Canc Ctr, Minneapolis, MN 55455 USA
关键词
integrin; adhesion; trafficking; retention; lymphocyte; HIGH ENDOTHELIAL VENULES; FUNCTION-ASSOCIATED ANTIGEN-1; ADHESION MOLECULE-1 MADCAM-1; CD103(+) DENDRITIC CELLS; L-SELECTIN; INTRAEPITHELIAL LYMPHOCYTES; EXTRACELLULAR-MATRIX; MONOCLONAL-ANTIBODY; SURFACE-ANTIGEN; MICROENVIRONMENT PROMOTES;
D O I
10.1615/CritRevImmunol.v29.i2.10
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The continuous recirculation of naive T cells and their subsequent migration to tissue following activation is crucial for maintaining protective immunity against invading pathogens. The preferential targeting of effector and memory T cells to tissue is instructed during priming and mediated by cell surface expressed adhesion receptors such as integrins. Integrins are involved in nearly all aspects of T-cell life, including naive T-cell circulation, activation, and finally effector T-cell trafficking and localization. Recent research has revealed that microenvironmental factors present during T-cell priming result in the specific regulation of adhesion/integrin and chemokine receptor expression. Once antigen-experienced T cells enter tissue, further changes in integrin expression may occur that are critical for T-cell localization, retention, effector function, and survival. This review discusses the function of integrin expression on T cells and the multiple roles integrins play on naive T cells and in directing effector T-cell trafficking to nonlymphoid sites in order to maintain protective adaptive immunity at body barriers.
引用
收藏
页码:87 / 109
页数:23
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