4.1 Review

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

Journal

CRITICAL REVIEWS IN IMMUNOLOGY
Volume 29, Issue 2, Pages 87-109

Publisher

BEGELL HOUSE INC
DOI: 10.1615/CritRevImmunol.v29.i2.10

Keywords

integrin; adhesion; trafficking; retention; lymphocyte

Categories

Funding

  1. NIH [AI031126, AI038474, AI064271, F30 DK082139, T32 CA009138]
  2. Harry Kay Chair in Biomedical Research
  3. NATIONAL CANCER INSTITUTE [T32CA009138] Funding Source: NIH RePORTER
  4. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [R01AI064271, R01AI038474, R56AI038474, R29AI031126, R01AI031126] Funding Source: NIH RePORTER
  5. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [F30DK082139] Funding Source: NIH RePORTER

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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.

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