Chemokine-Driven CD4+ T Cell Homing: New Concepts and Recent Advances

被引:18
作者
Gregor, Carly E. [1 ]
Foeng, Jade [1 ]
Comerford, Iain [1 ]
McColl, Shaun R. [1 ]
机构
[1] Univ Adelaide, Chemokine Biol Lab, Sch Biol Sci, Adelaide, SA, Australia
来源
ADVANCES IN IMMUNOLOGY, VOL 135 | 2017年 / 135卷
关键词
EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; FIBROBLASTIC RETICULAR CELLS; GROWTH-FACTOR-BETA; PERIPHERAL LYMPHOID ORGANS; HIGH ENDOTHELIAL VENULES; FOLLICULAR HELPER-CELLS; EOTAXIN RECEPTOR CCR3; SPLENIC WHITE PULP; IN-VIVO FUNCTION; TRANSCRIPTION-FACTOR;
D O I
10.1016/bs.ai.2017.03.001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
CD4(+) T cells are critical regulators of the adaptive immune system and have diverse roles in regulating responses to the broad array of microbes encountered. Appropriate execution of their effector function requires precise and coordinatedmigration of these cells to specific lymphoid niches and peripheral sites. This migration is largely controlled by dynamic expression of chemokine receptors and the discrete functions of distinct subsets of CD4(+) T cells can often be determined from their expression of specific chemokine receptors. In this chapter, we discuss recent advances in the subset-specific homing of distinct T helper populations, focusing on new insights stemming from the increased diversity and plasticity now observed among CD4(+) T cells as well as how chemokine receptors can govern T cell-fate decisions. We also discuss current understanding of CD4(+) memory T cells with reference to their diversification based on chemokine receptor expression.
引用
收藏
页码:119 / 181
页数:63
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