The impact of CCR7 and CXCR5 on lymphoid organ development and systemic immunity

被引：204

作者：

Müller, G ^{[1
]}

Höpken, UE ^{[1
]}

Lipp, M ^{[1
]}

机构：

[1] Max Delbruck Ctr Mol Med, Dept Mol Tumor Genet & Immunogenet, D-13092 Berlin, Germany

来源：

IMMUNOLOGICAL REVIEWS | 2003年 / 195卷

关键词：

D O I：

10.1034/j.1600-065X.2003.00073.x

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 development of secondary lymphoid organs is a complex process dependent on a coordinated interaction of cells of hematopoietic and non-hematopoietic origin. In this context, chemokines and cytokines belonging to the tumor necrosis factor (TNF)/lymphotoxin (LT) family are critical signaling molecules during the initial steps of lymph node and Peyer's patch organogenesis. Homeostatic chemokines, such as CXCL13, CCL21, and CCL19, as well as their corresponding receptors, CXCR5 and CCR7, have now been shown to closely cooperate in the development of lymphoid organs and the maintenance of lymphoid tissue microarchitecture. We summarize recent data on the function of CXCR5 and CCR7 and their intricate connection to the TNF/LT system in order to refine the current model of lymphoid organ development.

引用

页码：117 / 135

页数：19

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