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
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
收藏
页码:117 / 135
页数:19
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共 142 条
[1]   Three distinctive steps in Peyer's patch formation of murine embryo [J].
Adachi, S ;
Yoshida, H ;
Kataoka, H ;
Nishikawa, S .
INTERNATIONAL IMMUNOLOGY, 1997, 9 (04) :507-514
[2]   Essential role of IL-7 receptor α in the formation of Peyer's patch anlage [J].
Adachi, S ;
Yoshida, H ;
Honda, K ;
Maki, K ;
Saijo, K ;
Ikuta, K ;
Saito, T ;
Nishikawa, S .
INTERNATIONAL IMMUNOLOGY, 1998, 10 (01) :1-6
[3]   Abnormal development of secondary lymphoid tissues in lymphotoxin beta-deficient mice [J].
Alimzhanov, MB ;
Kuprash, DV ;
KoscoVilbois, MH ;
Luz, A ;
Turetskaya, RL ;
Tarakhovsky, A ;
Rajewsky, K ;
Nedospasov, SA ;
Pfeffer, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (17) :9302-9307
[4]   A chemokine-driven positive feedback loop organizes lymphoid follicles [J].
Ansel, KM ;
Ngo, VN ;
Hyman, PL ;
Luther, SA ;
Förster, R ;
Sedgwick, JD ;
Browning, JL ;
Lipp, M ;
Cyster, JG .
NATURE, 2000, 406 (6793) :309-314
[5]   The CCR7 ligand ELC (CCL19) is transcytosed in high endothelial venules and mediates T cell recruitment [J].
Baekkevold, ES ;
Yamanaka, T ;
Palframan, RT ;
Carlsen, HS ;
Reinholt, FP ;
von Andrian, UH ;
Brandtzaeg, P ;
Haraldsen, G .
JOURNAL OF EXPERIMENTAL MEDICINE, 2001, 193 (09) :1105-1111
[6]  
BANKS TA, 1995, J IMMUNOL, V155, P1685
[7]   EPSTEIN-BARR VIRUS-INDUCED GENES - 1ST LYMPHOCYTE-SPECIFIC G-PROTEIN-COUPLED PEPTIDE RECEPTORS [J].
BIRKENBACH, M ;
JOSEFSEN, K ;
YALAMANCHILI, R ;
LENOIR, G ;
KIEFF, E .
JOURNAL OF VIROLOGY, 1993, 67 (04) :2209-2220
[8]   Follicular B helper T cells express CXC chemokine receptor 5, localize to B cell follicles, and support immunoglobulin production [J].
Breitfeld, D ;
Ohl, L ;
Kremmer, E ;
Ellwart, J ;
Sallusto, F ;
Lipp, M ;
Förster, R .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (11) :1545-1551
[9]   EXPRESSION OF THE CHEMOKINE RECEPTOR BLR2/EBI1 IS SPECIFICALLY TRANSACTIVATED BY EPSTEIN-BARR-VIRUS NUCLEAR ANTIGEN-2 [J].
BURGSTAHLER, R ;
KEMPKES, B ;
STEUBE, K ;
LIPP, M .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1995, 215 (02) :737-743
[10]   Lymphocyte homing and homeostasis [J].
Butcher, EC ;
Picker, LJ .
SCIENCE, 1996, 272 (5258) :60-66