B cell migration and interactions in the early phase of antibody responses

被引:87
作者
Okada, Takaharu [1 ]
Cyster, Jason G.
机构
[1] Univ Calif San Francisco, Howard Hughes Med Inst, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Microbiol & Immunol, San Francisco, CA 94143 USA
关键词
D O I
10.1016/j.coi.2006.02.005
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In the early phase of thymus-dependent antibody responses antigen-engaged B cells rapidly change their localization within the secondary lymphoid organs to access helper T cells. Central to this process is the tightly controlled distribution of chemokines, sphingosine-1-phosphate and other guidance cues within the lymphoid organ, determined in part by the stromal cells, and the changing responsiveness of activated lymphocytes to these cues. Studies that use the emerging technique of real-time two-photon imaging of intact lymphoid organs began to dissect the dynamics of B cell migration before and after antigen engagement in vivo. Recent studies also provided new insight into antigen transport mechanisms in lymphoid organs and examined signaling requirements for B lymphocyte positioning and motility. Taken together, these studies have provided a more detailed map of the steps involved in B cell migration to encounter antigen and helper T cells early during the adaptive immune response.
引用
收藏
页码:278 / 285
页数:8
相关论文
共 77 条
[1]   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
[2]   In vivo-activated CD4 T cells upregulate CXC chemokine receptor 5 and reprogram their response to lymphoid chemokines [J].
Ansel, KM ;
McHeyzer-Williams, LJ ;
Ngo, VN ;
McHeyzer-Williams, MG ;
Cyster, JG .
JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 190 (08) :1123-1134
[3]   Marginal zone, but not follicular B cells, are potent activators of naive CD4 T cells [J].
Attanavanich, K ;
Kearney, JF .
JOURNAL OF IMMUNOLOGY, 2004, 172 (02) :803-811
[4]   Blood dendritic cells interact with splenic marginal zone B cells to initiate T-Independent immune responses [J].
Balázs, M ;
Martin, F ;
Zhou, T ;
Kearney, JF .
IMMUNITY, 2002, 17 (03) :341-352
[5]   Cell surface recycling of internalized antigen permits dendritic cell priming of B cells [J].
Bergtold, A ;
Desai, DD ;
Gavhane, A ;
Clyne, R .
IMMUNITY, 2005, 23 (05) :503-514
[6]   A member of the dendritic cell family that enters B cell follicles and stimulates primary antibody responses identified by a mannose receptor fusion protein [J].
Berney, C ;
Herren, S ;
Power, CA ;
Gordon, S ;
Martinez-Pomares, L ;
Kosco-Vilbois, MH .
JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 190 (06) :851-860
[7]   B cells and professional APCs recruit regulatory T cells via CCL4 [J].
Bystry, RS ;
Aluvihare, V ;
Welch, KA ;
Kallikourdis, M ;
Betz, AG .
NATURE IMMUNOLOGY, 2001, 2 (12) :1126-1132
[8]   CD4 T cells integrate signals delivered during successive DC encounters in vivo [J].
Celli, S ;
Garcia, Z ;
Bousso, P .
JOURNAL OF EXPERIMENTAL MEDICINE, 2005, 202 (09) :1271-1278
[9]   Sphingosine 1-phosphate receptor 1 promotes B cell localization in the splenic marginal zone [J].
Cinamon, G ;
Matloubian, M ;
Lesneski, MJ ;
Xu, Y ;
Low, C ;
Lu, T ;
Proia, RL ;
Cyster, JG .
NATURE IMMUNOLOGY, 2004, 5 (07) :713-720
[10]  
Cyster JG, 2000, IMMUNOL REV, V176, P181