CXCL13 is required for B1 cell homing, natural antibody production, and body cavity immunity

被引:412
作者
Ansel, KM
Harris, RBS
Cyster, JG
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
[3] Univ Georgia, Dept Foods & Nutr, Athens, GA 30602 USA
关键词
D O I
10.1016/S1074-7613(01)00257-6
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
B1 cells are a predominant cell type in body cavities and an important source of natural antibody. Here we report that in mice lacking the chemokine, CXCL13, B1 cells are deficient in peritoneal and pleural cavities but not in spleen. CXCL13 is produced by cells in the omentum and by peritoneal macrophages, and in adoptive transfers, B1 cells home to the omentum and the peritoneal cavity in a CXCL13-dependent manner. CXCL13(-/-) mice are deficient in preexisting phosphorylcholine (PC)-specific antibodies and in their ability to mount an anti-PC response to peritoneal streptococcal antigen. These findings provide insight into the mechanism of B1 cell homing and establish a critical role for B1 cell compartmentalization in the production of natural antibodies and for body cavity immunity.
引用
收藏
页码:67 / 76
页数:10
相关论文
共 44 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]   Chemokines in lymphopoiesis and lymphoid organ development [J].
Ansel, KM ;
Cyster, JG .
CURRENT OPINION IN IMMUNOLOGY, 2001, 13 (02) :172-179
[3]   NATURAL AUTOANTIBODIES - THE OTHER SIDE OF THE IMMUNE-SYSTEM [J].
AVRAMEAS, S ;
TERNYNCK, T .
RESEARCH IN IMMUNOLOGY, 1995, 146 (4-5) :235-248
[4]   B-1 and B-2 cell-derived immunoglobulin M antibodies are nonredundant components of the protective response to influenza virus infection [J].
Baumgarth, N ;
Herman, OC ;
Jager, GC ;
Brown, LE ;
Herzenberg, LA ;
Chen, JZ .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (02) :271-280
[5]  
BEELEN RHJ, 1980, J RETICULOENDOTH SOC, V28, P601
[6]   Increased junctional diversity in fetal B cells results in a loss of protective anti-phosphorylcholine antibodies in adult mice [J].
Benedict, CL ;
Kearney, JF .
IMMUNITY, 1999, 10 (05) :607-617
[7]   A critical role of natural immunoglobulin M in immediate defense against systemic bacterial infection [J].
Boes, M ;
Prodeus, AP ;
Schmidt, T ;
Carroll, MC ;
Chen, JZ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (12) :2381-2386
[8]   Developmental switches in chemokine response profiles during B cell differentiation and maturation [J].
Bowman, EP ;
Campbell, JJ ;
Soler, D ;
Dong, ZJ ;
Manlongat, N ;
Picarella, D ;
Hardy, RR ;
Butcher, EC .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 191 (08) :1303-1317
[9]   ANTI-PHOSPHOCHOLINE ANTIBODIES FOUND IN NORMAL MOUSE SERUM ARE PROTECTIVE AGAINST INTRAVENOUS INFECTION WITH TYPE-3 STREPTOCOCCUS-PNEUMONIAE [J].
BRILES, DE ;
NAHM, M ;
SCHROER, K ;
DAVIE, J ;
BAKER, P ;
KEARNEY, J ;
BARLETTA, R .
JOURNAL OF EXPERIMENTAL MEDICINE, 1981, 153 (03) :694-705
[10]   A VH11Vκ9B cell antigen receptor drives generation of CD5+ B cells both in vivo and in vitro [J].
Chumley, MJ ;
Dal Porto, JM ;
Kawaguchi, S ;
Cambier, JC ;
Nemazee, D ;
Hardy, RR .
JOURNAL OF IMMUNOLOGY, 2000, 164 (09) :4586-4593