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PMID: 11825566 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

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

Immunity ·Vol. 16 ·No. 1 ·2002-01-00 ·Pages 67-76

Ansel KM, Harris RB, Cyster JG

Abstract

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.

MeSH Terms
Animals Antibody Formation B-Lymphocytes/physiology Cell Movement Chemokine CXCL13 Chemokines, CXC/genetics,physiology Chemotaxis Lymphocyte Count Male Mice Mice, Inbred C57BL Omentum/cytology,immunology Parabiosis Peritoneal Cavity/cytology RNA, Messenger/analysis
Chemicals
Chemokine CXCL13 Chemokines, CXC Cxcl13 protein, mouse RNA, Messenger
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Ansel K Mark
Howard Hughes Medical Institute and Department of Microbiology and Immunology, University of California, San Francisco, 513 Parnassus Avenue, San Francisco, CA 94143, USA.
Harris Ruth B S
Cyster Jason G
Article Info
Journal
Immunity
Abbr.
Immunity
ISSN
1074-7613
Published
2002-01-00
Pages
67-76
Language
English
Region
United States
NLM ID
9432918
Subset
IM
Grants
NIAID NIH HHS · AI45073 · United States
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