Epithelial cells trigger frontline immunoglobulin class switching through a pathway regulated by the inhibitor SLPI

被引:231
作者
Xu, Weifeng
He, Bing
Chiu, April
Chadburn, Amy
Shan, Meimei
Buldys, Malwina
Ding, Aihao
Knowles, Daniel M.
Santini, Paul A.
Cerutti, Andrea [1 ]
机构
[1] Cornell Univ, Weill Med Coll, Dept Pathol & Lab Med, New York, NY 10021 USA
[2] Cornell Univ, Weill Med Coll, Dept Immunol & Microbiol, New York, NY 10021 USA
[3] Cornell Univ, Weill Med Coll, Grad Program Immunol & Microbial Pathogenesis, New York, NY 10021 USA
关键词
D O I
10.1038/ni1434
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Epithelial cells (ECs) transport class-switched immunoglobulin G (IgG) and IgA antibodies across mucous membranes. Whether ECs initiate class switching remains unknown. Here we found that ECs lining tonsillar crypts formed pockets populated by B cells expressing activation-induced cytidine deaminase (AID), an enzyme associated with ongoing class switching. ECs released B cell-activating AID-inducing factors after sensing microbial products through Toll-like receptors. The resulting class switching was amplified by thymic stromal lymphopoietin, an epithelial interleukin 7-like cytokine that enhanced the B cell 'licensing' function of dendritic cells, and was restrained by secretory leukocyte protease inhibitor, an epithelial homeostatic protein that inhibited AID induction in B cells. Thus, ECs may function as mucosal 'guardians' orchestrating frontline IgG and IgA class switching through a Toll-like receptor-inducible signaling program regulated by secretory leukocyte protease inhibitor.
引用
收藏
页码:294 / 303
页数:10
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