Local increase in thymic stromal lymphopoietin induces systemic alterations in B cell development

被引:83
作者
Astrakhan, Alexander
Omori, Miyuki
Nguyen, Thuc
Becker-Herman, Shirly
Iseki, Masanori
Aye, Theingi
Hudkins, Kelly
Dooley, James
Farr, Andrew
Alpers, Charles E.
Ziegler, Steven F.
Rawlings, David J. [1 ]
机构
[1] Univ Washington, Sch Med, Dept Immunol, Seattle, WA 98195 USA
[2] Benaroya Res Inst, Seattle, WA 98195 USA
[3] Univ Washington, Sch Med, Dept Med, Seattle, WA 98195 USA
[4] Univ Washington, Sch Med, Dept Pediat, Seattle, WA 98195 USA
[5] Univ Washington, Sch Med, Dept Pathol, Seattle, WA 98195 USA
[6] Univ Washington, Sch Med, Dept Biol Struct, Seattle, WA 98195 USA
关键词
D O I
10.1038/ni1452
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 cytokine thymic stromal lymphopoietin ( TSLP) drives immature B cell development in vitro and may regulate T helper type 2 responses. Here we analyzed the involvement of TSLP in B cell development in vivo with a doxycycline-inducible, keratin 5 driven transgene encoding TSLP (K5-TSLP). K5-TSLP-transgenic mice given doxycycline showed an influx of immature B cells into the periphery, with population expansion of follicular mature B cells, near-complete loss of marginal zone and marginal zone precursor B cells, and 'preferential' population expansion of peritoneal B-1b B cells. These changes promoted cryoglobulin production and immune complex-mediated renal disease. Identical events occurred in mice without T cells, in alternative TSLP-transgenic models and in K5-TSLP-transgenic mice with undetectable systemic TSLP. These observations suggest that signals mediating localized TSLP expression may modulate systemic B cell development and promote humoral autoimmunity.
引用
收藏
页码:522 / 531
页数:10
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