CD80 expression on B cells regulates murine T follicular helper development, germinal center B cell survival, and plasma cell generation.

CD80 expression on B cells regulates murine T follicular helper development, germinal center B cell survival, and plasma cell generation.
复制标题

DOI:
10.4049/jimmunol.1102885
复制
发表时间:
2012-05-01
期刊:
Journal of immunology (Baltimore, Md. : 1950)
影响因子:
--
通讯作者:
Shlomchik MJ
Shlomchik MJ
中科院分区:
其他
文献类型:
--
作者:
Good-Jacobson KL;Song E;Anderson S;Sharpe AH;Shlomchik MJ

文献摘要

参考文献

被引文献

相似文献

尽管调节这些长寿群体形成的机制尚不清楚,但在高亲和力长寿浆细胞(PC)和记忆B细胞的产生中,生殖中心(GC)B细胞和T滤泡辅助(TFH)细胞相互作用。由于CD 80是人类和小鼠记忆B细胞共有的少数标志物之一,我们研究了其在GC、记忆细胞和PC发育中的作用。在CD 80缺陷小鼠中,与B6对照相比,免疫后产生的长寿命PC较少。一致地,在GC收缩期,CD 80的缺乏导致凋亡的GC B细胞增加。与B6相比,CD 80 −/−小鼠的TFH较少,残留的TFH细胞未能成熟,ICOS和PD-1表达减少,IL-21 mRNA合成减少。混合骨髓嵌合体表现出B细胞对正常TFH和PC发育的CD 80表达的内在要求。因此,B细胞表达CD 80在调节早期和晚期GC反应中的B-T相互作用中起关键作用。这反过来又导致生产长寿命PC的能力受损。这些数据为GC和AFC的发育以及CD 80在体液免疫中的功能提供了新的见解。
Germinal center (GC) B cells and T follicular helper (TFH) cells interact in the production of high-affinity long-lived plasma cells (PCs) and memory B cells, though the mechanisms regulating the formation of these long-lived populations remain unclear. Because CD80 is one of the few markers shared by human and murine memory B cells, we investigated its role in the development of GCs, memory cells and PCs. In CD80-deficient mice, fewer long-lived PCs were generated upon immunization, compared to B6 controls. In concert, the absence of CD80 resulted in an increase in apoptotic GC B cells during the contraction phase of the GC. CD80−/− mice had fewer TFH compared to B6, and residual TFH cells failed to mature, with decreased ICOS and PD-1 expression and decreased synthesis of IL-21 mRNA. Mixed bone marrow chimeras demonstrated a B cell-intrinsic requirement for CD80 expression for normal TFH and PC development. Therefore, B cell expression of CD80 plays a critical role in regulating B-T interactions in both early and late GC responses. This, in turn, results in impaired ability to produce long-lived PCs. These data provide new insights into the development of GCs and AFCs and the functions of CD80 in humoral immunity.
DOI: 10.1093/intimm/5.6.647
发表时间: 1993-06-01
影响因子: 4.4
作者:
CHEN, JZ;TROUNSTINE, M;HUSZAR, D
通讯作者: HUSZAR, D
DOI: 10.1126/science.1136736
发表时间: 2007-01-26
期刊: SCIENCE
影响因子: 56.9
作者:
Allen, Christopher D. C.;Okada, Takaharu;Cyster, Jason G.
通讯作者: Cyster, Jason G.
DOI: 10.1016/j.immuni.2011.03.023
发表时间: 2011-06-24
期刊: Immunity
影响因子: 32.4
作者:
Choi YS;Kageyama R;Eto D;Escobar TC;Johnston RJ;Monticelli L;Lao C;Crotty S
通讯作者: Crotty S
DOI: 10.1084/jem.20062571
发表时间: 2007-09-03
期刊: The Journal of experimental medicine
影响因子: --
作者:
Anderson SM;Tomayko MM;Ahuja A;Haberman AM;Shlomchik MJ
通讯作者: Shlomchik MJ
DOI: 10.1038/ni.1814
发表时间: 2009-12-01
期刊: NATURE IMMUNOLOGY
影响因子: 30.5
作者:
Dogan, Ismail;Bertocci, Barbara;Weill, Jean-Claude
通讯作者: Weill, Jean-Claude