CARD11 signaling in regulatory T cell development and function.

CARD11 signaling in regulatory T cell development and function.
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DOI:
10.1016/j.jbior.2022.100890
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发表时间:
2022-05
影响因子:
--
通讯作者:
Pomerantz, Joel L.
Pomerantz, Joel L.
中科院分区:
其他
文献类型:
--
作者:
Carter, Nicole M.;Pomerantz, Joel L.

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调节性T细胞(Tcells)是调节免疫应答以防止自身免疫和慢性炎症的CD 4 T细胞的关键子集。CARD 11是一种信号枢纽和支架蛋白,将抗原受体接合与NF-κB和其他下游信号通路的激活联系起来,对于胸腺Treg的发育和功能至关重要。缺乏CARD 11和CARD 11相关信号成分的小鼠模型通常具有Treg缺陷,但一些小鼠模型发展明显的自身免疫和炎性疾病,而其他小鼠模型则没有。在肿瘤微环境中抑制TCR 4中的CARD 11信号传导可以潜在地促进抗肿瘤免疫。在这篇综述中,我们总结了CARD 11信号转导参与Treg发育和功能的证据,并讨论了关键的未回答的问题和未来的研究机会。
Regulatory T cells (Tregs) are a critical subset of CD4 T cells that modulate the immune response to prevent autoimmunity and chronic inflammation. CARD11, a signaling hub and scaffold protein that links antigen receptor engagement to activation of NF-κB and other downstream signaling pathways, is essential for the development and function of thymic Tregs. Mouse models with deficiencies in CARD11 and CARD11-associated signaling components generally have Treg defects, but some mouse models develop overt autoimmunity and inflammatory disease whereas others do not. Inhibition of CARD11 signaling in Tregs within the tumor microenvironment can potentially promote anti-tumor immunity. In this review, we summarize evidence for the involvement of CARD11 signaling in Treg development and function and discuss key unanswered questions and future research opportunities.
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