细胞毒性T细胞
CD1D公司
CD8型
效应器
免疫系统
T细胞受体
T细胞
抗原提呈细胞
生物
免疫学
化学
细胞生物学
自然杀伤性T细胞
生物化学
体外
作者
David Dunkin,Francesco Merlino,Carmen Correale,Garabet Yeretssian,Luciana Marinelli,Giulia Roda
标识
DOI:10.1053/j.gastro.2022.06.025
摘要
Intestinal epithelial cells (IECs) play a pivotal role in controlling immune responses by activation of suppressive CD8+ T regulatory (Treg) cells.1,2 Indeed, we have shown that at homeostasis, IECs interact with CD8+ T cells through a complex formed by CEACAM5 and CD1d on IECs and CD8α and T-cell receptor (TCR) on CD8+ T cells.2 CEACAM5 interacts with CD8α through its N-domain, and it is the only CEACAM family member that interacts with CD1d through its B3-domain.1 This unique set of interactions facilitates antigen presentation by CD1d to T cells, allowing the subsequent activation of CD8+ Treg cells, which possess a potent function in suppressing effector T cell responses and hence are essential to prevent autoimmune disorders.
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