CD8型
细胞毒性T细胞
细胞生物学
T细胞
生物
ZAP70型
免疫系统
抗原提呈细胞
功能(生物学)
癌症研究
自然杀伤性T细胞
白细胞介素21
免疫学
白细胞介素2受体
分子生物学
受体
抑制器
细胞
髓源性抑制细胞
TCIRG1公司
电池类型
肿瘤坏死因子α
髓样
免疫耐受
树突状细胞
白细胞介素3
化学
T淋巴细胞
配体(生物化学)
作者
Jeong-su Do,Wei‐Kai Chen,Yu‐Wen Hung,David Arribas-Layton,Congcong Lu,Angel Gu,Enrique Montero,Alexandre M. Carmo,Helena Reijonen
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2026-01-23
卷期号:12 (4): eadz4203-eadz4203
标识
DOI:10.1126/sciadv.adz4203
摘要
CUB domain–containing protein 1 (CDCP1; CD318) is a surface glycoprotein known as a ligand for CD6, primarily studied in tumor immunology where it associates with poor prognosis. CD318 is expressed in myeloid dendritic cells and activated monocytes associated with immunoregulatory functions. Here, selective expression of CD318 on a subset of activated human CD8 + T cells, but not CD4 + T cells, is shown, defining suppressor function of this cell population. CD318 + CD8 T cells exhibited reduced PD-1 and KLRG-1 expression, diminished interferon-γ and tumor necrosis factor–α production, and potent suppression of autologous CD4 and CD8 T cell activation in vitro. Notably, CD8 T cells from patients with type 1 diabetes (T1D) showed reduced CD318 induction compared with controls. Mechanistically, CD318 inhibited T cell receptor signaling independently of SHP2, while its induction required interleukin-2–dependent mTOR activation. These findings identify CD318 as a marker of human CD8 + T cells with implications for immune regulation and autoimmunity.
科研通智能强力驱动
Strongly Powered by AbleSci AI