生物
免疫系统
免疫识别
免疫学
计算生物学
细胞生物学
癌症研究
作者
Fuguo Liu,Rizwan Romee
标识
DOI:10.1016/j.stem.2024.07.005
摘要
CD54 and CD58 are adhesion proteins that mediate efficient immune synapse formation. Hammer et al. now show that the abrogation of these molecules in T and NK cells prevents their immune rejection while maintaining their effector function. These findings should significantly help advance our efforts to generate "off-the-shelf" allogeneic products.
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