骨髓生成
髓样
癌症研究
封锁
癌症
医学
髓系细胞
癌细胞
程序性细胞死亡
免疫系统
免疫检查点
免疫学
免疫疗法
细胞凋亡
生物
内科学
造血
细胞生物学
受体
干细胞
生物化学
作者
Mai Fujiwara,Lucien P. Garo,Gopal Murugaiyan
标识
DOI:10.1016/j.trecan.2020.02.018
摘要
Programmed death 1 (PD1) has emerged as a major inhibitor of antitumor T cells, and anti-PD1 therapies have demonstrated clinical efficacy in multiple cancers. However, the impact of PD1 on other immune cells had remained unclear. A recent study by Strauss et al. describes how myeloid cell-intrinsic PD1 signaling limits myelopoiesis in cancer pertinent to anti-PD1 therapies. Programmed death 1 (PD1) has emerged as a major inhibitor of antitumor T cells, and anti-PD1 therapies have demonstrated clinical efficacy in multiple cancers. However, the impact of PD1 on other immune cells had remained unclear. A recent study by Strauss et al. describes how myeloid cell-intrinsic PD1 signaling limits myelopoiesis in cancer pertinent to anti-PD1 therapies.
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