Harnessing natural killer cell effector function against cancer.

Harnessing natural killer cell effector function against cancer.
复制标题

DOI:
10.1093/immadv/ltad031
复制
发表时间:
2024
影响因子:
--
通讯作者:
--
中科院分区:
其他
文献类型:
--
作者:

文献摘要

参考文献

相似文献

自然杀伤(NK)细胞是参与抗肿瘤和抗病毒免疫应答的细胞毒性先天淋巴细胞。它们快速破坏异常细胞并增强树突状细胞、CD8+ T细胞和巨噬细胞的抗癌功能的能力使它们成为免疫策略的有吸引力的靶标。增强NK细胞活化对抗癌症的方法的开发目前正在进行紧张的临床前和临床研究,并且策略包括嵌合抗原受体NK细胞、NK细胞增殖剂、细胞因子和免疫检查点抑制剂。在这篇综述中,我们强调了NK细胞治疗发展的最新进展,并讨论了它们对我们抗癌的潜力。
Natural killer (NK) cells are cytotoxic innate lymphoid cells that participate in anti-tumour and anti-viral immune responses. Their ability to rapidly destroy abnormal cells and to enhance the anti-cancer function of dendritic cells, CD8+ T cells, and macrophages makes them an attractive target for immunotherapeutic strategies. The development of approaches that augment NK-cell activation against cancer is currently under intense preclinical and clinical research and strategies include chimeric antigen receptor NK cells, NK-cell engagers, cytokines, and immune checkpoint inhibitors. In this review, we highlight recent advances in NK-cell therapeutic development and discuss their potential to add to our armamentarium against cancer.
DOI: 10.1073/pnas.2301606120
发表时间: 2023-06-27
影响因子: 11.1
作者:
Ben-Akiva, Elana;Karlsson, Johan;Hemmati, Shayan;Yu, Hongzhe;Tzeng, Stephany Y.;Pardoll, Drew M.;Green, Jordan J.
通讯作者: Green, Jordan J.
DOI: 10.1016/j.cell.2019.02.005
发表时间: 2019-04-18
期刊: CELL
影响因子: 64.5
作者:
Binnewies, Mikhail;Mujal, Adriana M.;Krummel, Matthew F.
通讯作者: Krummel, Matthew F.
DOI: 10.4049/jimmunol.179.8.5033
发表时间: 2007-10-15
影响因子: 4.4
作者:
Bijker, Martijn S.;van den Eeden, Susan J. F.;van der Burg, Sjoerd H.
通讯作者: van der Burg, Sjoerd H.
DOI: 10.1126/scitranslmed.abn3464
发表时间: 2023-03-08
影响因子: 17.1
作者:
da Silva, Jamile Ramos;Rodrigues, Karine Bitencourt;Ferreira, Luis Carlos de Souza
通讯作者: Ferreira, Luis Carlos de Souza
癌症免疫疗法。树突状细胞疫苗增加了黑色素瘤新抗原特异性T细胞的广度和多样性。
DOI: 10.1126/science.aaa3828
发表时间: 2015-05-15
期刊: Science (New York, N.Y.)
影响因子: --
作者:
Carreno BM;Magrini V;Becker-Hapak M;Kaabinejadian S;Hundal J;Petti AA;Ly A;Lie WR;Hildebrand WH;Mardis ER;Linette GP
通讯作者: Linette GP