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Neutralization of murine myeloid-derived suppressor cells enhances the efficacy of a chimeric antigen receptor T-cells directed against pediatric solid tumors

机译：鼠髓样来源的抑制细胞的中和作用增强了针对小儿实体瘤的嵌合抗原受体T细胞的功效

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1. Neutralization of murine myeloid-derived suppressor cells enhances the efficacy of a chimeric antigen receptor T-cells directed against pediatric solid tumors [J] . Steven L Highfill, Adrienne H Long, Rimas J Orentas, Journal for ImmunoTherapy of Cancer . 2013,第S1期

机译：鼠髓样来源的抑制细胞的中和作用增强了针对小儿实体瘤的嵌合抗原受体T细胞的功效
2. Enhancing Chimeric Antigen Receptor T-Cell Efficacy in Solid Tumors [J] . Fuca Giovanni, Reppel Loic, Landoni Elisa, Clinical cancer research: an official journal of the American Association for Cancer Research . 2020,第11期

机译：增强固体瘤中的嵌合抗原受体T细胞疗效
3. Multifactorial T-cell hypofunction that is reversible can limit the efficacy of chimeric antigen receptor-transduced human T cells in solid tumors [J] . MoonE.K., WangL.-C., DolfiD.V., Clinical cancer research: an official journal of the American Association for Cancer Research . 2014,第16期

机译：可逆的多因素T细胞功能低下可能会限制嵌合抗原受体转导的人T细胞在实体瘤中的功效
4. Main Issues and Current Strategies in Enhancing the Efficacy of Chimeric Antigen Receptor T-Cell Therapy among Tumor Treatments [C] . Zhengting He International Conference on Frontiers of Biological Sciences and Engineering . 2020

机译：提高嵌合抗原受体T细胞治疗肿瘤治疗疗效的主要问题及目前策略
5. Optimizing Chimeric Antigen Receptor (CAR) T Cells for an Enhanced and Broadened Anti-Tumor Immune Response Via Il-36γ [D] . Li, Xinghuo. 2020

机译：优化嵌合抗原受体（汽车）T细胞通过IL-36γ进行增强和扩大的抗肿瘤免疫应答
6. Neutralization of murine myeloid-derived suppressor cells enhances the efficacy of a chimeric antigen receptor T-cells directed against pediatric solid tumors [O] . Steven L Highfill, Adrienne H Long, Rimas J Orentas, 2013

机译：鼠髓样来源的抑制细胞的中和作用增强了针对小儿实体瘤的嵌合抗原受体T细胞的功效
7. Enhancing Chimeric Antigen Receptor T-Cell Efficacy in Solid Tumors [O] . Giovanni Fucà, Loic Reppel, Elisa Landoni, 2020

机译：增强固体瘤中的嵌合抗原受体T细胞疗效

Neutralization of murine myeloid-derived suppressor cells enhances the efficacy of a chimeric antigen receptor T-cells directed against pediatric solid tumors

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