CAR-T cell therapy for lung cancer: Potential and perspective.
CAR-T cell therapy for lung cancer: Potential and perspective.
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DOI:
10.1111/1759-7714.14375
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发表时间:
2022-04
期刊:
影响因子:
2.9
通讯作者:
Huang Y
中科院分区:
文献类型:
--
作者:
Chen L;Chen F;Li J;Pu Y;Yang C;Wang Y;Lei Y;Huang Y
Lung cancer is the highest incidence and mortality of all cancers around the world. In the present immunotherapy era, an increasing number of immunotherapeutic agents including monoclonal antibody‐targeted drugs have been used in the clinical treatment of malignancy, but it still has many limitations. Chimeric antigen receptor‐modified T (CAR‐T) cells, a novel adoptive immunotherapy strategy, have not only been used successfully against hematological tumors, but have also opened up new avenues for immunotherapy of solid tumors, including lung cancer. However, targeting lung cancer‐specific antigens using engineered CAR‐T cells is complicated by the lack of proper tumor‐specific antigens, an immunosuppressive tumor microenvironment, a low level of CAR‐T cell infiltration into tumor tissues, along with off‐target effect, etc. Simultaneously, the clinical application of CAR‐T cells remains limited because of many challenges such as tumor lysis syndrome, neurotoxicity syndrome, and cytokine release syndrome. In this review, we outline the basic structure and generation characteristic of CAR‐T cells and summarize the common tumor‐associated antigens in clinical trials of CAR‐T cell therapy for lung cancer, and point out the current challenges and new strategies, aiming to provide new ideas and approaches for the pre‐clinical experiments and clinical trials of CAR‐T cell therapy in lung cancer. The clinical application process of CAR‐T cell immunotherapy. The clinical process of CAR T is as listed: T lymphocyte collection; CAR T‐cell manufacturing; CAR T‐cell amplification and screening in vitro; CAR‐T cells are infused back into patients; CAR‐T cells are transported to the tumor site and perform their function in the tumor microenvironment.
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影响因子:
1.3
作者:
Dong, Yanjun;Zheng, Xianjie;Zhang, Shuanglin
通讯作者:
Zhang, Shuanglin
DOI:
10.1016/s0140-6736(17)33326-3
发表时间:
2018-03-17
期刊:
Lancet (London, England)
影响因子:
--
作者:
Allemani C;Matsuda T;Di Carlo V;Harewood R;Matz M;Nikšić M;Bonaventure A;Valkov M;Johnson CJ;Estève J;Ogunbiyi OJ;Azevedo E Silva G;Chen WQ;Eser S;Engholm G;Stiller CA;Monnereau A;Woods RR;Visser O;Lim GH;Aitken J;Weir HK;Coleman MP;CONCORD Working Group
通讯作者:
CONCORD Working Group
DOI:
10.1038/mto.2016.11
发表时间:
2016
期刊:
Molecular therapy oncolytics
影响因子:
--
作者:
通讯作者:
--
DOI:
10.1056/nejmoa1200694
发表时间:
2012-06-28
期刊:
The New England journal of medicine
影响因子:
--
作者:
Brahmer JR;Tykodi SS;Chow LQ;Hwu WJ;Topalian SL;Hwu P;Drake CG;Camacho LH;Kauh J;Odunsi K;Pitot HC;Hamid O;Bhatia S;Martins R;Eaton K;Chen S;Salay TM;Alaparthy S;Grosso JF;Korman AJ;Parker SM;Agrawal S;Goldberg SM;Pardoll DM;Gupta A;Wigginton JM
通讯作者:
Wigginton JM
影响因子:
11.5
作者:
Gulati, Pratiksha;Ruhl, Julia;Petrausch, Ulf
通讯作者:
Petrausch, Ulf