scholarly journals Chimeric antigen receptor T cell targeting EGFRvIII for metastatic lung cancer therapy

2019 ◽  
Vol 13 (1) ◽  
pp. 57-68 ◽  
Author(s):  
Zhao Zhang ◽  
Jun Jiang ◽  
Xiaodong Wu ◽  
Mengyao Zhang ◽  
Dan Luo ◽  
...  
2015 ◽  
Vol 34 (2) ◽  
pp. 291-301 ◽  
Author(s):  
Dalit Landesman-Milo ◽  
Srinivas Ramishetti ◽  
Dan Peer

2019 ◽  
Vol 295 ◽  
pp. 153-163 ◽  
Author(s):  
Caina Xu ◽  
Yanbing Wang ◽  
Zhaopei Guo ◽  
Jie Chen ◽  
Lin Lin ◽  
...  

2022 ◽  
Vol 16 ◽  
pp. 101309
Author(s):  
Xiao-Hong Chen ◽  
Ruo Chen ◽  
Ming-Yan Shi ◽  
Ruo-Fei Tian ◽  
Hai Zhang ◽  
...  

2021 ◽  
Vol 12 ◽  
Author(s):  
Bu-Fan Xiao ◽  
Jing-Tao Zhang ◽  
Yu-Ge Zhu ◽  
Xin-Run Cui ◽  
Zhe-Ming Lu ◽  
...  

Chimeric antigen receptor T (CAR-T) cell therapy has exhibited a substantial clinical response in hematological malignancies, including B-cell leukemia, lymphoma, and multiple myeloma. Therefore, the feasibility of using CAR-T cells to treat solid tumors is actively evaluated. Currently, multiple basic research projects and clinical trials are being conducted to treat lung cancer with CAR-T cell therapy. Although numerous advances in CAR-T cell therapy have been made in hematological tumors, the technology still entails considerable challenges in treating lung cancer, such as on−target, of−tumor toxicity, paucity of tumor-specific antigen targets, T cell exhaustion in the tumor microenvironment, and low infiltration level of immune cells into solid tumor niches, which are even more complicated than their application in hematological tumors. Thus, progress in the scientific understanding of tumor immunology and improvements in the manufacture of cell products are advancing the clinical translation of these important cellular immunotherapies. This review focused on the latest research progress of CAR-T cell therapy in lung cancer treatment and for the first time, demonstrated the underlying challenges and future engineering strategies for the clinical application of CAR-T cell therapy against lung cancer.


Cancers ◽  
2020 ◽  
Vol 12 (3) ◽  
pp. 706 ◽  
Author(s):  
Aline Pfefferle ◽  
Nicholas D. Huntington

The clinical success stories of chimeric antigen receptor (CAR)-T cell therapy against B-cell malignancies have contributed to immunotherapy being at the forefront of cancer therapy today. Their success has fueled interest in improving CAR constructs, identifying additional antigens to target, and clinically evaluating them across a wide range of malignancies. However, along with the exciting potential of CAR-T therapy comes the real possibility of serious side effects. While the FDA has approved commercialized CAR-T cell therapy, challenges associated with manufacturing, costs, and related toxicities have resulted in increased attention being paid to implementing CAR technology in innate cytotoxic natural killer (NK) cells. Here, we review the current landscape of the CAR-NK field, from successful clinical implementation to outstanding challenges which remain to be addressed to deliver the full potential of this therapy to more patients.


2017 ◽  
Author(s):  
Edwin J. Velazquez ◽  
Kiara Vaden ◽  
Michelle H. Townsend ◽  
Evita G. Weagel ◽  
Scott Weber ◽  
...  

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