Tuning CARs: recent advances in modulating chimeric antigen receptor (CAR) T cell activity for improved safety, efficacy, and flexibility

被引:0
作者
Piotr Celichowski
Marcello Turi
Sandra Charvátová
Dhwani Radhakrishnan
Neda Feizi
Zuzana Chyra
Michal Šimíček
Tomáš Jelínek
Juli Rodriguez Bago
Roman Hájek
Matouš Hrdinka
机构
[1] University of Ostrava,Department of Haematooncology, Faculty of Medicine
[2] University Hospital Ostrava,Department of Haematooncology
[3] University of Ostrava,Faculty of Science
[4] Sapienza University of Rome,Department of Internal Clinical Sciences, Anesthesiology and Cardiovascular Sciences
来源
Journal of Translational Medicine | / 21卷
关键词
Chimeric antigen receptor; CAR; Cancer; Immunotherapy; T cell; Synthetic; Regulation; Cell therapy;
D O I
暂无
中图分类号
学科分类号
摘要
Cancer immunotherapies utilizing genetically engineered T cells have emerged as powerful personalized therapeutic agents showing dramatic preclinical and clinical results, particularly in hematological malignancies. Ectopically expressed chimeric antigen receptors (CARs) reprogram immune cells to target and eliminate cancer. However, CAR T cell therapy's success depends on the balance between effective anti-tumor activity and minimizing harmful side effects. To improve CAR T cell therapy outcomes and mitigate associated toxicities, scientists from different fields are cooperating in developing next-generation products using the latest molecular cell biology and synthetic biology tools and technologies. The immunotherapy field is rapidly evolving, with new approaches and strategies being reported at a fast pace. This comprehensive literature review aims to provide an up-to-date overview of the latest developments in controlling CAR T cell activity for improved safety, efficacy, and flexibility.
引用
收藏
相关论文
共 1077 条
[1]  
Cartellieri M(2016)Switching CAR T cells on and off: a novel modular platform for retargeting of T cells to AML blasts Blood Cancer J 6 e458-67
[2]  
Feldmann A(2015)Identification of chimeric antigen receptors that mediate constitutive or inducible proliferation of T cells Cancer Immunol Res 3 356-9
[3]  
Koristka S(2010)Adverse events following infusion of T cells for adoptive immunotherapy: a 10-year experience Cytotherapy 12 743-51
[4]  
Arndt C(2010)Case report of a serious adverse event following the administration of T cells transduced with a chimeric antigen receptor recognizing ERBB2 Mol Ther 18 843-8
[5]  
Loff S(2014)CD19-CAR trials Cancer J 20 112-83
[6]  
Ehninger A(2016)Therapeutic potential of T cell chimeric antigen receptors (CARs) in cancer treatment: counteracting off-tumor toxicities for safe CAR T cell therapy Annu Rev Pharmacol Toxicol 56 59-47
[7]  
Frigault MJ(2017)Avoidance of on-target off-tumor activation using a co-stimulation-only chimeric antigen receptor Mol Ther 25 1234-306
[8]  
Lee J(2017)Kinetics and biomarkers of severe cytokine release syndrome after CD19 chimeric antigen receptor-modified T-cell therapy Blood 130 2295-62
[9]  
Basil MC(2018)Chimeric antigen receptor T-cell therapy—assessment and management of toxicities Nat Rev Clin Oncol 15 47-37
[10]  
Carpenito C(2019)Teaching an old dog new tricks: next-generation CAR T cells Br J Cancer 120 26-27