Adoptive immunotherapy with CAR modified T cells in cancer: current landscape and future perspectives

被引:14
作者
Coscia, Marta [1 ,2 ]
Vitale, Candida [1 ,2 ]
Cerrano, Marco [1 ,2 ]
Maffini, Enrico [3 ]
Giaccone, Luisa [2 ,4 ]
Bocca-Doro, Mario [1 ,2 ]
Bruno, Benedetto [2 ,4 ]
机构
[1] Univ Torino, Div Hematol, AOU Citta Salute & Sci Torino, Via Genova 3, I-10126 Turin, Italy
[2] Univ Torino, Dept Mol Biotechnol & Hlth Sci, Via Nizza 52, I-10126 Turin, Italy
[3] Romagna Transplant Network, Hematol & Stem Cell Transplant, Viale Randi 5, I-48121 Ravenna, Italy
[4] AOU Citta Salute & Sci Torino, SSD Trapianto Allogen Cellule Staminali, Dept Oncol, Via Genova 3, I-10126 Turin, Italy
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2019年 / 24卷
关键词
Chimeric antigen receptors T cells; CAR T cell therapy; Adoptive Immunotherapy; Review; CHIMERIC-ANTIGEN-RECEPTOR; ACUTE MYELOID-LEUKEMIA; B-CELL; ANTITUMOR-ACTIVITY; MULTIPLE-MYELOMA; HODGKIN-LYMPHOMA; TYROSINE KINASE; STEM-CELLS; NKT CELLS; THERAPY;
D O I
10.2741/4780
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cellular therapies are a rapidly evolving approach to treat cancer in the light of their unique mechanism of action that potentially overcomes drug resistance and induces durable remissions. Modalities of adoptive cell therapy include gene-modified T cells expressing novel T cell receptors or chimeric antigen receptors (CAR) that modify the immune system to recognize tumor cells and carry out potent antitumor effector functions. CAR T cells have shown very promising clinical results and several trials are being conducted worldwide to establish their role in cancer treatment. Most successful results have been observed in lymphoproliferative disorders with the use of CD19-directed CAR T cells, which led to their commercial approval by FDA. In this review, we provide a comprehensive overview of the current role of CAR T cell therapies in hematological malignancies and solid tumors, their associated toxicities and potential future developments in the armamentarium for cancer treatment.
引用
收藏
页码:1284 / 1315
页数:32
相关论文
共 202 条
[1]  
ABRAMSON JS, 2017, BLOOD S1, V130
[2]   IL-7 and CCL19 expression in CAR-T cells improves immune cell infiltration and CAR-T cell survival in the tumor [J].
Adachi, Keishi ;
Kano, Yosuke ;
Nagai, Tomohiko ;
Okuyama, Namiko ;
Sakoda, Yukimi ;
Tamada, Koji .
NATURE BIOTECHNOLOGY, 2018, 36 (04) :346-+
[3]   Allorecognition and the alloresponse: clinical implications [J].
Afzali, B. ;
Lechler, R. I. ;
Hernandez-Fuentes, M. P. .
TISSUE ANTIGENS, 2007, 69 (06) :545-556
[4]   HER2-Specific Chimeric Antigen Receptor-Modified Virus-Specific T Cells for Progressive Glioblastoma A Phase 1 Dose-Escalation Trial [J].
Ahmed, Nabil ;
Brawley, Vita ;
Hegde, Meenakshi ;
Bielamowicz, Kevin ;
Kalra, Mamta ;
Landi, Daniel ;
Robertson, Catherine ;
Gray, Tara L. ;
Diouf, Oumar ;
Wakefield, Amanda ;
Ghazi, Alexia ;
Gerken, Claudia ;
Yi, Zhongzhen ;
Ashoori, Aidin ;
Wu, Meng-Fen ;
Liu, Hao ;
Rooney, Cliona ;
Dotti, Gianpietro ;
Gee, Adrian ;
Su, Jack ;
Kew, Yvonne ;
Baskin, David ;
Zhang, Yi Jonathan ;
New, Pamela ;
Grilley, Bambi ;
Stojakovic, Milica ;
Hicks, John ;
Powell, Suzanne Z. ;
Brenner, Malcolm K. ;
Heslop, Helen E. ;
Grossman, Robert ;
Wels, Winfried S. ;
Gottschalk, Stephen .
JAMA ONCOLOGY, 2017, 3 (08) :1094-1101
[5]   Human Epidermal Growth Factor Receptor 2 (HER2) -Specific Chimeric Antigen Receptor-Modified T Cells for the Immunotherapy of HER2-Positive Sarcoma [J].
Ahmed, Nabil ;
Brawley, Vita S. ;
Hegde, Meenakshi ;
Robertson, Catherine ;
Ghazi, Alexia ;
Gerken, Claudia ;
Liu, Enli ;
Dakhova, Olga ;
Ashoori, Aidin ;
Corder, Amanda ;
Gray, Tara ;
Wu, Meng-Fen ;
Liu, Hao ;
Hicks, John ;
Rainusso, Nino ;
Dotti, Gianpietro ;
Mei, Zhuyong ;
Grilley, Bambi ;
Gee, Adrian ;
Rooney, Cliona M. ;
Brenner, Malcolm K. ;
Heslop, Helen E. ;
Wels, Winfried S. ;
Wang, Lisa L. ;
Anderson, Peter ;
Gottschalk, Stephen .
JOURNAL OF CLINICAL ONCOLOGY, 2015, 33 (15) :1688-+
[6]   Antitumor activity of CAR-T cells targeting the intracellular oncoprotein WT1 can be enhanced by vaccination [J].
Akahori, Yasushi ;
Wang, Linan ;
Yoneyama, Motohiro ;
Seo, Naohiro ;
Okumura, Satoshi ;
Miyahara, Yoshihiro ;
Amaishi, Yasunori ;
Okamoto, Sachiko ;
Mineno, Junichi ;
Ikeda, Hiroaki ;
Maki, Takehiro ;
Fujiwara, Hiroshi ;
Akatsuka, Yoshiki ;
Kato, Takuma ;
Shiku, Hiroshi .
BLOOD, 2018, 132 (11) :1134-1145
[7]  
[Anonymous], 2016, BLOOD
[8]  
[Anonymous], 2017, J CLIN ONCOL S
[9]  
[Anonymous], 2015, BLOOD
[10]  
[Anonymous], 2017, ASCO ABSTR