Combination therapy with CAR T cells and oncolytic viruses: a new era in cancer immunotherapy

被引:57
|
作者
Rezaei, Ramazan [1 ]
Esmaeili Gouvarchin Ghaleh, Hadi [1 ]
Farzanehpour, Mahdieh [1 ]
Dorostkar, Ruhollah [1 ]
Ranjbar, Reza [2 ]
Bolandian, Masoumeh [1 ]
Mirzaei Nodooshan, Majid [1 ]
Ghorbani Alvanegh, Akbar [3 ,4 ]
机构
[1] Baqiyatallah Univ Med Sci, Appl Virol Res Ctr, Tehran, Iran
[2] Baqiyatallah Univ Med Sci, Syst Biol & Poisonings Inst, Mol Biol Res Ctr, Tehran, Iran
[3] Human Genet Res Ctr, Tehran, Iran
[4] Baqiyatallah Univ Med Sci, Tehran, Iran
关键词
HERPES-SIMPLEX-VIRUS; ANTITUMOR IMMUNE-RESPONSES; MEASLES-VIRUS; SOLID TUMORS; PHASE-I; DENDRITIC CELLS; GENETIC-MODIFICATION; CROSS-PRESENTATION; VIRAL THERAPY; CD19; CAR;
D O I
10.1038/s41417-021-00359-9
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Chimeric antigen receptor (CAR) T-cell therapy is an encouraging and fast-growing platform used for the treatment of various types of tumors in human body. Despite the recent success of CAR T-cell therapy in hematologic malignancies, especially in B-cell lymphoma and acute lymphoblastic leukemia, the application of this treatment approach in solid tumors faced several obstacles resulted from the heterogeneous expression of antigens as well as the induction of immunosuppressive tumor microenvironment. Oncolytic virotherapy (OV) is a new cancer treatment modality by the use of competent or genetically engineered viruses to replicate in tumor cells selectively. OVs represent potential candidates to synergize the current setbacks of CAR T-cell application in solid tumors and then and overcome them. As well, the application of OVs gives researches the ability to engineer the virus with payloads in the way that it selectively deliver a specific therapeutic agents in tumor milieu to reinforce the cytotoxic activity of CAR T cells. Herein, we made a comprehensive review on the outcomes resulted from the combination of CAR T-cell immunotherapy and oncolytic virotherapy for the treatment of solid cancers. In the current study, we also provided brief details on some challenges that remained in this field and attempted to shed a little light on the future perspectives.
引用
收藏
页码:647 / 660
页数:14
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