Engineering and combining oncolytic measles virus for cancer therapy

被引:36
|
作者
Leber, Mathias F. [1 ,2 ,3 ]
Neault, Serge [3 ]
Jirovec, Elise [3 ]
Barkley, Russell [3 ]
Said, Aida [4 ,5 ]
Bell, John C. [3 ]
Ungerechts, Guy [1 ,2 ,3 ]
机构
[1] German Canc Res Ctr, Clin Cooperat Unit Virotherapy, Neuenheimer Feld 280, D-69120 Heidelberg, Germany
[2] Heidelberg Univ Hosp, Dept Med Oncol, Neuenheimer Feld 460, D-69120 Heidelberg, Germany
[3] Ottawa Hosp Res Inst, Canc Therapeut Program, 501 Smyth Rd, Ottawa, ON K1H 8L6, Canada
[4] Childrens Hosp Eastern Ontario, 401 Smyth Rd, Ottawa, ON K1H 8L1, Canada
[5] Univ Ottawa, Fac Med, Dept Cellular & Mol Med, 451 Smyth Rd, Ottawa, ON K1H 8M5, Canada
关键词
Measles virus; Genetic engineering; Virotherapy; Oncolytic virus; Immunotherapy; Combination therapy; SODIUM-IODIDE SYMPORTER; CELLULAR IMMUNE-RESPONSES; VACCINE-STRAIN MEASLES; ANTITUMOR-ACTIVITY; TUMOR-CELLS; CARCINOEMBRYONIC ANTIGEN; ANTIBODY NEUTRALIZATION; GLYCOPROTEIN PROTECTS; SARS CORONAVIRUS; SECRETED FORM;
D O I
10.1016/j.cytogfr.2020.07.005
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
Cancer immunotherapy using tumor-selective, oncolytic viruses is an emerging therapeutic option for solid and hematologic malignancies. A considerable variety of viruses ranging from small picornaviruses to large pox viruses are currently being investigated as potential candidates. In the early days of virotherapy, non-engineered wild-type or vaccine-strain viruses were employed. However, these viruses often did not fully satisfy the major criteria of safety and efficacy. Since the advent of reverse genetics systems for manipulating various classes of viruses, the field has shifted to developing genetically engineered viruses with an improved therapeutic index. In this review, we will summarize the concepts and strategies of multi-level genetic engineering of oncolytic measles virus, a prime candidate for cancer immunovirotherapy. Furthermore, we will provide a brief overview of measles virus-based multimodal combination therapies for improved tumor control and clinical efficacy.
引用
收藏
页码:39 / 48
页数:10
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