Oncolytic Viruses: Therapeutics With an Identity Crisis

被引:70
作者
Breitbach, Caroline J. [1 ]
Lichty, Brian D. [1 ,2 ,3 ]
Bell, John C. [1 ,4 ]
机构
[1] Turnstone Biol, 787 Bank St, Ottawa, ON K1S 3V5, Canada
[2] McMaster Univ, Dept Pathol & Mol Med, McMaster Immunol Res Ctr, 1280 Main St, Hamilton, ON L8S 4K1, Canada
[3] McMaster Univ, MG DeGroote Inst Infect Dis Res, Hamilton, ON, Canada
[4] Ottawa Hosp Res Inst, Ctr Innovat Canc Therapeut, 501 Smyth Rd, Ottawa, ON K1H 8L6, Canada
关键词
Oncolytic virus; Oncolytic immunotherapy; In situ vaccine; Immune checkpoint inhibitors; CANCER; TUMOR; IMMUNOTHERAPY; VASCULATURE; VIROTHERAPY; EXPRESSION; RESPONSES; POXVIRUS; THERAPY; BETA;
D O I
10.1016/j.ebiom.2016.06.046
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Oncolytic viruses (OV) are replicating viral therapeutics for the treatment of cancer and have been in laboratory development for about twenty years. Recently, the FDA approved Imlygic, a herpes virus based therapeutic for the treatment of melanoma and thus OVs have entered a new era where they are a weapon in the armament of the oncologist. OVs are unique therapeutics with multiple mechanisms of therapeutic activity. The exact path for their development and eventual uptake by pharmaceutical companies is somewhat clouded by an uncertain identity. Are they vaccines, tumour lysing therapeutics, inducers of innate immunity, gene therapy vectors, anti-vascular agents or all of the above? Should they be developed as stand-alone loco-regional therapeutics, systemically delivered tumour hunters or immune modulators best tested as combination therapeutics? We summarize data here supporting the idea, depending upon the virus, that OVs can be any or all of these things. Pursuing a "one-size fits all" approach is counter-productive to their clinical development and instead as a field we should build on the strengths of individual virus platforms. (C) 2016 The Authors. Published by Elsevier B.V.
引用
收藏
页码:31 / 36
页数:6
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