| Literature DB >> 29275092 |
Shashi Gujar1, Jonathan G Pol2, Youra Kim3, Patrick W Lee4, Guido Kroemer5.
Abstract
Oncolytic viruses (OVs) represent a new class of cancer immunotherapeutics. Administration of OVs to cancer-bearing hosts induces two distinct immunities: antiviral and antitumor. While antitumor immunity is beneficial, antiviral immune responses are often considered detrimental for the efficacy of OV-based therapy. The existing dogma postulates that anti-OV immune responses restrict viral replication and spread, and thus reduce direct OV-mediated killing of cancer cells. Accordingly, a myriad of therapeutic strategies aimed at mitigating anti-OV immune responses is presently being tested. Here, we advocate that OV-induced antiviral immune responses hold intrinsic anticancer benefits and are essential for establishing clinically desired antitumor immunity. Thus, to achieve the optimal efficacy of OV-based cancer immunotherapies, strategic management of anti-OV immune responses is of critical importance.Entities:
Mesh:
Substances:
Year: 2017 PMID: 29275092 DOI: 10.1016/j.it.2017.11.006
Source DB: PubMed Journal: Trends Immunol ISSN: 1471-4906 Impact factor: 16.687