| Literature DB >> 27057469 |
Jonathan Pol1, Aitziber Buqué1, Fernando Aranda2, Norma Bloy1, Isabelle Cremer3, Alexander Eggermont4, Philippe Erbs5, Jitka Fucikova6, Jérôme Galon7, Jean-Marc Limacher5, Xavier Preville5, Catherine Sautès-Fridman3, Radek Spisek6, Laurence Zitvogel8, Guido Kroemer9, Lorenzo Galluzzi1.
Abstract
Oncolytic virotherapy relies on the administration of non-pathogenic viral strains that selectively infect and kill malignant cells while favoring the elicitation of a therapeutically relevant tumor-targeting immune response. During the past few years, great efforts have been dedicated to the development of oncolytic viruses with improved specificity and potency. Such an intense wave of investigation has culminated this year in the regulatory approval by the US Food and Drug Administration (FDA) of a genetically engineered oncolytic viral strain for use in melanoma patients. Here, we summarize recent preclinical and clinical advances in oncolytic virotherapy.Entities:
Keywords: Cavatak™; GM-CSF; JX-594; ONCOS-102; Reolysin®; talimogene laherparepvec
Year: 2015 PMID: 27057469 PMCID: PMC4801444 DOI: 10.1080/2162402X.2015.1117740
Source DB: PubMed Journal: Oncoimmunology ISSN: 2162-4011 Impact factor: 8.110