| Literature DB >> 27757313 |
Erika Vacchelli1, Norma Bloy1, Fernando Aranda2, Aitziber Buqué1, Isabelle Cremer3, Sandra Demaria4, Alexander Eggermont5, Silvia Chiara Formenti4, Wolf Hervé Fridman3, Jitka Fucikova6, Jérôme Galon7, Radek Spisek6, Eric Tartour8, Laurence Zitvogel9, Guido Kroemer10, Lorenzo Galluzzi11.
Abstract
Malignant cells succumbing to some forms of radiation therapy are particularly immunogenic and hence can initiate a therapeutically relevant adaptive immune response. This reflects the intrinsic antigenicity of malignant cells (which often synthesize a high number of potentially reactive neo-antigens) coupled with the ability of radiation therapy to boost the adjuvanticity of cell death as it stimulates the release of endogenous adjuvants from dying cells. Thus, radiation therapy has been intensively investigated for its capacity to improve the therapeutic profile of several anticancer immunotherapies, including (but not limited to) checkpoint blockers, anticancer vaccines, oncolytic viruses, Toll-like receptor (TLR) agonists, cytokines, and several small molecules with immunostimulatory effects. Here, we summarize recent preclinical and clinical advances in this field of investigation.Keywords: Danger-associated molecular patterns; TGFβ1; immunogenic cell death; ipilimumab; nivolumab; pembrolizumab
Year: 2016 PMID: 27757313 PMCID: PMC5048768 DOI: 10.1080/2162402X.2016.1214790
Source DB: PubMed Journal: Oncoimmunology ISSN: 2162-4011 Impact factor: 8.110