| Literature DB >> 27141345 |
Kristina Iribarren1, Norma Bloy2, Aitziber Buqué2, Isabelle Cremer1, Alexander Eggermont3, Wolf Hervé Fridman1, Jitka Fucikova4, Jérôme Galon5, Radek Špíšek4, Laurence Zitvogel6, Guido Kroemer7, Lorenzo Galluzzi8.
Abstract
Accumulating preclinical evidence indicates that Toll-like receptor (TLR) agonists efficiently boost tumor-targeting immune responses (re)initiated by most, if not all, paradigms of anticancer immunotherapy. Moreover, TLR agonists have been successfully employed to ameliorate the efficacy of various chemotherapeutics and targeted anticancer agents, at least in rodent tumor models. So far, only three TLR agonists have been approved by regulatory agencies for use in cancer patients. Moreover, over the past decade, the interest of scientists and clinicians in these immunostimulatory agents has been fluctuating. Here, we summarize recent advances in the preclinical and clinical development of TLR agonists for cancer therapy.Entities:
Keywords: Ampligen™; G100; Hiltonol™; bacillus Calmette-Guérin; imiquimod; motolimod
Year: 2015 PMID: 27141345 PMCID: PMC4839356 DOI: 10.1080/2162402X.2015.1088631
Source DB: PubMed Journal: Oncoimmunology ISSN: 2162-4011 Impact factor: 8.110