Iribarren Kristina, Bloy Norma, Buqué Aitziber, Cremer Isabelle, Eggermont Alexander, Fridman Wolf Hervé, Fucikova Jitka, Galon Jérôme, Špíšek Radek, Zitvogel Laurence, Kroemer Guido, Galluzzi Lorenzo
INSERM, U1138, Paris, France; Equipe 13, Center de Recherche des Cordeliers, Paris, France; Université Pierre et Marie Curie/Paris VI, Paris, France.
INSERM, U1138, Paris, France; Gustave Roussy Cancer Campus, Villejuif, France; Equipe 11 labellisée par la Ligue Nationale contre le Cancer, Center de Recherche des Cordeliers, Paris, France.
Oncoimmunology. 2015 Sep 2;5(3):e1088631. doi: 10.1080/2162402X.2015.1088631. eCollection 2016 Mar.
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.
越来越多的临床前证据表明,Toll样受体(TLR)激动剂能有效增强由大多数(即便不是全部)抗癌免疫治疗范式引发的肿瘤靶向免疫反应。此外,至少在啮齿动物肿瘤模型中,TLR激动剂已成功用于改善各种化疗药物和靶向抗癌药物的疗效。到目前为止,只有三种TLR激动剂已获监管机构批准用于癌症患者。此外,在过去十年中,科学家和临床医生对这些免疫刺激剂的兴趣一直在波动。在此,我们总结了TLR激动剂用于癌症治疗的临床前和临床开发的最新进展。