| Literature DB >> 27332730 |
Jonathan M Pitt1, Marie Vétizou1, Romain Daillère1, María Paula Roberti2, Takahiro Yamazaki2, Bertrand Routy1, Patricia Lepage3, Ivo Gomperts Boneca4, Mathias Chamaillard5, Guido Kroemer6, Laurence Zitvogel7.
Abstract
Inhibition of immune regulatory checkpoints, such as CTLA-4 and the PD-1-PD-L1 axis, is at the forefront of immunotherapy for cancers of various histological types. However, such immunotherapies fail to control neoplasia in a significant proportion of patients. Here, we review how a range of cancer-cell-autonomous cues, tumor-microenvironmental factors, and host-related influences might account for the heterogeneous responses and failures often encountered during therapies using immune-checkpoint blockade. Furthermore, we describe the emerging evidence of how the strong interrelationship between the immune system and the host microbiota can determine responses to cancer therapies, and we introduce a concept by which prior or concomitant modulation of the gut microbiome could optimize therapeutic outcomes upon immune-checkpoint blockade.Entities:
Keywords: CTLA-4; PD-1; PD-L1; cancer; immune-checkpoint blockade; immunotherapy; immunotherapy resistance; ipilimumab; microbiome; microbiota
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Year: 2016 PMID: 27332730 DOI: 10.1016/j.immuni.2016.06.001
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745