| Literature DB >> 31974169 |
Annabelle J Anandappa1,2,3, Catherine J Wu1,2,4,5, Patrick A Ott6,2,4,5.
Abstract
Although immune checkpoint inhibitors (ICI) have demonstrated clinical activity in multiple tumor types, the majority of patients do not respond to ICI monotherapy. Mounting evidence suggests that ICI-mediated clinical responses rely upon tumor infiltration by T cells that are able to recognize and kill cancer cells. Here, we review therapeutic modalities that have been shown to promote T-cell infiltration into human tumors in studies to date, and discuss emerging data guiding how these modalities can be sequenced in order to optimize T-cell effector function and memory T-cell generation, while minimizing overactivation and potential toxicity. SIGNIFICANCE: The lack of preexisting T-cell inflammation in tumors is a major barrier to effective cancer immunity. A deep understanding of the mechanisms that prevent T cells from trafficking into the tumor in a given individual will be critical for tailoring immunotherapy combinations that can overcome resistance to ICI in patients with cancer. ©2020 American Association for Cancer Research.Entities:
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Year: 2020 PMID: 31974169 PMCID: PMC7007384 DOI: 10.1158/2159-8290.CD-19-0790
Source DB: PubMed Journal: Cancer Discov ISSN: 2159-8274 Impact factor: 38.272