| Literature DB >> 31919690 |
Yutaka Kawakami1,2, Shigeki Ohta3, Mohammad A Sayem3, Nobuo Tsukamoto3, Tomonori Yaguchi3.
Abstract
Immune checkpoint inhibitors (ICI) such as PD-1/PD-L1 antibodies (Abs) and CTLA4 Abs and T cell-based adoptive cell therapies are effective for patients with various cancers. However, response rates of ICI monotherapies are still limited due to lack of immunogenic antigens and various immune-resistant mechanisms. The latter includes adaptive immune resistance that is caused by anti-tumor T cells (e.g. PD-L1 induced by IFN-γ from T cells) and primary immune resistance that is caused by cancer cells (e.g. immunosuppressive cytokines produced by cancer cells). Further understanding of the immune-resistant mechanisms, which may be possible through comparative analyses of responders and non-responders to the immunotherapies, will lead to the identification of new diagnostic biomarkers and therapeutic targets for development of effective cancer immuno therapies.Entities:
Keywords: Immune checkpoint inhibitor; Immunometabolism; Microbiota; Neo-antigen; Oncogene; TGF-β
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Year: 2020 PMID: 31919690 DOI: 10.1007/s10147-019-01611-x
Source DB: PubMed Journal: Int J Clin Oncol ISSN: 1341-9625 Impact factor: 3.402