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.
Original language | English |
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Pages (from-to) | 810-817 |
Number of pages | 8 |
Journal | International Journal of Clinical Oncology |
Volume | 25 |
Issue number | 5 |
DOIs | |
Publication status | Published - 2020 May 1 |
Keywords
- Immune checkpoint inhibitor
- Immunometabolism
- Microbiota
- Neo-antigen
- Oncogene
- TGF-β
ASJC Scopus subject areas
- Surgery
- Hematology
- Oncology