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Acquired Resistance for Immune Checkpoint Inhibitors in Cancer Immunotherapy: Challenges and Prospects

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Specialty Geriatrics
Date 2022 Jan 17
PMID 35037899
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Abstract

Drug resistance has become an obstacle to the further development of immunotherapy in clinical applications and experimental studies. In the current review, the acquired resistance to immunotherapy was examined. The mechanisms of acquired resistance were based on three aspects as follows: The change of the tumor functions, the upregulated expression of inhibitory immune checkpoint proteins, and the effects of the tumor microenvironment. The combined use of immunotherapy and other therapies is performed to delay acquired resistance. A comprehensive understanding of acquired drug resistance may provide ideas for solving this dilemma.

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References
1.
Brennan C, Garrett W . Fusobacterium nucleatum - symbiont, opportunist and oncobacterium. Nat Rev Microbiol. 2018; 17(3):156-166. PMC: 6589823. DOI: 10.1038/s41579-018-0129-6. View

2.
Zou R, Wang Y, Ye F, Zhang X, Wang M, Cui S . Mechanisms of primary and acquired resistance to PD-1/PD-L1 blockade and the emerging role of gut microbiome. Clin Transl Oncol. 2021; 23(11):2237-2252. DOI: 10.1007/s12094-021-02637-2. View

3.
Andrews L, Yano H, Vignali D . Inhibitory receptors and ligands beyond PD-1, PD-L1 and CTLA-4: breakthroughs or backups. Nat Immunol. 2019; 20(11):1425-1434. DOI: 10.1038/s41590-019-0512-0. View

4.
Salmon H, Franciszkiewicz K, Damotte D, Dieu-Nosjean M, Validire P, Trautmann A . Matrix architecture defines the preferential localization and migration of T cells into the stroma of human lung tumors. J Clin Invest. 2012; 122(3):899-910. PMC: 3287213. DOI: 10.1172/JCI45817. View

5.
Anagnostou V, Smith K, Forde P, Niknafs N, Bhattacharya R, White J . Evolution of Neoantigen Landscape during Immune Checkpoint Blockade in Non-Small Cell Lung Cancer. Cancer Discov. 2016; 7(3):264-276. PMC: 5733805. DOI: 10.1158/2159-8290.CD-16-0828. View