
Trends in Molecular Medicine, Journal Year: 2023, Volume and Issue: 29(11), P. 897 - 911
Published: Sept. 11, 2023
Language: Английский
Trends in Molecular Medicine, Journal Year: 2023, Volume and Issue: 29(11), P. 897 - 911
Published: Sept. 11, 2023
Language: Английский
Immunity, Journal Year: 2023, Volume and Issue: 56(7), P. 1613 - 1630.e5
Published: June 30, 2023
Language: Английский
Citations
105Cancer Cell, Journal Year: 2024, Volume and Issue: 42(8), P. 1415 - 1433.e12
Published: July 18, 2024
Language: Английский
Citations
23Nature reviews. Immunology, Journal Year: 2025, Volume and Issue: unknown
Published: Jan. 2, 2025
Language: Английский
Citations
8Seminars in Cancer Biology, Journal Year: 2025, Volume and Issue: 109, P. 44 - 66
Published: Jan. 9, 2025
Language: Английский
Citations
3BioDrugs, Journal Year: 2025, Volume and Issue: unknown
Published: Feb. 15, 2025
Immunotherapy with checkpoint inhibitors has become the cornerstone of systemic treatment for non-oncogene addicted non-small-cell lung cancer. Despite its pivotal role, a significant proportion patients—approximately 70–85%—either exhibit primary resistance to PD-1 blockade or develop acquired following an initial benefit, even in combination chemotherapy and/or anti-CTLA-4 agents. The phenomenon and immunotherapy represents critical clinical challenge, largely based on our incomplete understanding mechanisms action immunotherapy, resulting lack accurate predictive biomarkers. Here, we review definitions explore proposed resistance, including those related tumor microenvironment, factors, intrinsic characteristics. We also discuss translational data adaptive changes within cells immune infiltrate exposure inhibitors. Lastly, offer comprehensive overview current emerging therapeutic strategies designed prevent counteract resistance.
Language: Английский
Citations
2Nature reviews. Immunology, Journal Year: 2023, Volume and Issue: 24(5), P. 358 - 374
Published: Dec. 14, 2023
Language: Английский
Citations
29International Journal of Molecular Sciences, Journal Year: 2023, Volume and Issue: 24(7), P. 6710 - 6710
Published: April 4, 2023
Cancer is one of the leading causes death in world; therefore, extensive research has been dedicated to exploring potential therapeutics, including immune checkpoint inhibitors (ICIs). Initially, programmed-death ligand-1 was biomarker utilized predict efficacy ICIs. However, its heterogeneous expression tumor microenvironment, which critical cancer progression, promoted exploration mutation burden (TMB). Research various cancers, such as melanoma and lung cancer, shown an association between high TMB response ICIs, increasing predictive value. failed ICI numerous other cancers. Therefore, future needed analyze variations types establish cutoffs order create a more standardized methodology for using clinically. In this review, we aim explore current on biomarker, discuss approaches overcoming immunoresistance highlight new trends field liquid biopsies, next generation sequencing, chimeric antigen receptor T-cell therapy, personalized vaccines.
Language: Английский
Citations
28Nature Cancer, Journal Year: 2023, Volume and Issue: 4(7), P. 1016 - 1035
Published: July 10, 2023
Language: Английский
Citations
27Nature Communications, Journal Year: 2024, Volume and Issue: 15(1)
Published: March 13, 2024
Abstract Cross-presentation by type 1 DCs (cDC1) is critical to induce and sustain antitumoral CD8 T cell responses model antigens, in various tumor settings. However, the impact of cross-presenting cDC1 potential DC-based therapies tumors carrying varied levels bona-fide neoantigens (neoAgs) remain unclear. Here we develop a hypermutated non-small lung cancer female mice, encoding genuine MHC-I neoepitopes study neoAgs-specific spontaneous settings upon Flt3L + αCD40 (DC-therapy). We find that are required generate broad against range diverse neoAgs. DC-therapy promotes immunogenicity weaker neoAgs strongly inhibits growth high tumor-mutational burden (TMB) tumors. In contrast, low TMB respond poorly DC-therapy, generating mild not sufficient block progression. scRNA transcriptional analysis, immune profiling functional assays unveil changes induced tissues, which comprise accumulation with increased immunostimulatory properties less exhausted effector cells. conclude boosting activity broaden diversity anti-tumoral leverage content for therapeutic advantage.
Language: Английский
Citations
15Nature reviews. Cancer, Journal Year: 2024, Volume and Issue: 24(6), P. 363 - 381
Published: April 11, 2024
Language: Английский
Citations
14