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Selective HDAC6 inhibitors improve anti-PD-1 immune checkpoint blockade therapy by decreasing the anti-inflammatory phenotype of macrophages and down-regulation of immunosuppressive proteins in tumor cells
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SYSNO ASEP 0510823 Druh ASEP J - Článek v odborném periodiku Zařazení RIV J - Článek v odborném periodiku Poddruh J Článek ve WOS Název Selective HDAC6 inhibitors improve anti-PD-1 immune checkpoint blockade therapy by decreasing the anti-inflammatory phenotype of macrophages and down-regulation of immunosuppressive proteins in tumor cells Tvůrce(i) Knox, T. (US)
Sahakian, E. (US)
Banik, D. (US)
Hadley, M. (US)
Palmer, E. (US)
Noonepalle, S. (US)
Kim, J. (US)
Powers, J. (US)
Gracia-Hernandez, M. (US)
Oliveira, V. (US)
Cheng, F. (US)
Chen, J. (US)
Bařinka, Cyril (BTO-N) RID, ORCID
Pinilla-Ibarz, J. (US)
Lee, N. H. (US)
Kozikowski, A. (US)
Villagra, A. (US)Celkový počet autorů 17 Číslo článku 6136 Zdroj.dok. Scientific Reports. - : Nature Publishing Group - ISSN 2045-2322
Roč. 9, APR 16 2019 (2019)Poč.str. 17 s. Jazyk dok. eng - angličtina Země vyd. GB - Velká Británie Klíč. slova HISTONE DEACETYLASE 6 ; LIGAND 1 EXPRESSION ; INFILTRATING LYMPHOCYTES Vědní obor RIV EB - Genetika a molekulární biologie Obor OECD Biochemistry and molecular biology Způsob publikování Open access Institucionální podpora BTO-N - RVO:86652036 UT WOS 000464652400007 EID SCOPUS 85064568265 DOI 10.1038/s41598-019-42237-3 Anotace Histone deacetylases (HDACs) are involved in diverse cellular regulatory mechanisms including non-canonical functions outside the chromatin environment. Several publications have demonstrated that selective HDAC inhibitors (HDACi) can influence tumor immunogenicity and the functional activity of specific immune cells. In particular, the selective inhibition of HDAC6 has been reported to decrease tumor growth in several malignancies. However, there is still no clarity about the cellular components mediating this effect. In this study, we evaluated the HDAC6i Nexturastat A as a priming agent to facilitate the transition of the tumor microenvironment from cold to hot, and potentially augment immune check-point blockade therapies. This combination modality demonstrated to significantly reduce tumor growth in syngeneic melanoma tumor models. Additionally, we observed a complete neutralization of the up-regulation of PD-L1 and other immunosuppressive pathways induced by the treatment with anti-PD-1 blockade. This combination also showed profound changes in the tumor microenvironment such as enhanced infiltration of immune cells, increased central and effector T cell memory, and a significant reduction of pro-tumorigenic M2 macrophages. The evaluation of individual components of the tumor microenvironment suggested that the in vivo anti-tumor activity of HDAC6i is mediated by its effect on tumor cells and tumor-associated macrophages, and not directly over T cells. Overall, our results indicate that selective HDAC6i could be used as immunological priming agents to sensitize immunologically cold tumors and subsequently improve ongoing immune check-point blockade therapies. Pracoviště Biotechnologický ústav Kontakt Monika Kopřivová, Monika.Koprivova@ibt.cas.cz, Tel.: 325 873 700 Rok sběru 2020 Elektronická adresa https://www.nature.com/articles/s41598-019-42237-3
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