Impact of HDAC inhibitors on macrophage polarization to enhance innate immunity against infections
Faizan, B. M., Srdanović, S., Sundberg, L.-R., Kristín, E. H., Marjomäki, V., & Dekker, F. J. (2024). Impact of HDAC inhibitors on macrophage polarization to enhance innate immunity against infections. Drug Discovery Today, 29(11), Article 104193. https://doi.org/10.1016/j.drudis.2024.104193
Julkaistu sarjassa
Drug Discovery TodayTekijät
Päivämäärä
2024Tekijänoikeudet
2024 The Author(s). Published by Elsevier Ltd.
Innate immunity plays an important role in host defense against pathogenic infections. It involves macrophage polarization into either the pro-inflammatory M1 or the anti-inflammatory M2 phenotype, influencing immune stimulation or suppression, respectively. Epigenetic changes during immune reactions contribute to long-term innate immunity imprinting on macrophage polarization. It is becoming increasingly evident that epigenetic modulators, such as histone deacetylase (HDAC) inhibitors (HDACi), enable the enhancement of innate immunity by tailoring macrophage polarization in response to immune stressors. In this review, we summarize current literature on the impact of HDACi and other epigenetic modulators on the functioning of macrophages during diseases that have a strong immune component, such as infections. Depending on the disease context and the chosen therapeutic intervention, HDAC1, HDAC2, HDAC3, HDAC6, or HDAC8 are particularly important in influencing macrophage polarization towards either M1 or M2 phenotypes. We anticipate that therapeutic strategies based on HDAC epigenetic mechanisms will provide a unique approach to boost immunity against disease challenges, including resistant infections.
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Julkaisija
ElsevierISSN Hae Julkaisufoorumista
1359-6446Asiasanat
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https://converis.jyu.fi/converis/portal/detail/Publication/243253548
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Euroopan komissioRahoitusohjelmat(t)
The content of the publication reflects only the author’s view. The funder is not responsible for any use that may be made of the information it contains.
Lisätietoja rahoituksesta
We acknowledge funding granted to the authors by the European Union for the IN-ARMOR project (Project No. 101080889) entitled: Therapeutic Epigenetic Enhancement of the Innate Immunity to Effectively Combat Antimicrobial Resistance.Lisenssi
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