Department of Dermatology, Keck School of Medicine, University of Southern California, Los Angeles, CA, United States.
Department of Molecular Biology, Faculty of Biology, University of Gdańsk, Gdańsk, Poland.
Front Immunol. 2022 Dec 15;13:1080786. doi: 10.3389/fimmu.2022.1080786. eCollection 2022.
Heat shock proteins (Hsps), including Hsp90 and Hsp70, are intra- and extracellular molecules implicated in cellular homeostasis and immune processes and are induced by cell stress such as inflammation and infection. Autoimmune bullous disorders (AIBDs) and COVID-19 represent potentially life-threatening inflammatory and infectious diseases, respectively. A significant portion of AIBDs remain refractory to currently available immunosuppressive therapies, which may represent a risk factor for COVID-19, and suffer from treatment side-effects. Despite advances in vaccination, there is still a need to develop new therapeutic approaches targeting SARS-CoV-2, especially considering vaccine hesitancy, logistical distribution challenges, and breakthrough infections. In this mini review, we briefly summarize the role of targeting Hsp90/70 as a promising double-edged sword in the therapy of AIBDs and COVID-19.
热休克蛋白(Hsps),包括 Hsp90 和 Hsp70,是细胞内和细胞外的分子,参与细胞内环境稳定和免疫过程,并受到炎症和感染等细胞应激的诱导。自身免疫性大疱性疾病(AIBDs)和 COVID-19 分别代表潜在危及生命的炎症性和传染性疾病。很大一部分 AIBDs 仍然对目前可用的免疫抑制治疗无反应,这可能是 COVID-19 的一个危险因素,并伴有治疗副作用。尽管在疫苗接种方面取得了进展,但仍需要开发针对 SARS-CoV-2 的新治疗方法,特别是考虑到疫苗犹豫、物流配送挑战和突破性感染。在这个小型综述中,我们简要总结了靶向 Hsp90/70 的作用,将其作为治疗 AIBDs 和 COVID-19 的一种有前途的双刃剑。