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焦亡在银屑病和化脓性汗腺炎中的病理及治疗意义:一项叙述性综述

Pathological and Therapeutical Implications of Pyroptosis in Psoriasis and Hidradenitis Suppurativa: A Narrative Review.

作者信息

Krajewski Piotr K, Tsoukas Maria, Szepietowski Jacek C

机构信息

Department of Dermatology, Venereology and Allergology, Wroclaw Medical University, Chalubinskiego 1, 50-368 Wroclaw, Poland.

Department of Dermatology, University of Illinois at Chicago, Chicago, IL 60607, USA.

出版信息

Curr Issues Mol Biol. 2024 Jan 11;46(1):663-676. doi: 10.3390/cimb46010043.

Abstract

This manuscript explores the role of pyroptosis, an inflammatory programmed cell death, in the pathogenesis of two chronic dermatoses, psoriasis and hidradenitis suppurativa (HS). The diseases, though clinically diverse, share common pathogenetic pathways involving the unbalanced interaction between the adaptive and innate immune systems. This review focuses on the molecular changes in psoriatic and HS skin, emphasizing the activation of dendritic cells, secretion of interleukins (IL-17, IL-22, and TNF-α), and the involvement of inflammasomes, particularly NLRP3. This manuscript discusses the role of caspases, especially caspase-1, in driving pyroptosis and highlights the family of gasdermins (GSDMs) as key players in the formation of pores leading to cell rupture and the release of proinflammatory signals. This study delves into the potential therapeutic implications of targeting pyroptosis in psoriasis and HS, examining existing medications like biologics and Janus kinase inhibitors. It also reviews the current limitations and challenges in developing therapies that selectively target pyroptosis. Additionally, the manuscript explores the role of pyroptosis in various inflammatory disorders associated with psoriasis and HS, such as inflammatory bowel disease, diabetes mellitus, and cardiovascular disorders. The review concludes by emphasizing the need for further research to fully elucidate the pathomechanisms of these dermatoses and develop effective, targeted therapies.

摘要

本手稿探讨了炎性程序性细胞死亡——细胞焦亡在两种慢性皮肤病,即银屑病和化脓性汗腺炎(HS)发病机制中的作用。这两种疾病虽然临床表现各异,但具有共同的致病途径,涉及适应性免疫系统与先天性免疫系统之间的失衡相互作用。本综述重点关注银屑病和HS皮肤中的分子变化,强调树突状细胞的激活、白细胞介素(IL-17、IL-22和TNF-α)的分泌以及炎性小体的参与,尤其是NLRP3。本手稿讨论了半胱天冬酶,特别是半胱天冬酶-1在驱动细胞焦亡中的作用,并强调了gasdermin(GSDM)家族在形成导致细胞破裂和促炎信号释放的孔道中的关键作用。本研究深入探讨了针对银屑病和HS中的细胞焦亡进行治疗的潜在意义,研究了生物制剂和Janus激酶抑制剂等现有药物。它还回顾了开发选择性靶向细胞焦亡疗法目前的局限性和挑战。此外,本手稿探讨了细胞焦亡在与银屑病和HS相关的各种炎症性疾病中的作用,如炎症性肠病、糖尿病和心血管疾病。综述最后强调,需要进一步研究以充分阐明这些皮肤病的发病机制,并开发有效、有针对性的疗法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c64/10814322/b594fd274c22/cimb-46-00043-g001.jpg

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