NLRP3炎性体在复发性妊娠丢失中的调控机制及药物治疗:研究现状与展望。

IF 4.1 2区 医学 Q2 IMMUNOLOGY
Journal of Inflammation Research Pub Date : 2025-09-06 eCollection Date: 2025-01-01 DOI:10.2147/JIR.S549048
Yonghan Cui, Yuqi Yang, Yuru Li, Yuwei Zhang, Dingren Niu, Xiaoling Feng
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引用次数: 0

摘要

复发性妊娠丢失(RPL)是一种令人痛苦的生殖系统疾病,其潜在原因复杂,治疗困难,使其成为育龄妇女普遍面临的生育挑战。近年来,炎性小体在RPL中的作用逐渐被认识到。nod样受体家族pyrin domain-containing 3 (NLRP3)是先天免疫系统的关键组成部分,也是炎症信号的中枢调节因子。越来越多的证据表明NLRP3炎性体的激活与女性生殖有关。在妊娠期间,NLRP3炎症小体的组装和激活产生促炎细胞因子和热亡相关因子,这些因子与其他炎症途径进行广泛的交叉对话,从而通过多种机制促进RPL,包括炎症级联反应、子宫内膜容受性、免疫细胞分化和极化、热亡细胞死亡、自噬和肠屏障通透性。详细了解这些复杂的相互作用可能会揭示新的治疗靶点和策略,以减轻RPL对受影响夫妇的生理和心理负担。然而,目前针对NLRP3的RPL治疗药物仍然有限。开发精确靶向和调控NLRP3的药物有望推动RPL治疗研究的发展。这篇综述研究了NLRP3炎性体和RPL之间的复杂关系,强调了炎症在疾病进展中的核心作用。总结了靶向NLRP3炎性体治疗RPL的潜在药物,为寻找临床潜在治疗靶点提供理论依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Regulatory Mechanism and Drug Therapy of NLRP3 Inflammasome in Recurrent Pregnancy Loss: Research Status and Prospect.

Regulatory Mechanism and Drug Therapy of NLRP3 Inflammasome in Recurrent Pregnancy Loss: Research Status and Prospect.

Regulatory Mechanism and Drug Therapy of NLRP3 Inflammasome in Recurrent Pregnancy Loss: Research Status and Prospect.

Recurrent pregnancy loss (RPL) is a distressing reproductive system disease with complex underlying causes and difficult treatment, making it a common fertility challenge for women of childbearing age. In recent years, the role of inflammasomes in RPL has gradually been recognized. NOD-like receptor family pyrin domain-containing 3 (NLRP3) is a key component of the innate immune system and a central regulator of inflammatory signaling. Accumulating evidence links NLRP3 inflammasome activation to female reproduction. During pregnancy, the assembly and activation of the NLRP3 inflammasome generate pro-inflammatory cytokines and pyroptosis-associated factors that engage in extensive cross-talk with other inflammatory pathways, thereby contributing to RPL through diverse mechanisms, including inflammatory cascades, endometrial receptivity, immune cell differentiation and polarization, pyroptotic cell death, autophagy, and intestinal barrier permeability. A detailed understanding of these intricate interactions may unveil novel therapeutic targets and strategies to mitigate the physiological and psychological burden of RPL on affected couples. However, currently there are still limited RPL therapeutic drugs targeting NLRP3. Developing drugs that precisely target and regulate NLRP3 is expected to promote the development of RPL therapy research. This comprehensive review investigates the complex relationship between NLRP3 inflammasome and RPL, highlighting the central role of inflammation in disease progression. It also summarizes potential drugs targeting NLRP3 inflammasome for the treatment of RPL, providing theoretical basis for potential clinical therapeutic targets.

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来源期刊
Journal of Inflammation Research
Journal of Inflammation Research Immunology and Microbiology-Immunology
CiteScore
6.10
自引率
2.20%
发文量
658
审稿时长
16 weeks
期刊介绍: An international, peer-reviewed, open access, online journal that welcomes laboratory and clinical findings on the molecular basis, cell biology and pharmacology of inflammation.
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