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免疫检查点是调节心脑血管疾病和CD4Foxp3调节性T细胞免疫抑制的新治疗靶点。

Immune Checkpoints Are New Therapeutic Targets in Regulating Cardio-, and Cerebro-Vascular Diseases and CD4Foxp3 Regulatory T Cell Immunosuppression.

作者信息

Shao Ying, Yang William Y, Nanayakkara Gayani, Saaoud Fatma, Ben Issa Mohammed, Xu Keman, Lu Yifan, Jiang Xiaohua, Mohsin Sadia, Wang Hong, Yang Xiaofeng

机构信息

Lemole Center for Integrated Lymphatics and Vascular Research, Department of Cardiovascular Sciences, Lewis Katz School of Medicine at Temple University, Philadelphia, PA19140, USA.

Center for Metabolic Disease Research, Department of Cardiovascular Sciences, Lewis Katz School of Medicine at Temple University, Philadelphia, PA19140, USA.

出版信息

Int J Drug Discov Pharm. 2024 Dec;3(4). doi: 10.53941/ijddp.2024.100022. Epub 2024 Nov 26.

Abstract

Although previous reviews explored the roles of selected immune checkpoints (ICPs) in cardiovascular diseases (CVD) and cerebrovascular diseases from various perspectives, many related aspects have yet to be thoroughly reviewed and analyzed. Our comprehensive review addresses this gap by discussing the cellular functions of ICPs, focusing on the tissue-specific and microenvironment-localized transcriptomic and posttranslational regulation of ICP expressions, as well as their functional interactions with metabolic reprogramming. We also analyze how 14 pairs of ICPs, including CTLA-4/CD86-CD80, PD1-PDL-1, and TIGIT-CD155, regulate CVD pathogenesis. Additionally, the review covers the roles of ICPs in modulating CD4Foxp3 regulatory T cells (Tregs), T cells, and innate immune cells in various CVDs and cerebrovascular diseases. Furthermore, we outline seven immunological principles to guide the development of new ICP-based therapies for CVDs. This timely and thorough analysis of recent advancements and challenges provide new insights into the role of ICPs in CVDs, cerebrovascular diseases and Tregs, and will support the development of novel therapeutics strategies for these diseases.

摘要

尽管先前的综述从各种角度探讨了特定免疫检查点(ICP)在心血管疾病(CVD)和脑血管疾病中的作用,但许多相关方面仍有待全面综述和分析。我们的综合综述通过讨论ICP的细胞功能来填补这一空白,重点关注ICP表达的组织特异性和微环境定位的转录组学及翻译后调控,以及它们与代谢重编程的功能相互作用。我们还分析了包括CTLA-4/CD86-CD80、PD1-PDL-1和TIGIT-CD155在内的14对ICP如何调节CVD发病机制。此外,该综述涵盖了ICP在各种CVD和脑血管疾病中调节CD4Foxp3调节性T细胞(Tregs)、T细胞和先天免疫细胞的作用。此外,我们概述了七条免疫学原则,以指导基于ICP的CVD新疗法的开发。对近期进展和挑战的及时而全面的分析为ICP在CVD、脑血管疾病和Tregs中的作用提供了新的见解,并将支持这些疾病新治疗策略的开发。

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