Shang Shenglan, Chen Dongxin, Wei Yuqi, Zou Shuo, Chang Qiuyue, Zhou Hong, Yu Airong
Department of Clinical Pharmacy, General Hospital of Central Theater Command, Wuhan 430070, China.
Key Laboratory of Basic Pharmacology of Ministry of Education and Joint International Research Laboratory of Ethnomedicine of Ministry of Education, Zunyi Medical University, Zunyi 563006, China.
Curr Issues Mol Biol. 2025 Jul 1;47(7):500. doi: 10.3390/cimb47070500.
Sepsis acts as the leading cause of mortality in intensive care units, characterized by life-threatening organ dysfunction due to a dysregulated host response to infection. Vitamin D (VD) pleiotropic functions were demonstrated in different biological processes, including inflammation and immunity. VD receptor (VDR) is a member of the nuclear receptor superfamily, involved in immunoregulation and resistance to infections. Previous studies have demonstrated that VD deficiency is a potential risk factor for sepsis development, which may be regulated by VDR-related physiological processes. In this review, we present a comprehensive overview of the roles of VD and VDR in sepsis, focusing on immune modulation, anti-inflammatory and anti-infective responses, oxidative stress regulation, gut microbiome enhancement, vascular endothelial cell modulation, and antiplatelet activity. We also discuss recent advances in clinical research on VD/VDR in sepsis, considering the clinical implications and potential interventions of VD analogs and VDR ligands in treatment. Despite its challenges, VD holds potential for personalized sepsis interventions. Additionally, VD/VDR may serve as a promising bidirectional immunomodulator, capable of addressing both hyperinflammatory and immunosuppressive phases of sepsis, yet require systematic investigations into its dynamic states and functions across different sepsis phases. Ongoing study and evidence-based guidelines are crucial to maximize its therapeutic benefits and improve clinical outcomes.
脓毒症是重症监护病房死亡的主要原因,其特征是宿主对感染的反应失调导致危及生命的器官功能障碍。维生素D(VD)在包括炎症和免疫在内的不同生物学过程中具有多效性功能。维生素D受体(VDR)是核受体超家族的成员,参与免疫调节和抗感染。先前的研究表明,VD缺乏是脓毒症发生的潜在危险因素,这可能受VDR相关生理过程的调节。在这篇综述中,我们全面概述了VD和VDR在脓毒症中的作用,重点关注免疫调节、抗炎和抗感染反应、氧化应激调节、肠道微生物群增强、血管内皮细胞调节和抗血小板活性。我们还讨论了脓毒症中VD/VDR临床研究的最新进展,考虑了VD类似物和VDR配体在治疗中的临床意义和潜在干预措施。尽管存在挑战,但VD在个性化脓毒症干预方面具有潜力。此外,VD/VDR可能是一种有前景的双向免疫调节剂,能够应对脓毒症的过度炎症和免疫抑制阶段,但需要对其在不同脓毒症阶段的动态状态和功能进行系统研究。持续的研究和循证指南对于最大化其治疗益处和改善临床结果至关重要。