Pharmacological insights into gut microbiota modulation in systemic lupus erythematosus: Mechanisms, treatment strategies, and clinical implications.

IF 3.8 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Kantrol Kumar Sahu, Krishna Yadav, Madhulika Pradhan, Mukesh Sharma, Akhilesh Dubey, Sucheta, J John Kirubakaran
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引用次数: 0

Abstract

Systemic lupus erythematosus (SLE) is a complex autoimmune disease characterized by widespread inflammation and immune system dysregulation. Recent research suggests that the gut microbiota may play a role in the development of SLE by modulating immune system responses, affecting cytokine production, and altering the activity of T and B cells lymphocytes. As a result, there is a growing interest in microbiota-targeted therapies, including probiotics, dietary changes, and fecal microbiota transplantation. These methods may help restore the balance of microbes and reduce disease activity, but there are still a number of problems to solve. For example, microbiota composition varies greatly from person to person, and it is not clear how dysbiosis causes disease onset. There are also safety concerns about fecal microbiota transplantation. Experimental and clinical studies have started to shed light on the complicated ways in which microbial communities and immune function affect each other in SLE. These studies provide useful information, but their results are often inconsistent. As research continues, integrative methods like metagenomics and metabolomics may help find microbial signatures linked to disease, helping create more accurate and personalized treatments. The gut microbiome is a promising yet still developing area of research that could help us learn more about autoimmune diseases and their treatment, such as SLE. SIGNIFICANCE STATEMENT: Grasping the complex interplay between gut microbiota and systemic lupus erythematosus (SLE) has provided an avenue for therapeutic intervention. This study emphasizes the importance of gut dysbiosis in immune dysregulation, with connections between microbial translocation, molecular mimicry, and inflammatory pathways as contributing factors to the progression of SLE. This work sets the stage for novel and targeted approaches to treating SLE and improving patient outcomes by investigating microbiota-centric treatment options, such as probiotics, dietary interventions, and fecal microbiota transplantation.

系统性红斑狼疮中肠道菌群调节的药理学见解:机制、治疗策略和临床意义。
系统性红斑狼疮(SLE)是一种复杂的自身免疫性疾病,以广泛的炎症和免疫系统失调为特征。最近的研究表明,肠道微生物群可能通过调节免疫系统反应、影响细胞因子的产生以及改变T细胞和B细胞淋巴细胞的活性,在SLE的发展中发挥作用。因此,人们对针对微生物群的治疗越来越感兴趣,包括益生菌、饮食改变和粪便微生物群移植。这些方法可能有助于恢复微生物平衡,减少疾病活动,但仍有许多问题需要解决。例如,微生物群组成因人而异,而且尚不清楚生态失调如何导致疾病发作。还有关于粪便微生物群移植的安全问题。实验和临床研究已经开始揭示SLE中微生物群落和免疫功能相互影响的复杂方式。这些研究提供了有用的信息,但其结果往往不一致。随着研究的继续,宏基因组学和代谢组学等综合方法可能有助于发现与疾病相关的微生物特征,帮助创造更准确和个性化的治疗方法。肠道微生物组是一个很有前途但仍在发展中的研究领域,它可以帮助我们更多地了解自身免疫性疾病及其治疗,如SLE。意义声明:掌握肠道微生物群与系统性红斑狼疮(SLE)之间复杂的相互作用,为治疗干预提供了途径。本研究强调了肠道生态失调在免疫失调中的重要性,微生物易位、分子模仿和炎症途径之间的联系是SLE进展的促成因素。这项工作通过研究以微生物群为中心的治疗方案,如益生菌、饮食干预和粪便微生物群移植,为治疗SLE和改善患者预后的新方法奠定了基础。
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来源期刊
CiteScore
6.90
自引率
0.00%
发文量
115
审稿时长
1 months
期刊介绍: A leading research journal in the field of pharmacology published since 1909, JPET provides broad coverage of all aspects of the interactions of chemicals with biological systems, including autonomic, behavioral, cardiovascular, cellular, clinical, developmental, gastrointestinal, immuno-, neuro-, pulmonary, and renal pharmacology, as well as analgesics, drug abuse, metabolism and disposition, chemotherapy, and toxicology.
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