类风湿关节炎的差异基因表达:在诊断和个体化治疗计划中的意义。

Journal of biotechnology and biomedicine Pub Date : 2025-01-01 Epub Date: 2025-05-28 DOI:10.26502/jbb.2642-91280187
Sumanjali Reddy Kanmantha Reddy, Stefanie Au, Ananta Srivastava, Emmanuel Katsaros, Devendra K Agrawal
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引用次数: 0

摘要

类风湿性关节炎(RA)是一种慢性自身免疫性疾病,由于生物、环境和遗传因素的参与,以关节炎症和破坏为特征。由于其发病机制的起源是多因素的,导致RA发展的潜在分子机制尚不清楚。因此,了解驱动RA的因素对于开发靶向治疗和改善患者预后至关重要。由于多种基因变异与RA有关,本文探讨了不同基因表达在RA患者和不同种族人群中的作用,以及这些基因如何影响RA的易感性。这篇综述的关键结论表明,HLA共享表位等位基因和非HLA基因与RA有很强的相关性,并在RA的免疫调节、自身抗体产生、细胞因子产生和关节外表现的发展中发挥重要作用。此外,RA的基因表达在不同性别和种族人群中可能存在差异,这强调了开发个性化治疗干预措施的重要性。这些发现提供了差异基因表达在改善诊断和治疗策略中的作用,并强调了RA管理的潜在治疗靶点。未来的研究需要确定差异基因表达在制定RA治疗干预措施中的临床相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Differential Gene Expression in Rheumatoid Arthritis: Implication in the Diagnosis and Individualized Treatment Plan.

Rheumatoid arthritis (RA) is a chronic autoimmune disease characterized by inflammation and destruction of the joints due to the involvement of biologic, environmental, and genetic factors. Due to its pathogenesis being multifactorial in origin, the underlying molecular mechanisms contributing to the development of RA remain unclear. Therefore, understanding the factors driving RA is crucial for developing targeted therapies and improving patient outcomes. With various genetic variants contributing to RA, this article explores the role of differential gene expression in patients with RA and in different ethnic populations and how the genes contribute to RA susceptibility. Key takeaways from this review demonstrate how HLA shared epitope alleles and non-HLA genes have a strong association with RA and play an important role in immune regulation, autoantibody production, cytokine production, and development of extra-articular manifestations observed in RA. Additionally, gene expression in RA can vary across different sexes and ethnic populations, emphasizing the importance of developing personalized therapeutic interventions. These findings provide insight into the role of differential gene expression in improving diagnostic and therapeutic strategies and highlights potential therapeutic targets for RA management. Future research is needed to determine the clinical relevance of differential gene expression in developing interventions for RA treatment.

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