Reddy Sumanjali Reddy Kanmantha, Au Stefanie, Srivastava Ananta, Katsaros Emmanuel, Agrawal Devendra K
Departments of Translational Research and Internal Medicine, Western University of Health Sciences, Pomona, California 91766 USA.
College of Osteopathic Medicine of the Pacific, Western University of Health Sciences, Pomona, California 91766 USA.
J Biotechnol Biomed. 2025;8(2):148-158. doi: 10.26502/jbb.2642-91280187. Epub 2025 May 28.
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.
类风湿性关节炎(RA)是一种慢性自身免疫性疾病,其特征是由于生物、环境和遗传因素的参与,导致关节发生炎症和破坏。由于其发病机制起源于多因素,导致RA发生发展的潜在分子机制仍不清楚。因此,了解驱动RA的因素对于开发靶向治疗方法和改善患者预后至关重要。鉴于多种基因变异与RA相关,本文探讨了差异基因表达在RA患者及不同种族人群中的作用,以及这些基因如何导致RA易感性。这篇综述的关键要点表明,HLA共享表位等位基因和非HLA基因如何与RA密切相关,并在免疫调节、自身抗体产生、细胞因子产生以及RA中观察到的关节外表现的发展中发挥重要作用。此外,RA中的基因表达在不同性别和种族人群中可能会有所不同,这突出了开发个性化治疗干预措施的重要性。这些发现为差异基因表达在改善诊断和治疗策略中的作用提供了见解,并突出了RA管理的潜在治疗靶点。未来需要开展研究以确定差异基因表达在开发RA治疗干预措施中的临床相关性。