Nanocarrier-enabled Gene and Nucleic Acid Therapeutics for Rheumatoid Arthritis: Advances, Translational Evidence, and Regulatory Challenges.

IF 1.5 Q4 PHARMACOLOGY & PHARMACY
Sai Geetha Meka, Sarfaroz Shaik A, Vandana Dasari, Omer Abdlgader Ibrahim Ali, Yamini Yeddhu, Nimitha Kuragala, Venu Gudisinti, Bhargav E
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引用次数: 0

Abstract

Rheumatoid arthritis (RA) is a chronic autoimmune disorder characterized by persistent synovial inflammation, cartilage degradation, and bone erosion. Conventional diseasemodifying antirheumatic drugs and biologics, although effective in many patients, are limited by systemic toxicity, variable responsiveness, and loss of efficacy over time. Recent advances in nanomedicine have enabled the development of non-viral and viral gene delivery platforms designed to modulate pathogenic pathways at the molecular level. Non-viral nanocarriers, including liposomes, polymeric nanoparticles, lipid nanoparticles, and hybrid systems, have demonstrated efficient delivery of siRNA, antisense oligonucleotides, and mRNA targeting key inflammatory mediators such as TNF-α and NF-κB, resulting in significant disease attenuation in preclinical RA models. Viral vectors, particularly adeno-associated viruses and lentiviruses, provide sustained intra-articular gene expression but raise concerns related to immunogenicity and long-term safety. Emerging gene-editing strategies, notably CRISPR/Cas-based approaches, offer the potential to precisely and durably modulate disease-driving genes. But clinical translation is restricted by off-target effects, ethical considerations, and regulatory barriers. Collectively, the available evidence underscores both the therapeutic potential and inherent complexity of nanocarrier-mediated gene and nucleic acid therapies for RA, emphasizing the necessity for optimized delivery strategies, rigorous safety assessments, and biomarker-guided patient stratification to achieve successful clinical translation. This review comprehensively covered various gene delivery modalities, including non-viral and viral vectors, and gene editing (CRISPR/Cas) approaches. At the end, preclinical and clinical evidence, along with extensive case studies, for RA treatment were also highlighted. This review also outlined challenges and future directions in the management of arthritis.

类风湿性关节炎的纳米载体基因和核酸疗法:进展、转化证据和监管挑战。
类风湿性关节炎(RA)是一种慢性自身免疫性疾病,以持续滑膜炎症、软骨退化和骨侵蚀为特征。传统的疾病改善抗风湿药物和生物制剂虽然对许多患者有效,但受到全身毒性、可变反应性和随时间丧失疗效的限制。纳米医学的最新进展使非病毒和病毒基因传递平台的发展成为可能,这些平台旨在在分子水平上调节致病途径。非病毒纳米载体,包括脂质体、聚合纳米颗粒、脂质纳米颗粒和混合系统,已经证明可以有效地递送siRNA、反义寡核苷酸和靶向关键炎症介质(如TNF-α和NF-κB)的mRNA,从而在临床前RA模型中显著减轻疾病。病毒载体,特别是腺相关病毒和慢病毒,提供持续的关节内基因表达,但引起了与免疫原性和长期安全性相关的担忧。新兴的基因编辑策略,特别是基于CRISPR/ cas的方法,提供了精确和持久地调节疾病驱动基因的潜力。但临床翻译受到脱靶效应、伦理考虑和监管障碍的限制。总的来说,现有的证据强调了纳米载体介导的基因和核酸治疗RA的治疗潜力和固有的复杂性,强调了优化递送策略、严格的安全性评估和生物标志物引导的患者分层的必要性,以实现成功的临床转化。这篇综述全面涵盖了各种基因传递方式,包括非病毒和病毒载体,以及基因编辑(CRISPR/Cas)方法。最后,还强调了类风湿关节炎治疗的临床前和临床证据以及广泛的病例研究。这篇综述还概述了关节炎治疗的挑战和未来方向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
4.30
自引率
0.00%
发文量
33
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