Abstract

In recent years, RNA-based therapeutics have emerged as a groundbreaking field, offering innovative approaches for drug development and therapeutic interventions. This review article presents a comprehensive exploration of the advancements in RNA-based therapeutics, focusing on key modalities such as RNA interference (RNAi), antisense oligonucleotides (ASOs), messenger RNA (mRNA) vaccines, and other emerging RNA-based therapies. The introduction provides an insightful overview of the potential of RNA as a therapeutic target, highlighting its unique mechanisms of action and its transformative role in precision medicine. Subsequently, the review delves into the intricacies of RNAi, explaining the function of small interfering RNAs (siRNAs) and microRNAs (miRNAs) in selectively silencing disease-associated genes, thereby opening new avenues for therapeutic interventions. Antisense oligonucleotides (ASOs) are discussed in detail, elucidating how they target mRNA for degradation or modulation of splicing, offering promising solutions for treating genetic disorders, neurodegenerative diseases, and viral infections. Additionally, the groundbreaking success of mRNA vaccines is explored, with an emphasis on their role in combatting infectious diseases like COVID-19 and their potential application in cancer immunotherapy and other therapeutic areas. Addressing the critical issue of delivery challenges in RNA-based therapeutics, the review presents various strategies to enhance stability, cellular uptake, and minimize immunogenicity, thereby improving the effectiveness of these therapies in reaching their intended targets. Clinical successes and challenges of RNA-based therapeutics are critically evaluated, providing insights into ongoing clinical trials and approved therapies. Success stories underscore the transformative potential of RNA-based treatments, while safety concerns are addressed, paving the way for safer and more efficient therapeutic applications. The review concludes by exploring future prospects and innovations in the field, highlighting novel delivery strategies, advancements in RNA editing technologies, and the promise of combination therapies to augment therapeutic outcomes. Regulatory considerations and commercialization challenges are also discussed, offering an understanding of the regulatory landscape for RNA-based therapeutics and the potential for market growth. In conclusion, this review article serves as an informative resource for researchers, clinicians, and pharmaceutical professionals, shedding light on the rapid progress in RNA-based therapeutics and their potential to revolutionize disease treatment. By integrating knowledge from diverse sources, this review contributes to advancing the field and underscores the exciting possibilities of RNA-based interventions in improving patient outcomes and addressing unmet medical needs.

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