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突破治愈HIV-1的障碍:基因编辑、免疫调节和病毒储存库清除方面的创新

Breaking Barriers to an HIV-1 Cure: Innovations in Gene Editing, Immune Modulation, and Reservoir Eradication.

作者信息

Borrajo Ana

机构信息

Department of Microbiology and Parasitology, Faculty of Pharmacy, Complutense University of Madrid, 28040 Madrid, Spain.

出版信息

Life (Basel). 2025 Feb 11;15(2):276. doi: 10.3390/life15020276.

Abstract

Recent advances in virology, particularly in the study of HIV-1, have significantly progressed the pursuit of a definitive cure for the disease. Emerging therapeutic strategies encompass innovative gene-editing technologies, immune-modulatory interventions, and next-generation antiretroviral agents. Efforts to eliminate or control viral reservoirs have also gained momentum, with the aim of achieving durable viral remission without the continuous requirement for antiretroviral therapy. Despite these promising developments, critical challenges persist in bridging the gap between laboratory findings and clinical implementation. This review provides a comprehensive analysis of recent breakthroughs, ongoing clinical trials, and the barriers that must be addressed to translate these advancements into effective treatments, emphasizing the multifaceted approaches being pursued to achieve a curative solution for HIV-1 infection.

摘要

病毒学领域的最新进展,尤其是在HIV-1研究方面,已极大地推动了对该疾病彻底治愈方法的探索。新兴的治疗策略包括创新的基因编辑技术、免疫调节干预措施以及新一代抗逆转录病毒药物。消除或控制病毒储存库的努力也在加速推进,目标是在无需持续进行抗逆转录病毒治疗的情况下实现持久的病毒缓解。尽管取得了这些令人鼓舞的进展,但在弥合实验室研究结果与临床应用之间的差距方面,仍存在重大挑战。本综述全面分析了近期的突破、正在进行的临床试验以及将这些进展转化为有效治疗方法时必须克服的障碍,强调了为实现HIV-1感染的治愈方案而采用的多方面方法。

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