路障导航:人类免疫缺陷病毒细胞疗法的进展与挑战》。

IF 3 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Lakshay Chhabra, Rajeev Kumar Pandey, Rajiv Kumar, Shyam Sundar, Sanjana Mehrotra
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引用次数: 0

摘要

以细胞为基础的疗法是艾滋病治疗和管理的一大进步,其目标是克服传统抗逆转录病毒疗法(ART)的局限性。这些创新方法不仅有望通过重建免疫系统实现功能性治愈,还能解决病毒库持续存在的问题。例如,干细胞疗法是在异体造血干细胞移植成功治愈少数艾滋病感染病例的基础上发展起来的。B 细胞疗法利用基因改造的 B 细胞,针对目标病毒颗粒和受感染细胞持续表达广谱中和抗体(bNAbs)。采用性细胞转移(ACT),包括 TCR-T 疗法、CAR-T 细胞、NK-CAR 细胞和基于 DC 的疗法,是从癌症免疫疗法改良而来,并重新用于根除 HIV。在这篇综述中,我们总结了这些改造细胞识别和消灭 HIV 感染细胞的机制、改造策略及其在抗逆转录病毒疗法缺失的情况下维持缓解的作用。综述还探讨了细胞疗法在抗击 HIV 方面面临的挑战,并讨论了旨在克服这些挑战的最新进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Navigating the Roadblocks: Progress and Challenges in Cell-Based Therapies for Human Immunodeficiency Virus.

Cell-based therapies represent a major advancement in the treatment and management of HIV/AIDS, with a goal to overcome the limitations of traditional antiretroviral therapy (ART). These innovative approaches not only promise a functional cure by reconstructing the immune landscape but also address the persistent viral reservoirs. For example, stem cell therapies have emerged from the foundational success of allogeneic hematopoietic stem cell transplantation in curing HIV infection in a limited number of cases. B cell therapies make use of genetically modified B cells constitutively expressing broadly neutralizing antibodies (bNAbs) against target viral particles and infected cells. Adoptive cell transfer (ACT), including TCR-T therapy, CAR-T cells, NK-CAR cells, and DC-based therapy, is adapted from cancer immunotherapy and repurposed for HIV eradication. In this review, we summarize the mechanisms through which these engineered cells recognize and destroy HIV-infected cells, the modification strategies, and their role in sustaining remission in the absence of ART. The review also addresses the challenges to cell-based therapies against HIV and discusses the recent advancements aimed at overcoming them.

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来源期刊
Journal of cellular biochemistry
Journal of cellular biochemistry 生物-生化与分子生物学
CiteScore
9.90
自引率
0.00%
发文量
164
审稿时长
1 months
期刊介绍: The Journal of Cellular Biochemistry publishes descriptions of original research in which complex cellular, pathogenic, clinical, or animal model systems are studied by biochemical, molecular, genetic, epigenetic or quantitative ultrastructural approaches. Submission of papers reporting genomic, proteomic, bioinformatics and systems biology approaches to identify and characterize parameters of biological control in a cellular context are encouraged. The areas covered include, but are not restricted to, conditions, agents, regulatory networks, or differentiation states that influence structure, cell cycle & growth control, structure-function relationships.
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