淋巴瘤发生中的HIV蓄水池:病毒抑制时代的隐藏驱动力?

IF 7.8 1区 生物学 Q1 MICROBIOLOGY
Yaoguang Li, Qing Xiao, Fengting Yu, Fujie Zhang
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引用次数: 0

摘要

尽管抗逆转录病毒治疗取得了进展,但艾滋病毒感染者(PLWH)仍然处于淋巴瘤的高风险中。HIV储存库的持续存在及其与淋巴瘤的空间关联突出了阐明其在淋巴瘤发生中的作用的必要性。HIV病毒库在感染早期建立,并通过克隆扩增、表观遗传沉默和免疫逃避来维持,可能通过四种相互关联的机制促进淋巴瘤的发生:前病毒整合效应、病毒蛋白介导的干扰、微环境失调和库再激活。目前同时针对HIV储存库和淋巴瘤的治疗方法-包括异体造血干细胞移植,嵌合抗原受体t细胞治疗和免疫检查点抑制剂-显示出希望,但面临重大挑战。迫切需要制定既能根除艾滋病毒库又能减轻淋巴瘤风险的可获得战略。这些努力可能最终使PLWH合并淋巴瘤的“双重治愈”成为可能,为对抗这种危及生命的合并症提供了新的希望。这篇综述总结了HIV储存器和HIV相关淋巴瘤之间的潜在联系,并概述了实现双重治愈的新兴治疗途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
HIV reservoirs in lymphomagenesis: hidden driver in the era of viral suppression?

SUMMARYDespite advancements in antiretroviral therapy, people living with HIV (PLWH) remain at high risk of lymphoma. The persistence of HIV reservoirs and their spatial association with lymphoma highlights the need to clarify their role in lymphomagenesis. HIV reservoirs, which are established early during infection and maintained through clonal expansion, epigenetic silencing, and immune evasion, may contribute to lymphomagenesis through four interconnected mechanisms: provirus integration effects, viral protein-mediated disturbances, microenvironment dysregulation, and reservoir reactivation. Current therapeutic approaches that simultaneously target HIV reservoirs and lymphoma-including allogeneic hematopoietic stem cell transplantation, chimeric antigen receptor T-cell therapy, and immune checkpoint inhibitors-show promise but face substantial challenges. There is an urgent need to develop accessible strategies that can both eradicate HIV reservoirs and mitigate lymphoma risk. Such efforts may ultimately enable a "double cure" for PLWH with lymphoma, offering new hope against this life-threatening comorbidity. This review summarizes the potential links between HIV reservoirs and HIV-associated lymphoma and outlines emerging therapeutic avenues toward achieving a double cure.

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来源期刊
CiteScore
18.80
自引率
0.80%
发文量
27
期刊介绍: Microbiology and Molecular Biology Reviews (MMBR), a journal that explores the significance and interrelationships of recent discoveries in various microbiology fields, publishes review articles that help both specialists and nonspecialists understand and apply the latest findings in their own research. MMBR covers a wide range of topics in microbiology, including microbial ecology, evolution, parasitology, biotechnology, and immunology. The journal caters to scientists with diverse interests in all areas of microbial science and encompasses viruses, bacteria, archaea, fungi, unicellular eukaryotes, and microbial parasites. MMBR primarily publishes authoritative and critical reviews that push the boundaries of knowledge, appealing to both specialists and generalists. The journal often includes descriptive figures and tables to enhance understanding. Indexed/Abstracted in various databases such as Agricola, BIOSIS Previews, CAB Abstracts, Cambridge Scientific Abstracts, Chemical Abstracts Service, Current Contents- Life Sciences, EMBASE, Food Science and Technology Abstracts, Illustrata, MEDLINE, Science Citation Index Expanded (Web of Science), Summon, and Scopus, among others.
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