Zhao Ming, Wen Jing, Chen Irvin S Y, Liu Jia, Lu Yunfeng
Department of Chemical and Biomolecular Engineering, University of California, Los Angeles, Los Angeles, California 90095, United States.
Department of Microbiology, Immunology and Molecular Genetics, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, California 90095, United States.
ACS Appl Bio Mater. 2025 Feb 17;8(2):1227-1239. doi: 10.1021/acsabm.4c01544. Epub 2025 Jan 31.
Despite the tremendous success of combination antiretroviral therapy (ART) to treat human immunodeficiency virus (HIV) infection, the durability and persistence of latent reservoirs of HIV-infected cells in HIV-infected patients remain obstacles to achieving HIV cure. While technically challenging, the most direct means to eradicate latent reservoirs is to destroy the HIV provirus, thus ensuring that HIV virions are not produced while preserving resident cells. Transcription activator-like effector nucleases (TALEN)─a genome editing method with high DNA targeting efficiency─have been investigated as a potential gene therapy by disrupting the HIV-1 coreceptor CCR5 genes in HIV target cells or HIV proviral DNA in infected cells. However, the transduction and editing efficiencies are low in primary cells and vary by cell type. Using a nanotechnology platform, which we term nanocapsules, the TALEN protein can be effectively delivered into primary cells and escape from endosome/lysosome sequestration. We report that TALEN nanocapsules can effectively mutagenize the HIV-1 proviral DNA integrated into two primary HIV-1 reservoir cells─T cells and macrophages, such that replication and/or reactivation from latency is aborted. We envision that this study provides a useful platform to deliver a wide range of DNA-modifying enzymes for effective HIV therapy.
尽管联合抗逆转录病毒疗法(ART)在治疗人类免疫缺陷病毒(HIV)感染方面取得了巨大成功,但HIV感染患者体内HIV感染细胞潜伏库的持久性和持续性仍然是实现HIV治愈的障碍。虽然技术上具有挑战性,但根除潜伏库最直接的方法是破坏HIV前病毒,从而确保在保留宿主细胞的同时不产生HIV病毒颗粒。转录激活样效应核酸酶(TALEN)——一种具有高DNA靶向效率的基因组编辑方法——已被研究作为一种潜在的基因疗法,通过破坏HIV靶细胞中的HIV-1共受体CCR5基因或感染细胞中的HIV前病毒DNA来实现。然而,原代细胞中的转导和编辑效率较低,且因细胞类型而异。使用一种我们称为纳米胶囊的纳米技术平台,TALEN蛋白可以有效地递送至原代细胞,并从内体/溶酶体隔离中逃逸。我们报告称,TALEN纳米胶囊可以有效地诱变整合到两种主要HIV-1潜伏库细胞——T细胞和巨噬细胞中的HIV-1前病毒DNA,从而中止潜伏状态下的复制和/或重新激活。我们设想这项研究为有效治疗HIV提供了一个有用的平台,可用于递送多种DNA修饰酶。