Suppr超能文献

利用纳米胶囊包裹的转录激活样效应因子核酸酶(TALEN)蛋白切除人类原代细胞中的HIV-1前病毒

Excision of HIV-1 Provirus in Human Primary Cells with Nanocapsuled TALEN Proteins.

作者信息

Zhao Ming, Wen Jing, Chen Irvin S Y, Liu Jia, Lu Yunfeng

机构信息

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.

出版信息

ACS Appl Bio Mater. 2025 Feb 17;8(2):1227-1239. doi: 10.1021/acsabm.4c01544. Epub 2025 Jan 31.

Abstract

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.

摘要

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。

相似文献

1
Excision of HIV-1 Provirus in Human Primary Cells with Nanocapsuled TALEN Proteins.
ACS Appl Bio Mater. 2025 Feb 17;8(2):1227-1239. doi: 10.1021/acsabm.4c01544. Epub 2025 Jan 31.
2
4
5
Procyanidin trimer C1 derived from Theobroma cacao reactivates latent human immunodeficiency virus type 1 provirus.
Biochem Biophys Res Commun. 2015 Apr 3;459(2):288-293. doi: 10.1016/j.bbrc.2015.02.102. Epub 2015 Feb 26.
6
CRISPR/Cas9 Ablation of Integrated HIV-1 Accumulates Proviral DNA Circles with Reformed Long Terminal Repeats.
J Virol. 2021 Nov 9;95(23):e0135821. doi: 10.1128/JVI.01358-21. Epub 2021 Sep 22.
7
Stimulating the RIG-I pathway to kill cells in the latent HIV reservoir following viral reactivation.
Nat Med. 2016 Jul;22(7):807-11. doi: 10.1038/nm.4124. Epub 2016 Jun 13.
8
Synergistic reactivation of latent HIV-1 provirus by PKA activator dibutyryl-cAMP in combination with an HDAC inhibitor.
Virus Res. 2017 Jan 2;227:1-5. doi: 10.1016/j.virusres.2016.09.015. Epub 2016 Sep 24.
10
Reactivation of latent HIV-1 provirus via targeting protein phosphatase-1.
Retrovirology. 2015 Jul 16;12:63. doi: 10.1186/s12977-015-0190-4.

本文引用的文献

1
Self-adjuvanting polymeric nanovaccines enhance IFN production and cytotoxic T cell response.
J Control Release. 2024 May;369:556-572. doi: 10.1016/j.jconrel.2024.04.005. Epub 2024 Apr 10.
2
Multistage-Responsive Dual-Enzyme Nanocascades for Synergistic Radiosensitization-Starvation Cancer Therapy.
Adv Healthc Mater. 2023 Aug;12(21):e2300118. doi: 10.1002/adhm.202300118. Epub 2023 May 10.
3
In vivo engineered B cells secrete high titers of broadly neutralizing anti-HIV antibodies in mice.
Nat Biotechnol. 2022 Aug;40(8):1241-1249. doi: 10.1038/s41587-022-01328-9. Epub 2022 Jun 9.
4
Deep Sequencing Analysis of Individual HIV-1 Proviruses Reveals Frequent Asymmetric Long Terminal Repeats.
J Virol. 2022 Jul 13;96(13):e0012222. doi: 10.1128/jvi.00122-22. Epub 2022 Jun 8.
5
Pre-existing adaptive immunity to the RNA-editing enzyme Cas13d in humans.
Nat Med. 2022 Jul;28(7):1372-1376. doi: 10.1038/s41591-022-01848-6. Epub 2022 Jun 6.
6
A functional map of HIV-host interactions in primary human T cells.
Nat Commun. 2022 Apr 1;13(1):1752. doi: 10.1038/s41467-022-29346-w.
7
CRISPR-Cas9-mediated gene disruption of HIV-1 co-receptors confers broad resistance to infection in human T cells and humanized mice.
Mol Ther Methods Clin Dev. 2022 Jan 22;24:321-331. doi: 10.1016/j.omtm.2022.01.012. eCollection 2022 Mar 10.
8
Targeting CCR5 as a Component of an HIV-1 Therapeutic Strategy.
Front Immunol. 2022 Jan 20;12:816515. doi: 10.3389/fimmu.2021.816515. eCollection 2021.
10
CRISPR-Cas9 Mediated Exonic Disruption for HIV-1 Elimination.
EBioMedicine. 2021 Nov;73:103678. doi: 10.1016/j.ebiom.2021.103678. Epub 2021 Nov 10.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验