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针对 HIV-1 的治疗和清除储存库的 NK 细胞。

Targeting NK Cells for HIV-1 Treatment and Reservoir Clearance.

机构信息

Department of Clinical Laboratory, Guangzhou Women and Children Medical Center, Guangzhou Medical University, Guangzhou, China.

Guangdong Provincial Key Laboratory of New Drug Screening, School of Pharmaceutical Sciences, Southern Medical University, Guangzhou, China.

出版信息

Front Immunol. 2022 Mar 16;13:842746. doi: 10.3389/fimmu.2022.842746. eCollection 2022.


DOI:10.3389/fimmu.2022.842746
PMID:35371060
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8967654/
Abstract

Combined antiretroviral therapy (cART) can inhibit the replication of human immunodeficiency virus type 1 (HIV-1) and reduce viral loads in the peripheral blood to undetectable levels. However, the presence of latent HIV-1 reservoirs prevents complete HIV-1 eradication. Several drugs and strategies targeting T cells are now in clinical trials, but their effectiveness in reducing viral reservoirs has been mixed. Interestingly, innate immune natural killer (NK) cells, which are promising targets for cancer therapy, also play an important role in HIV-1 infection. NK cells are a unique innate cell population with features of adaptive immunity that can regulate adaptive and innate immune cell populations; therefore, they can be exploited for HIV-1 immunotherapy and reservoir eradication. In this review, we highlight immunotherapy strategies for HIV infection that utilize the beneficial properties of NK cells.

摘要

联合抗逆转录病毒疗法(cART)可抑制人类免疫缺陷病毒 1 型(HIV-1)的复制,并将外周血中的病毒载量降低至无法检测的水平。然而,潜伏的 HIV-1 储库的存在阻止了 HIV-1 的完全清除。目前有几种针对 T 细胞的药物和策略正在临床试验中,但它们在减少病毒储库方面的效果参差不齐。有趣的是,先天免疫自然杀伤(NK)细胞,作为癌症治疗的有前途的靶点,在 HIV-1 感染中也发挥着重要作用。NK 细胞是一种具有适应性免疫特征的独特先天细胞群体,可调节适应性和先天免疫细胞群体;因此,它们可被用于 HIV-1 免疫治疗和储库清除。在这篇综述中,我们强调了利用 NK 细胞有益特性的 HIV 感染免疫治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fd9/8967654/2fa3f8e892c7/fimmu-13-842746-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fd9/8967654/fd6550ccf4fb/fimmu-13-842746-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fd9/8967654/2fa3f8e892c7/fimmu-13-842746-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fd9/8967654/fd6550ccf4fb/fimmu-13-842746-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fd9/8967654/2fa3f8e892c7/fimmu-13-842746-g002.jpg

相似文献

[1]
Targeting NK Cells for HIV-1 Treatment and Reservoir Clearance.

Front Immunol. 2022

[2]
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J Virol. 2021-8-10

[3]
Interleukin-15-Stimulated Natural Killer Cells Clear HIV-1-Infected Cells following Latency Reversal .

J Virol. 2018-5-29

[4]
Innate Immune Activity Correlates with CD4 T Cell-Associated HIV-1 DNA Decline during Latency-Reversing Treatment with Panobinostat.

J Virol. 2015-10

[5]
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J Virol. 2017-11-14

[6]
KLRG1 expression on natural killer cells is associated with HIV persistence, and its targeting promotes the reduction of the viral reservoir.

Cell Rep Med. 2023-10-17

[7]
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J Virol. 2016-4-14

[8]
Reservoirs for HIV-1: mechanisms for viral persistence in the presence of antiviral immune responses and antiretroviral therapy.

Annu Rev Immunol. 2000

[9]
Potential of the NKG2D/NKG2DL Axis in NK Cell-Mediated Clearance of the HIV-1 Reservoir.

Int J Mol Sci. 2019-9-11

[10]
Combination of CD8β Depletion and Interleukin-15 Superagonist N-803 Induces Virus Reactivation in Simian-Human Immunodeficiency Virus-Infected, Long-Term ART-Treated Rhesus Macaques.

J Virol. 2020-9-15

引用本文的文献

[1]
[Immunological Causes of Oral Manifestations of HIV Infection: A Literature Review].

Rev Cient Odontol (Lima). 2025-5-16

[2]
Afucosylated broadly neutralizing antibodies enhance clearance of HIV-1 infected cells through cell-mediated killing.

Commun Biol. 2024-8-9

[3]
HIV Persistence, Latency, and Cure Approaches: Where Are We Now?

Viruses. 2024-7-19

[4]
Editorial: Forty Years of Waiting for Prevention and Cure of HIV Infection - Ongoing Challenges and Hopes for Vaccine Development and Overcoming Antiretroviral Drug Resistance.

Med Sci Monit. 2024-4-1

[5]
Innate lymphoid cells-Underexplored guardians of immunity.

PLoS Pathog. 2023-10-19

[6]
Natural killer cells and their exosomes in viral infections and related therapeutic approaches: where are we?

Cell Commun Signal. 2023-9-25

本文引用的文献

[1]
Changes in NK Cell Subsets and Receptor Expressions in HIV-1 Infected Chronic Patients and HIV Controllers.

Front Immunol. 2021

[2]
A Genome-Wide CRISPR/Cas9-Based Screen Identifies Heparan Sulfate Proteoglycans as Ligands of Killer-Cell Immunoglobulin-Like Receptors.

Front Immunol. 2021

[3]
Exhausted NK cells and cytokine storms in COVID-19: Whether NK cell therapy could be a therapeutic choice.

Hum Immunol. 2022-1

[4]
The role of natural killer cells in liver inflammation.

Semin Immunopathol. 2021-8

[5]
Oncolytic parainfluenza virus combines with NK cells to mediate killing of infected and non-infected lung cancer cells within 3D spheroids: role of type I and type III interferon signaling.

J Immunother Cancer. 2021-6

[6]
CD276 expression enables squamous cell carcinoma stem cells to evade immune surveillance.

Cell Stem Cell. 2021-9-2

[7]
NK cell-based cancer immunotherapy: from basic biology to clinical development.

J Hematol Oncol. 2021-1-6

[8]
TRIGGERED: could refocused cell signaling be key to natural killer cell-based HIV immunotherapeutics?

AIDS. 2021-2-2

[9]
Exploring the NK cell platform for cancer immunotherapy.

Nat Rev Clin Oncol. 2021-2

[10]
Harnessing Natural Killer Cell Innate and Adaptive Traits in HIV Infection.

Front Cell Infect Microbiol. 2020-8-4

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