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Targeting NK Cells for HIV-1 Treatment and Reservoir Clearance

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...

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Detalles Bibliográficos
Autores principales: Duan, Siqin, Liu, Shuwen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8967654/
https://www.ncbi.nlm.nih.gov/pubmed/35371060
http://dx.doi.org/10.3389/fimmu.2022.842746
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author Duan, Siqin
Liu, Shuwen
author_facet Duan, Siqin
Liu, Shuwen
author_sort Duan, Siqin
collection PubMed
description 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.
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spelling pubmed-89676542022-03-31 Targeting NK Cells for HIV-1 Treatment and Reservoir Clearance Duan, Siqin Liu, Shuwen Front Immunol Immunology 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. Frontiers Media S.A. 2022-03-16 /pmc/articles/PMC8967654/ /pubmed/35371060 http://dx.doi.org/10.3389/fimmu.2022.842746 Text en Copyright © 2022 Duan and Liu https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Duan, Siqin
Liu, Shuwen
Targeting NK Cells for HIV-1 Treatment and Reservoir Clearance
title Targeting NK Cells for HIV-1 Treatment and Reservoir Clearance
title_full Targeting NK Cells for HIV-1 Treatment and Reservoir Clearance
title_fullStr Targeting NK Cells for HIV-1 Treatment and Reservoir Clearance
title_full_unstemmed Targeting NK Cells for HIV-1 Treatment and Reservoir Clearance
title_short Targeting NK Cells for HIV-1 Treatment and Reservoir Clearance
title_sort targeting nk cells for hiv-1 treatment and reservoir clearance
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8967654/
https://www.ncbi.nlm.nih.gov/pubmed/35371060
http://dx.doi.org/10.3389/fimmu.2022.842746
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