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

Viral persistency in latently infected CD4<sup>+</sup> T cells despite antiretroviral therapy (ART) represents a major drawback in the fight against HIV-1. Efforts to purge latent HIV-1 have been attempted using latency reversing agents (LRAs) that activate expression of the quiescent vi...

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Main Authors: Maria G. Desimio, Daniela A. Covino, Margherita Doria
Format: Article
Language:English
Published: MDPI AG 2019-09-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/20/18/4490
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spelling doaj-f0d580e68b5b4187a1431b9101c4f8412020-11-25T02:03:36ZengMDPI AGInternational Journal of Molecular Sciences1422-00672019-09-012018449010.3390/ijms20184490ijms20184490Potential of the NKG2D/NKG2DL Axis in NK Cell-Mediated Clearance of the HIV-1 ReservoirMaria G. Desimio0Daniela A. Covino1Margherita Doria2Academic Department of Pediatrics, Bambino Gesù Children’s Hospital, IRCCS, 00165 Rome, ItalyAcademic Department of Pediatrics, Bambino Gesù Children’s Hospital, IRCCS, 00165 Rome, ItalyAcademic Department of Pediatrics, Bambino Gesù Children’s Hospital, IRCCS, 00165 Rome, ItalyViral persistency in latently infected CD4<sup>+</sup> T cells despite antiretroviral therapy (ART) represents a major drawback in the fight against HIV-1. Efforts to purge latent HIV-1 have been attempted using latency reversing agents (LRAs) that activate expression of the quiescent virus. However, initial trials have shown that immune responses of ART-treated patients are ineffective at clearing LRA-reactivated HIV-1 reservoirs, suggesting that an adjuvant immunotherapy is needed. Here we overview multiple lines of evidence indicating that natural killer (NK) cells have the potential to induce anti-HIV-1 responses relevant for virus eradication. In particular, we focus on the role of the NKG2D activating receptor that crucially enables NK cell-mediated killing of HIV-1-infected cells. We describe recent data indicating that LRAs can synergize with HIV-1 at upregulating ligands for NKG2D (NKG2DLs), hence sensitizing T cells that exit from viral latency for recognition and lysis by NK cells; in addition, we report in vivo and ex vivo data showing the potential benefits and drawbacks that LRAs may have on NKG2D expression and, more in general, on the cytotoxicity of NK cells. Finally, we discuss how the NKG2D/NKG2DLs axis can be exploited for the development of effective HIV-1 eradication strategies combining LRA-induced virus reactivation with recently optimized NK cell-based immunotherapies.https://www.mdpi.com/1422-0067/20/18/4490HIV-1 eradicationnatural killer (NK) cellsNKG2Dlatency reversing agentsimmunotherapy
collection DOAJ
language English
format Article
sources DOAJ
author Maria G. Desimio
Daniela A. Covino
Margherita Doria
spellingShingle Maria G. Desimio
Daniela A. Covino
Margherita Doria
Potential of the NKG2D/NKG2DL Axis in NK Cell-Mediated Clearance of the HIV-1 Reservoir
International Journal of Molecular Sciences
HIV-1 eradication
natural killer (NK) cells
NKG2D
latency reversing agents
immunotherapy
author_facet Maria G. Desimio
Daniela A. Covino
Margherita Doria
author_sort Maria G. Desimio
title Potential of the NKG2D/NKG2DL Axis in NK Cell-Mediated Clearance of the HIV-1 Reservoir
title_short Potential of the NKG2D/NKG2DL Axis in NK Cell-Mediated Clearance of the HIV-1 Reservoir
title_full Potential of the NKG2D/NKG2DL Axis in NK Cell-Mediated Clearance of the HIV-1 Reservoir
title_fullStr Potential of the NKG2D/NKG2DL Axis in NK Cell-Mediated Clearance of the HIV-1 Reservoir
title_full_unstemmed Potential of the NKG2D/NKG2DL Axis in NK Cell-Mediated Clearance of the HIV-1 Reservoir
title_sort potential of the nkg2d/nkg2dl axis in nk cell-mediated clearance of the hiv-1 reservoir
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1422-0067
publishDate 2019-09-01
description Viral persistency in latently infected CD4<sup>+</sup> T cells despite antiretroviral therapy (ART) represents a major drawback in the fight against HIV-1. Efforts to purge latent HIV-1 have been attempted using latency reversing agents (LRAs) that activate expression of the quiescent virus. However, initial trials have shown that immune responses of ART-treated patients are ineffective at clearing LRA-reactivated HIV-1 reservoirs, suggesting that an adjuvant immunotherapy is needed. Here we overview multiple lines of evidence indicating that natural killer (NK) cells have the potential to induce anti-HIV-1 responses relevant for virus eradication. In particular, we focus on the role of the NKG2D activating receptor that crucially enables NK cell-mediated killing of HIV-1-infected cells. We describe recent data indicating that LRAs can synergize with HIV-1 at upregulating ligands for NKG2D (NKG2DLs), hence sensitizing T cells that exit from viral latency for recognition and lysis by NK cells; in addition, we report in vivo and ex vivo data showing the potential benefits and drawbacks that LRAs may have on NKG2D expression and, more in general, on the cytotoxicity of NK cells. Finally, we discuss how the NKG2D/NKG2DLs axis can be exploited for the development of effective HIV-1 eradication strategies combining LRA-induced virus reactivation with recently optimized NK cell-based immunotherapies.
topic HIV-1 eradication
natural killer (NK) cells
NKG2D
latency reversing agents
immunotherapy
url https://www.mdpi.com/1422-0067/20/18/4490
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