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Immunomodulatory Effects of Non-Thermal Plasma in a Model for Latent HIV-1 Infection: Implications for an HIV-1-Specific Immunotherapy
Journal article   Open access   Peer reviewed

Immunomodulatory Effects of Non-Thermal Plasma in a Model for Latent HIV-1 Infection: Implications for an HIV-1-Specific Immunotherapy

Hager Mohamed, Rachel Berman, Jennifer Connors, Elias K Haddad, Vandana Miller, Michael R Nonnemacher, Will Dampier, Brian Wigdahl and Fred C Krebs
Biomedicines, v 11(1)
03 Jan 2023
PMID: 36672628
url
https://www.mdpi.com/2227-9059/11/1/122/pdf?version=1672750322View
Published, Version of Record (VoR) Open
url
https://doi.org/10.3390/biomedicines11010122View
Published, Version of Record (VoR) Open

Abstract

HIV-1 immunomodulation latency low temperature plasma (LTP) reactivation people living with HIV (PLWH) non-thermal plasma (NTP) chemotaxis
In people living with HIV-1 (PLWH), antiretroviral therapy (ART) eventually becomes necessary to suppress the emergence of human immunodeficiency virus type 1 (HIV-1) replication from latent reservoirs because HIV-1-specific immune responses in PLWH are suboptimal. Immunotherapies that enhance anti-HIV-1 immune responses for better control of virus reemergence from latent reservoirs are postulated to offer ART-free control of HIV-1. Toward the goal of developing an HIV-1-specific immunotherapy based on non-thermal plasma (NTP), the early immunological responses to NTP-exposed latently infected T lymphocytes were examined. Application of NTP to the J-Lat T-lymphocyte cell line (clones 10.6 and 15.4) stimulated monocyte recruitment and macrophage maturation, which are key steps in initiation of an immune response. In contrast, CD8+ T lymphocytes in a mixed lymphocyte reaction assay were not stimulated by the presence of NTP-exposed J-Lat cells. Furthermore, co-culture of NTP-exposed J-Lat cells with mature phagocytes did not modulate their antigen presentation to primary CD8+ T lymphocytes (cross-presentation). However, reactivation from latency was stimulated in a clone-specific manner by NTP. Overall, these studies, which demonstrated that ex vivo application of NTP to latently infected lymphocytes can stimulate key immune cell responses, advance the development of an NTP-based immunotherapy that will provide ART-free control of HIV-1 reactivation in PLWH.

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Web of Science research areas
Biochemistry & Molecular Biology
Medicine, Research & Experimental
Pharmacology & Pharmacy
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