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Eradication of Human Immunodeficiency Virus Type-1 (HIV-1)-Infected Cells

Predictions made soon after the introduction of human immunodeficiency virus type-1 (HIV-1) protease inhibitors about potentially eradicating the cellular reservoirs of HIV-1 in infected individuals were too optimistic. The ability of the HIV-1 genome to remain in the chromosomes of resting CD4+ T c...

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Autores principales: Düzgüneş, Nejat, Konopka, Krystyna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6631149/
https://www.ncbi.nlm.nih.gov/pubmed/31159417
http://dx.doi.org/10.3390/pharmaceutics11060255
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author Düzgüneş, Nejat
Konopka, Krystyna
author_facet Düzgüneş, Nejat
Konopka, Krystyna
author_sort Düzgüneş, Nejat
collection PubMed
description Predictions made soon after the introduction of human immunodeficiency virus type-1 (HIV-1) protease inhibitors about potentially eradicating the cellular reservoirs of HIV-1 in infected individuals were too optimistic. The ability of the HIV-1 genome to remain in the chromosomes of resting CD4+ T cells and macrophages without being expressed (HIV-1 latency) has prompted studies to activate the cells in the hopes that the immune system can recognize and clear these cells. The absence of natural clearance of latently infected cells has led to the recognition that additional interventions are necessary. Here, we review the potential of utilizing suicide gene therapy to kill infected cells, excising the chromosome-integrated HIV-1 DNA, and targeting cytotoxic liposomes to latency-reversed HIV-1-infected cells.
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spelling pubmed-66311492019-08-19 Eradication of Human Immunodeficiency Virus Type-1 (HIV-1)-Infected Cells Düzgüneş, Nejat Konopka, Krystyna Pharmaceutics Review Predictions made soon after the introduction of human immunodeficiency virus type-1 (HIV-1) protease inhibitors about potentially eradicating the cellular reservoirs of HIV-1 in infected individuals were too optimistic. The ability of the HIV-1 genome to remain in the chromosomes of resting CD4+ T cells and macrophages without being expressed (HIV-1 latency) has prompted studies to activate the cells in the hopes that the immune system can recognize and clear these cells. The absence of natural clearance of latently infected cells has led to the recognition that additional interventions are necessary. Here, we review the potential of utilizing suicide gene therapy to kill infected cells, excising the chromosome-integrated HIV-1 DNA, and targeting cytotoxic liposomes to latency-reversed HIV-1-infected cells. MDPI 2019-06-01 /pmc/articles/PMC6631149/ /pubmed/31159417 http://dx.doi.org/10.3390/pharmaceutics11060255 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Düzgüneş, Nejat
Konopka, Krystyna
Eradication of Human Immunodeficiency Virus Type-1 (HIV-1)-Infected Cells
title Eradication of Human Immunodeficiency Virus Type-1 (HIV-1)-Infected Cells
title_full Eradication of Human Immunodeficiency Virus Type-1 (HIV-1)-Infected Cells
title_fullStr Eradication of Human Immunodeficiency Virus Type-1 (HIV-1)-Infected Cells
title_full_unstemmed Eradication of Human Immunodeficiency Virus Type-1 (HIV-1)-Infected Cells
title_short Eradication of Human Immunodeficiency Virus Type-1 (HIV-1)-Infected Cells
title_sort eradication of human immunodeficiency virus type-1 (hiv-1)-infected cells
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6631149/
https://www.ncbi.nlm.nih.gov/pubmed/31159417
http://dx.doi.org/10.3390/pharmaceutics11060255
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