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

Department of Biomedical Sciences, Arthur A. Dugoni School of Dentistry, University of the Pacific, 155 Fifth Street, Room 412, San Francisco, CA 94103, USA
Author to whom correspondence should be addressed.
Pharmaceutics 2019, 11(6), 255;
Received: 12 March 2019 / Revised: 1 May 2019 / Accepted: 24 May 2019 / Published: 1 June 2019
(This article belongs to the Special Issue Novel Approaches for Delivery of Anti-HIV Drugs)
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. View Full-Text
Keywords: suicide gene therapy; CRISPR/Cas9; broadly neutralizing antibodies; cytotoxic liposomes; lentivirus suicide gene therapy; CRISPR/Cas9; broadly neutralizing antibodies; cytotoxic liposomes; lentivirus
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Düzgüneş, N.; Konopka, K. Eradication of Human Immunodeficiency Virus Type-1 (HIV-1)-Infected Cells. Pharmaceutics 2019, 11, 255.

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