Cargando…

Targeted Nanocarrier Delivery of RNA Therapeutics to Control HIV Infection

Our understanding of HIV infection has greatly advanced since the discovery of the virus in 1983. Treatment options have improved the quality of life of people living with HIV/AIDS, turning it from a fatal disease into a chronic, manageable infection. Despite all this progress, a cure remains elusiv...

Descripción completa

Detalles Bibliográficos
Autores principales: Agbosu, Esinam E., Ledger, Scott, Kelleher, Anthony D., Wen, Jing, Ahlenstiel, Chantelle L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9324444/
https://www.ncbi.nlm.nih.gov/pubmed/35890248
http://dx.doi.org/10.3390/pharmaceutics14071352
_version_ 1784756807987625984
author Agbosu, Esinam E.
Ledger, Scott
Kelleher, Anthony D.
Wen, Jing
Ahlenstiel, Chantelle L.
author_facet Agbosu, Esinam E.
Ledger, Scott
Kelleher, Anthony D.
Wen, Jing
Ahlenstiel, Chantelle L.
author_sort Agbosu, Esinam E.
collection PubMed
description Our understanding of HIV infection has greatly advanced since the discovery of the virus in 1983. Treatment options have improved the quality of life of people living with HIV/AIDS, turning it from a fatal disease into a chronic, manageable infection. Despite all this progress, a cure remains elusive. A major barrier to attaining an HIV cure is the presence of the latent viral reservoir, which is established early in infection and persists for the lifetime of the host, even during prolonged anti-viral therapy. Different cure strategies are currently being explored to eliminate or suppress this reservoir. Several studies have shown that a functional cure may be achieved by preventing infection and also inhibiting reactivation of the virus from the latent reservoir. Here, we briefly describe the main HIV cure strategies, focussing on the use of RNA therapeutics, including small interfering RNA (siRNA) to maintain HIV permanently in a state of super latency, and CRISPR gRNA to excise the latent reservoir. A challenge with progressing RNA therapeutics to the clinic is achieving effective delivery into the host cell. This review covers recent nanotechnological strategies for siRNA delivery using liposomes, N-acetylgalactosamine conjugation, inorganic nanoparticles and polymer-based nanocapsules. We further discuss the opportunities and challenges of those strategies for HIV treatment.
format Online
Article
Text
id pubmed-9324444
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-93244442022-07-27 Targeted Nanocarrier Delivery of RNA Therapeutics to Control HIV Infection Agbosu, Esinam E. Ledger, Scott Kelleher, Anthony D. Wen, Jing Ahlenstiel, Chantelle L. Pharmaceutics Review Our understanding of HIV infection has greatly advanced since the discovery of the virus in 1983. Treatment options have improved the quality of life of people living with HIV/AIDS, turning it from a fatal disease into a chronic, manageable infection. Despite all this progress, a cure remains elusive. A major barrier to attaining an HIV cure is the presence of the latent viral reservoir, which is established early in infection and persists for the lifetime of the host, even during prolonged anti-viral therapy. Different cure strategies are currently being explored to eliminate or suppress this reservoir. Several studies have shown that a functional cure may be achieved by preventing infection and also inhibiting reactivation of the virus from the latent reservoir. Here, we briefly describe the main HIV cure strategies, focussing on the use of RNA therapeutics, including small interfering RNA (siRNA) to maintain HIV permanently in a state of super latency, and CRISPR gRNA to excise the latent reservoir. A challenge with progressing RNA therapeutics to the clinic is achieving effective delivery into the host cell. This review covers recent nanotechnological strategies for siRNA delivery using liposomes, N-acetylgalactosamine conjugation, inorganic nanoparticles and polymer-based nanocapsules. We further discuss the opportunities and challenges of those strategies for HIV treatment. MDPI 2022-06-26 /pmc/articles/PMC9324444/ /pubmed/35890248 http://dx.doi.org/10.3390/pharmaceutics14071352 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Agbosu, Esinam E.
Ledger, Scott
Kelleher, Anthony D.
Wen, Jing
Ahlenstiel, Chantelle L.
Targeted Nanocarrier Delivery of RNA Therapeutics to Control HIV Infection
title Targeted Nanocarrier Delivery of RNA Therapeutics to Control HIV Infection
title_full Targeted Nanocarrier Delivery of RNA Therapeutics to Control HIV Infection
title_fullStr Targeted Nanocarrier Delivery of RNA Therapeutics to Control HIV Infection
title_full_unstemmed Targeted Nanocarrier Delivery of RNA Therapeutics to Control HIV Infection
title_short Targeted Nanocarrier Delivery of RNA Therapeutics to Control HIV Infection
title_sort targeted nanocarrier delivery of rna therapeutics to control hiv infection
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9324444/
https://www.ncbi.nlm.nih.gov/pubmed/35890248
http://dx.doi.org/10.3390/pharmaceutics14071352
work_keys_str_mv AT agbosuesiname targetednanocarrierdeliveryofrnatherapeuticstocontrolhivinfection
AT ledgerscott targetednanocarrierdeliveryofrnatherapeuticstocontrolhivinfection
AT kelleheranthonyd targetednanocarrierdeliveryofrnatherapeuticstocontrolhivinfection
AT wenjing targetednanocarrierdeliveryofrnatherapeuticstocontrolhivinfection
AT ahlenstielchantellel targetednanocarrierdeliveryofrnatherapeuticstocontrolhivinfection