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Antisense Therapy for Infectious Diseases
Infectious diseases, particularly Tuberculosis (TB) caused by Mycobacterium tuberculosis, pose a significant global health challenge, with 1.6 million reported deaths in 2021, making it the most fatal disease caused by a single infectious agent. The rise of drug-resistant infectious diseases adds to...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10453568/ https://www.ncbi.nlm.nih.gov/pubmed/37626929 http://dx.doi.org/10.3390/cells12162119 |
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author | Buthelezi, Lwanda Abonga Pillay, Shandre Ntuli, Noxolo Nokukhanya Gcanga, Lorna Guler, Reto |
author_facet | Buthelezi, Lwanda Abonga Pillay, Shandre Ntuli, Noxolo Nokukhanya Gcanga, Lorna Guler, Reto |
author_sort | Buthelezi, Lwanda Abonga |
collection | PubMed |
description | Infectious diseases, particularly Tuberculosis (TB) caused by Mycobacterium tuberculosis, pose a significant global health challenge, with 1.6 million reported deaths in 2021, making it the most fatal disease caused by a single infectious agent. The rise of drug-resistant infectious diseases adds to the urgency of finding effective and safe intervention therapies. Antisense therapy uses antisense oligonucleotides (ASOs) that are short, chemically modified, single-stranded deoxyribonucleotide molecules complementary to their mRNA target. Due to their designed target specificity and inhibition of a disease-causing gene at the mRNA level, antisense therapy has gained interest as a potential therapeutic approach. This type of therapy is currently utilized in numerous diseases, such as cancer and genetic disorders. Currently, there are limited but steadily increasing studies available that report on the use of ASOs as treatment for infectious diseases. This review explores the sustainability of FDA-approved and preclinically tested ASOs as a treatment for infectious diseases and the adaptability of ASOs for chemical modifications resulting in reduced side effects with improved drug delivery; thus, highlighting the potential therapeutic uses of ASOs for treating infectious diseases. |
format | Online Article Text |
id | pubmed-10453568 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-104535682023-08-26 Antisense Therapy for Infectious Diseases Buthelezi, Lwanda Abonga Pillay, Shandre Ntuli, Noxolo Nokukhanya Gcanga, Lorna Guler, Reto Cells Review Infectious diseases, particularly Tuberculosis (TB) caused by Mycobacterium tuberculosis, pose a significant global health challenge, with 1.6 million reported deaths in 2021, making it the most fatal disease caused by a single infectious agent. The rise of drug-resistant infectious diseases adds to the urgency of finding effective and safe intervention therapies. Antisense therapy uses antisense oligonucleotides (ASOs) that are short, chemically modified, single-stranded deoxyribonucleotide molecules complementary to their mRNA target. Due to their designed target specificity and inhibition of a disease-causing gene at the mRNA level, antisense therapy has gained interest as a potential therapeutic approach. This type of therapy is currently utilized in numerous diseases, such as cancer and genetic disorders. Currently, there are limited but steadily increasing studies available that report on the use of ASOs as treatment for infectious diseases. This review explores the sustainability of FDA-approved and preclinically tested ASOs as a treatment for infectious diseases and the adaptability of ASOs for chemical modifications resulting in reduced side effects with improved drug delivery; thus, highlighting the potential therapeutic uses of ASOs for treating infectious diseases. MDPI 2023-08-21 /pmc/articles/PMC10453568/ /pubmed/37626929 http://dx.doi.org/10.3390/cells12162119 Text en © 2023 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 Buthelezi, Lwanda Abonga Pillay, Shandre Ntuli, Noxolo Nokukhanya Gcanga, Lorna Guler, Reto Antisense Therapy for Infectious Diseases |
title | Antisense Therapy for Infectious Diseases |
title_full | Antisense Therapy for Infectious Diseases |
title_fullStr | Antisense Therapy for Infectious Diseases |
title_full_unstemmed | Antisense Therapy for Infectious Diseases |
title_short | Antisense Therapy for Infectious Diseases |
title_sort | antisense therapy for infectious diseases |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10453568/ https://www.ncbi.nlm.nih.gov/pubmed/37626929 http://dx.doi.org/10.3390/cells12162119 |
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