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Outlook for CRISPR-based tuberculosis assays now in their infancy

Tuberculosis (TB) remains a major underdiagnosed public health threat worldwide, being responsible for more than 10 million cases and one million deaths annually. TB diagnosis has become more rapid with the development and adoption of molecular tests, but remains challenging with traditional TB diag...

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Autores principales: Huang, Zhen, Zhang, Guoliang, Lyon, Christopher J., Hu, Tony Y., Lu, Shuihua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10436990/
https://www.ncbi.nlm.nih.gov/pubmed/37600797
http://dx.doi.org/10.3389/fimmu.2023.1172035
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author Huang, Zhen
Zhang, Guoliang
Lyon, Christopher J.
Hu, Tony Y.
Lu, Shuihua
author_facet Huang, Zhen
Zhang, Guoliang
Lyon, Christopher J.
Hu, Tony Y.
Lu, Shuihua
author_sort Huang, Zhen
collection PubMed
description Tuberculosis (TB) remains a major underdiagnosed public health threat worldwide, being responsible for more than 10 million cases and one million deaths annually. TB diagnosis has become more rapid with the development and adoption of molecular tests, but remains challenging with traditional TB diagnosis, but there has not been a critical review of this area. Here, we systematically review these approaches to assess their diagnostic potential and issues with the development and clinical evaluation of proposed CRISPR-based TB assays. Based on these observations, we propose constructive suggestions to improve sample pretreatment, method development, clinical validation, and accessibility of these assays to streamline future assay development and validation studies.
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spelling pubmed-104369902023-08-19 Outlook for CRISPR-based tuberculosis assays now in their infancy Huang, Zhen Zhang, Guoliang Lyon, Christopher J. Hu, Tony Y. Lu, Shuihua Front Immunol Immunology Tuberculosis (TB) remains a major underdiagnosed public health threat worldwide, being responsible for more than 10 million cases and one million deaths annually. TB diagnosis has become more rapid with the development and adoption of molecular tests, but remains challenging with traditional TB diagnosis, but there has not been a critical review of this area. Here, we systematically review these approaches to assess their diagnostic potential and issues with the development and clinical evaluation of proposed CRISPR-based TB assays. Based on these observations, we propose constructive suggestions to improve sample pretreatment, method development, clinical validation, and accessibility of these assays to streamline future assay development and validation studies. Frontiers Media S.A. 2023-08-03 /pmc/articles/PMC10436990/ /pubmed/37600797 http://dx.doi.org/10.3389/fimmu.2023.1172035 Text en Copyright © 2023 Huang, Zhang, Lyon, Hu and Lu https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Huang, Zhen
Zhang, Guoliang
Lyon, Christopher J.
Hu, Tony Y.
Lu, Shuihua
Outlook for CRISPR-based tuberculosis assays now in their infancy
title Outlook for CRISPR-based tuberculosis assays now in their infancy
title_full Outlook for CRISPR-based tuberculosis assays now in their infancy
title_fullStr Outlook for CRISPR-based tuberculosis assays now in their infancy
title_full_unstemmed Outlook for CRISPR-based tuberculosis assays now in their infancy
title_short Outlook for CRISPR-based tuberculosis assays now in their infancy
title_sort outlook for crispr-based tuberculosis assays now in their infancy
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10436990/
https://www.ncbi.nlm.nih.gov/pubmed/37600797
http://dx.doi.org/10.3389/fimmu.2023.1172035
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