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A click chemistry amplified nanopore assay for ultrasensitive quantification of HIV-1 p24 antigen in clinical samples

Despite major advances in HIV testing, ultrasensitive detection of early infection remains challenging, especially for the viral capsid protein p24, which is an early virological biomarker of HIV-1 infection. Here, To improve p24 detection in patients missed by immunological tests that dominate the...

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Autores principales: Wei, Xiaojun, Wang, Xiaoqin, Zhang, Zehui, Luo, Yuanyuan, Wang, Zixin, Xiong, Wen, Jain, Piyush K., Monnier, John R., Wang, Hui, Hu, Tony Y., Tang, Chuanbing, Albrecht, Helmut, Liu, Chang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9651128/
https://www.ncbi.nlm.nih.gov/pubmed/36369146
http://dx.doi.org/10.1038/s41467-022-34273-x
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author Wei, Xiaojun
Wang, Xiaoqin
Zhang, Zehui
Luo, Yuanyuan
Wang, Zixin
Xiong, Wen
Jain, Piyush K.
Monnier, John R.
Wang, Hui
Hu, Tony Y.
Tang, Chuanbing
Albrecht, Helmut
Liu, Chang
author_facet Wei, Xiaojun
Wang, Xiaoqin
Zhang, Zehui
Luo, Yuanyuan
Wang, Zixin
Xiong, Wen
Jain, Piyush K.
Monnier, John R.
Wang, Hui
Hu, Tony Y.
Tang, Chuanbing
Albrecht, Helmut
Liu, Chang
author_sort Wei, Xiaojun
collection PubMed
description Despite major advances in HIV testing, ultrasensitive detection of early infection remains challenging, especially for the viral capsid protein p24, which is an early virological biomarker of HIV-1 infection. Here, To improve p24 detection in patients missed by immunological tests that dominate the diagnostics market, we show a click chemistry amplified nanopore (CAN) assay for ultrasensitive quantitative detection. This strategy achieves a 20.8 fM (0.5 pg/ml) limit of detection for HIV-1 p24 antigen in human serum, demonstrating 20~100-fold higher analytical sensitivity than nanocluster-based immunoassays and clinically used enzyme-linked immunosorbent assay, respectively. Clinical validation of the CAN assay in a pilot cohort shows p24 quantification at ultra-low concentration range and correlation with CD4 count and viral load. We believe that this strategy can improve the utility of p24 antigen in detecting early infection and monitoring HIV progression and treatment efficacy, and also can be readily modified to detect other infectious diseases.
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spelling pubmed-96511282022-11-14 A click chemistry amplified nanopore assay for ultrasensitive quantification of HIV-1 p24 antigen in clinical samples Wei, Xiaojun Wang, Xiaoqin Zhang, Zehui Luo, Yuanyuan Wang, Zixin Xiong, Wen Jain, Piyush K. Monnier, John R. Wang, Hui Hu, Tony Y. Tang, Chuanbing Albrecht, Helmut Liu, Chang Nat Commun Article Despite major advances in HIV testing, ultrasensitive detection of early infection remains challenging, especially for the viral capsid protein p24, which is an early virological biomarker of HIV-1 infection. Here, To improve p24 detection in patients missed by immunological tests that dominate the diagnostics market, we show a click chemistry amplified nanopore (CAN) assay for ultrasensitive quantitative detection. This strategy achieves a 20.8 fM (0.5 pg/ml) limit of detection for HIV-1 p24 antigen in human serum, demonstrating 20~100-fold higher analytical sensitivity than nanocluster-based immunoassays and clinically used enzyme-linked immunosorbent assay, respectively. Clinical validation of the CAN assay in a pilot cohort shows p24 quantification at ultra-low concentration range and correlation with CD4 count and viral load. We believe that this strategy can improve the utility of p24 antigen in detecting early infection and monitoring HIV progression and treatment efficacy, and also can be readily modified to detect other infectious diseases. Nature Publishing Group UK 2022-11-11 /pmc/articles/PMC9651128/ /pubmed/36369146 http://dx.doi.org/10.1038/s41467-022-34273-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Wei, Xiaojun
Wang, Xiaoqin
Zhang, Zehui
Luo, Yuanyuan
Wang, Zixin
Xiong, Wen
Jain, Piyush K.
Monnier, John R.
Wang, Hui
Hu, Tony Y.
Tang, Chuanbing
Albrecht, Helmut
Liu, Chang
A click chemistry amplified nanopore assay for ultrasensitive quantification of HIV-1 p24 antigen in clinical samples
title A click chemistry amplified nanopore assay for ultrasensitive quantification of HIV-1 p24 antigen in clinical samples
title_full A click chemistry amplified nanopore assay for ultrasensitive quantification of HIV-1 p24 antigen in clinical samples
title_fullStr A click chemistry amplified nanopore assay for ultrasensitive quantification of HIV-1 p24 antigen in clinical samples
title_full_unstemmed A click chemistry amplified nanopore assay for ultrasensitive quantification of HIV-1 p24 antigen in clinical samples
title_short A click chemistry amplified nanopore assay for ultrasensitive quantification of HIV-1 p24 antigen in clinical samples
title_sort click chemistry amplified nanopore assay for ultrasensitive quantification of hiv-1 p24 antigen in clinical samples
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9651128/
https://www.ncbi.nlm.nih.gov/pubmed/36369146
http://dx.doi.org/10.1038/s41467-022-34273-x
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