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In-house ELISA protocols for capsid p24 detection of diverse HIV isolates

BACKGROUND: The capsid p24 (CA-p24) antigen is a component of the viral capsid of human immunodeficiency virus (HIV) that has been commonly used for clinical diagnosis and monitoring of HIV infections in Enzyme-linked Immunosorbent Assays (ELISAs). Commercial CA-p24 ELISAs are widely used in researc...

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Autores principales: Molina, Mariano A., Vink, Monique, Berkhout, Ben, Herrera-Carrillo, Elena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10656996/
https://www.ncbi.nlm.nih.gov/pubmed/37978551
http://dx.doi.org/10.1186/s12985-023-02242-5
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author Molina, Mariano A.
Vink, Monique
Berkhout, Ben
Herrera-Carrillo, Elena
author_facet Molina, Mariano A.
Vink, Monique
Berkhout, Ben
Herrera-Carrillo, Elena
author_sort Molina, Mariano A.
collection PubMed
description BACKGROUND: The capsid p24 (CA-p24) antigen is a component of the viral capsid of human immunodeficiency virus (HIV) that has been commonly used for clinical diagnosis and monitoring of HIV infections in Enzyme-linked Immunosorbent Assays (ELISAs). Commercial CA-p24 ELISAs are widely used in research settings, but these kits are costly and have limited breadth for detecting diverse HIV isolates. METHODS: Commercial CA-p24 antibodies were used as capture and detection antibodies. Specific CA-p24 ELISAs were established with these antibodies and tested for the detection of HIV-1 isolates with the aim of developing in-house protocols to recognize HIV-1 infections in vitro for research purposes. RESULTS: Here we present four protocols for in-house ELISAs to detect HIV CA-p24 using commercial antibodies. The assays were able to detect the CA-p24 antigen of different HIV-1 isolates tested. Comparison between the protocols showed that these in-house ELISAs exhibit high specificity, sensitivity, and reproducibility for CA-p24 quantitation but their reactivity varied per HIV-1 isolate and subtype. CONCLUSIONS: These optimized ELISA protocols represent valuable tools to investigate HIV-1 infections in research facilities at a lower price than commercial CA-p24 kits. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12985-023-02242-5.
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spelling pubmed-106569962023-11-17 In-house ELISA protocols for capsid p24 detection of diverse HIV isolates Molina, Mariano A. Vink, Monique Berkhout, Ben Herrera-Carrillo, Elena Virol J Methodology BACKGROUND: The capsid p24 (CA-p24) antigen is a component of the viral capsid of human immunodeficiency virus (HIV) that has been commonly used for clinical diagnosis and monitoring of HIV infections in Enzyme-linked Immunosorbent Assays (ELISAs). Commercial CA-p24 ELISAs are widely used in research settings, but these kits are costly and have limited breadth for detecting diverse HIV isolates. METHODS: Commercial CA-p24 antibodies were used as capture and detection antibodies. Specific CA-p24 ELISAs were established with these antibodies and tested for the detection of HIV-1 isolates with the aim of developing in-house protocols to recognize HIV-1 infections in vitro for research purposes. RESULTS: Here we present four protocols for in-house ELISAs to detect HIV CA-p24 using commercial antibodies. The assays were able to detect the CA-p24 antigen of different HIV-1 isolates tested. Comparison between the protocols showed that these in-house ELISAs exhibit high specificity, sensitivity, and reproducibility for CA-p24 quantitation but their reactivity varied per HIV-1 isolate and subtype. CONCLUSIONS: These optimized ELISA protocols represent valuable tools to investigate HIV-1 infections in research facilities at a lower price than commercial CA-p24 kits. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12985-023-02242-5. BioMed Central 2023-11-17 /pmc/articles/PMC10656996/ /pubmed/37978551 http://dx.doi.org/10.1186/s12985-023-02242-5 Text en © The Author(s) 2023 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Methodology
Molina, Mariano A.
Vink, Monique
Berkhout, Ben
Herrera-Carrillo, Elena
In-house ELISA protocols for capsid p24 detection of diverse HIV isolates
title In-house ELISA protocols for capsid p24 detection of diverse HIV isolates
title_full In-house ELISA protocols for capsid p24 detection of diverse HIV isolates
title_fullStr In-house ELISA protocols for capsid p24 detection of diverse HIV isolates
title_full_unstemmed In-house ELISA protocols for capsid p24 detection of diverse HIV isolates
title_short In-house ELISA protocols for capsid p24 detection of diverse HIV isolates
title_sort in-house elisa protocols for capsid p24 detection of diverse hiv isolates
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10656996/
https://www.ncbi.nlm.nih.gov/pubmed/37978551
http://dx.doi.org/10.1186/s12985-023-02242-5
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