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Performance characteristics of an antibody-based multiplex kit for determining recent HIV-1 infection
The availability of reliable laboratory methods for determining recent HIV infection is vital for accurate estimation of population-based incidence. The mean duration of recent infection (MDRI) and false recent rate (FRR) are critical parameters for HIV incidence assays, as they impact HIV incidence...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5417525/ https://www.ncbi.nlm.nih.gov/pubmed/28472089 http://dx.doi.org/10.1371/journal.pone.0176593 |
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author | Curtis, Kelly A. Hanson, Debra L. Price, Krystin Ambrose Owen, S. Michele |
author_facet | Curtis, Kelly A. Hanson, Debra L. Price, Krystin Ambrose Owen, S. Michele |
author_sort | Curtis, Kelly A. |
collection | PubMed |
description | The availability of reliable laboratory methods for determining recent HIV infection is vital for accurate estimation of population-based incidence. The mean duration of recent infection (MDRI) and false recent rate (FRR) are critical parameters for HIV incidence assays, as they impact HIV incidence estimates and provide a measure of assay performance. The HIV-1 Multiplex assay is an in-house developed, magnetic bead-based assay that measures virus-specific antibody levels and avidity to multiple analytes. To ensure quality control and to facilitate transfer of the assay to external laboratories or testing facilities, the in-house assay has been adapted and produced in kit form. Here, we describe the performance characteristics of the multiplex kit and demonstrate the stability of the kit components over a one-year period. Two statistical methods were employed to estimate the MDRI of the individual analytes and five different algorithms, combining multiple analyte values. The MDRI estimates for the individual analytes and five algorithms were all between 200 and 300 days post-seroconversion, with no notable difference between the two statistical approaches. All five algorithms exhibited a 0% FRR with specimens from long-term, subtype B HIV-1-infected individuals. The assay parameters described in this study provide the necessary tools to implement the HIV-1 multiplex assay and improves the utility of the assay for field use. |
format | Online Article Text |
id | pubmed-5417525 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-54175252017-05-14 Performance characteristics of an antibody-based multiplex kit for determining recent HIV-1 infection Curtis, Kelly A. Hanson, Debra L. Price, Krystin Ambrose Owen, S. Michele PLoS One Research Article The availability of reliable laboratory methods for determining recent HIV infection is vital for accurate estimation of population-based incidence. The mean duration of recent infection (MDRI) and false recent rate (FRR) are critical parameters for HIV incidence assays, as they impact HIV incidence estimates and provide a measure of assay performance. The HIV-1 Multiplex assay is an in-house developed, magnetic bead-based assay that measures virus-specific antibody levels and avidity to multiple analytes. To ensure quality control and to facilitate transfer of the assay to external laboratories or testing facilities, the in-house assay has been adapted and produced in kit form. Here, we describe the performance characteristics of the multiplex kit and demonstrate the stability of the kit components over a one-year period. Two statistical methods were employed to estimate the MDRI of the individual analytes and five different algorithms, combining multiple analyte values. The MDRI estimates for the individual analytes and five algorithms were all between 200 and 300 days post-seroconversion, with no notable difference between the two statistical approaches. All five algorithms exhibited a 0% FRR with specimens from long-term, subtype B HIV-1-infected individuals. The assay parameters described in this study provide the necessary tools to implement the HIV-1 multiplex assay and improves the utility of the assay for field use. Public Library of Science 2017-05-04 /pmc/articles/PMC5417525/ /pubmed/28472089 http://dx.doi.org/10.1371/journal.pone.0176593 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication. |
spellingShingle | Research Article Curtis, Kelly A. Hanson, Debra L. Price, Krystin Ambrose Owen, S. Michele Performance characteristics of an antibody-based multiplex kit for determining recent HIV-1 infection |
title | Performance characteristics of an antibody-based multiplex kit for determining recent HIV-1 infection |
title_full | Performance characteristics of an antibody-based multiplex kit for determining recent HIV-1 infection |
title_fullStr | Performance characteristics of an antibody-based multiplex kit for determining recent HIV-1 infection |
title_full_unstemmed | Performance characteristics of an antibody-based multiplex kit for determining recent HIV-1 infection |
title_short | Performance characteristics of an antibody-based multiplex kit for determining recent HIV-1 infection |
title_sort | performance characteristics of an antibody-based multiplex kit for determining recent hiv-1 infection |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5417525/ https://www.ncbi.nlm.nih.gov/pubmed/28472089 http://dx.doi.org/10.1371/journal.pone.0176593 |
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