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Difficulties of Identifying the Early HIV Antibody Seroconversion Period Depending on the Confirmatory Assay

BACKGROUND: Identification of HIV infection at the early stage is valuable for patient management, for prevention, and for research purposes. In practice, identification of a recent HIV infection at diagnosis proves challenging after HIV antibody seroconversion but can be suspected using Western blo...

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Autores principales: Stefic, Karl, Mahjoub, Nadia, Desouche, Céline, Néré, Marie Laure, Thierry, Damien, Delaugerre, Constance, Barin, Francis, Chaix, Marie Laure
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7246347/
https://www.ncbi.nlm.nih.gov/pubmed/32478120
http://dx.doi.org/10.1093/ofid/ofaa140
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author Stefic, Karl
Mahjoub, Nadia
Desouche, Céline
Néré, Marie Laure
Thierry, Damien
Delaugerre, Constance
Barin, Francis
Chaix, Marie Laure
author_facet Stefic, Karl
Mahjoub, Nadia
Desouche, Céline
Néré, Marie Laure
Thierry, Damien
Delaugerre, Constance
Barin, Francis
Chaix, Marie Laure
author_sort Stefic, Karl
collection PubMed
description BACKGROUND: Identification of HIV infection at the early stage is valuable for patient management, for prevention, and for research purposes. In practice, identification of a recent HIV infection at diagnosis proves challenging after HIV antibody seroconversion but can be suspected using Western blots (WBs) or immunoblots (IBs) as confirmatory assays. METHODS: Five commercially available confirmatory assays were compared using 43 samples from recently infected individuals. This included 2 WBs (New LAV Blot I, Biorad, and HIV Blot 2.2, MP Biomedicals), 2 IBs (INNO-LIA HIV I/II, Fujirebio, and RecomLine HIV-1 & HIV-2, Mikrogen Diagnostik), and 1 immunochromatographic single-use assay (Geenius HIV1/2 supplemental assay, Biorad). RESULTS: Following the manufacturer’s recommendations for interpretation, the 2 WBs led to indeterminate results for 30% and 42% of the samples, suggesting recent infection, compared with 2%–7% for the 3 other assays. When interpreted based on the Fiebig classification, concordant stages were observed in 42% of samples, and only 49% were classified as early seroconversion by all 5 assays. For the remaining specimens, the distinction with chronic infection was highly variable depending on the assay (5%–100%). CONCLUSIONS: Clinical laboratories must consider this variability, which must be kept in mind both for initial diagnosis and for multicenter studies for which inclusion criteria refer to serological profiles by confirmatory assays.
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spelling pubmed-72463472020-05-28 Difficulties of Identifying the Early HIV Antibody Seroconversion Period Depending on the Confirmatory Assay Stefic, Karl Mahjoub, Nadia Desouche, Céline Néré, Marie Laure Thierry, Damien Delaugerre, Constance Barin, Francis Chaix, Marie Laure Open Forum Infect Dis Major Article BACKGROUND: Identification of HIV infection at the early stage is valuable for patient management, for prevention, and for research purposes. In practice, identification of a recent HIV infection at diagnosis proves challenging after HIV antibody seroconversion but can be suspected using Western blots (WBs) or immunoblots (IBs) as confirmatory assays. METHODS: Five commercially available confirmatory assays were compared using 43 samples from recently infected individuals. This included 2 WBs (New LAV Blot I, Biorad, and HIV Blot 2.2, MP Biomedicals), 2 IBs (INNO-LIA HIV I/II, Fujirebio, and RecomLine HIV-1 & HIV-2, Mikrogen Diagnostik), and 1 immunochromatographic single-use assay (Geenius HIV1/2 supplemental assay, Biorad). RESULTS: Following the manufacturer’s recommendations for interpretation, the 2 WBs led to indeterminate results for 30% and 42% of the samples, suggesting recent infection, compared with 2%–7% for the 3 other assays. When interpreted based on the Fiebig classification, concordant stages were observed in 42% of samples, and only 49% were classified as early seroconversion by all 5 assays. For the remaining specimens, the distinction with chronic infection was highly variable depending on the assay (5%–100%). CONCLUSIONS: Clinical laboratories must consider this variability, which must be kept in mind both for initial diagnosis and for multicenter studies for which inclusion criteria refer to serological profiles by confirmatory assays. Oxford University Press 2020-04-21 /pmc/articles/PMC7246347/ /pubmed/32478120 http://dx.doi.org/10.1093/ofid/ofaa140 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Major Article
Stefic, Karl
Mahjoub, Nadia
Desouche, Céline
Néré, Marie Laure
Thierry, Damien
Delaugerre, Constance
Barin, Francis
Chaix, Marie Laure
Difficulties of Identifying the Early HIV Antibody Seroconversion Period Depending on the Confirmatory Assay
title Difficulties of Identifying the Early HIV Antibody Seroconversion Period Depending on the Confirmatory Assay
title_full Difficulties of Identifying the Early HIV Antibody Seroconversion Period Depending on the Confirmatory Assay
title_fullStr Difficulties of Identifying the Early HIV Antibody Seroconversion Period Depending on the Confirmatory Assay
title_full_unstemmed Difficulties of Identifying the Early HIV Antibody Seroconversion Period Depending on the Confirmatory Assay
title_short Difficulties of Identifying the Early HIV Antibody Seroconversion Period Depending on the Confirmatory Assay
title_sort difficulties of identifying the early hiv antibody seroconversion period depending on the confirmatory assay
topic Major Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7246347/
https://www.ncbi.nlm.nih.gov/pubmed/32478120
http://dx.doi.org/10.1093/ofid/ofaa140
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