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

HIV HIV antibodies Western blotting recent HIV infection seroconversion

Journal

Open forum infectious diseases
ISSN: 2328-8957
Titre abrégé: Open Forum Infect Dis
Pays: United States
ID NLM: 101637045

Informations de publication

Date de publication:
May 2020
Historique:
received: 23 03 2020
accepted: 17 04 2020
entrez: 2 6 2020
pubmed: 2 6 2020
medline: 2 6 2020
Statut: epublish

Résumé

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. 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). 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%). 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.

Sections du résumé

BACKGROUND 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 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 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 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.

Identifiants

pubmed: 32478120
doi: 10.1093/ofid/ofaa140
pii: ofaa140
pmc: PMC7246347
doi:

Types de publication

Journal Article

Langues

eng

Pagination

ofaa140

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press on behalf of Infectious Diseases Society of America.

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Auteurs

Karl Stefic (K)

Laboratoire de Virologie, CHU Bretonneau, Tours, France.
INSERM U1259, Université de Tours, Tours, France.
Centre National de Référence du Virus de l'Immunodéficience Humaine (VIH), France.

Nadia Mahjoub (N)

Laboratoire de Virologie, CHU Saint Louis, Paris, France.

Céline Desouche (C)

Laboratoire de Virologie, CHU Bretonneau, Tours, France.
Centre National de Référence du Virus de l'Immunodéficience Humaine (VIH), France.

Marie Laure Néré (ML)

Laboratoire de Virologie, CHU Saint Louis, Paris, France.

Damien Thierry (D)

Laboratoire de Virologie, CHU Bretonneau, Tours, France.
Centre National de Référence du Virus de l'Immunodéficience Humaine (VIH), France.

Constance Delaugerre (C)

Laboratoire de Virologie, CHU Saint Louis, Paris, France.
INSERM U944, Université de Paris, Paris, France.
Centre National de Référence du Virus de l'Immunodéficience Humaine (VIH), France.

Francis Barin (F)

Laboratoire de Virologie, CHU Bretonneau, Tours, France.
INSERM U1259, Université de Tours, Tours, France.
Centre National de Référence du Virus de l'Immunodéficience Humaine (VIH), France.

Marie Laure Chaix (ML)

Laboratoire de Virologie, CHU Saint Louis, Paris, France.
INSERM U944, Université de Paris, Paris, France.
Centre National de Référence du Virus de l'Immunodéficience Humaine (VIH), France.

Classifications MeSH