Evidence map›Paper›PMID 39453903›Full record

ArticlePloS one2024

Determination of the mean duration of recent infection and false recency rate for the HIV triplex multiplex bead assay.

Robert A Domaoal, Jeni Vuong, Amy Zheng, Mervi Detorio, Bharat S Parekh, Ernest L Yufenyuy

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Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Robert A DomaoalDivision of Global HIV & TB, Centers for Disease Control and Prevention, Atlanta, GA, United States of America.ORCID 0000-0002-0629-9459
Jeni VuongDivision of Global HIV & TB, Centers for Disease Control and Prevention, Atlanta, GA, United States of America.ORCID 0000-0002-2038-6356
Amy ZhengDivision of Global HIV & TB, Centers for Disease Control and Prevention, Atlanta, GA, United States of America.ORCID 0000-0003-3048-3667
Mervi DetorioDivision of Global HIV & TB, Centers for Disease Control and Prevention, Atlanta, GA, United States of America.
Bharat S ParekhDivision of Global HIV & TB, Centers for Disease Control and Prevention, Atlanta, GA, United States of America.ORCID 0000-0002-1088-4263
Ernest L YufenyuyDivision of Global HIV & TB, Centers for Disease Control and Prevention, Atlanta, GA, United States of America.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWe developed the HIV Triplex multiplex bead assay to identify and serotype HIV infection with high sensitivity and specificity; and distinguish recent from long-term HIV-1 infections. It can facilitate accurate incidence estimation, while reducing the number of tests and blood collected, which is highly desirable for use in future studies and surveys. Using previously collected, treatment-naive longitudinal seroconversion HIV-1 positive panels and specimens from individuals infected for >12 months, we determined the assay's mean duration of recent infection (MDRI) and false-recency rate (FRR) respectively, at various mean fluorescent intensity (MFI) cutoffs.

methodsWe tested seroconversion specimens (N = 814) from 142 individuals infected with HIV-1 subtypes B, C, or AE, and 1341 cross-sectional specimens from individuals infected >12 months. The MFI cutoffs of 1000 to 2000 were evaluated for recency classification, including an MFI of 1250 corresponding to the limiting antigen avidity enzyme immunoassay (LAg-EIA) cutoff of 1.5 normalized optical density for MDRI and FRR. We used four statistical methods: Methods 1 and 2 used the empirically balanced observation time approach. Method 2 MFI values were raised to power = 1.33, based on a repeated measures model to linearize the relationship between MFI and time points, whereas Method 1 was not linearized. Methods 3 and 4 employed quadratic and linear interpolations for each seroconversion panel. FRR was calculated by dividing the number of specimens misclassified as recent by the total number of specimens tested.

resultsMDRI values ranged from 135-146 days at MFI = 1000 to 229-279 days at MFI = 2000 by the 4 methods. FRR varied from 0.15%-1.27% with increasing MFI cutoff. At MFI = 1250, the average MDRI of 4 methods was 169 days and ranged from 159-183 with overlapping 95% CIs and FRR = 0.52%.

conclusionThe HIV Triplex assay demonstrates a longer dynamic range compared to current HIV recency assays with a low FRR for cutoffs examined. With a longer dynamic range and low FRR, the MDRI for recent infection can be extended as appropriate to detect more recent infections, increasing the value of incidence assays benefiting public health surveillance and future surveys.

Indexed as

HIV-1HIV InfectionsCross-Sectional StudiesHIV AntibodiesHumansSensitivity and SpecificitySeroconversionTime FactorsHIV Antibodies

Identifiers

PMID39453903
PMCPMC11508083

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.