Evidence map›Paper›PMID 40202973›Full record

ArticlePLOS global public health2025

Field validation and application of the luminex triplex HIV assay to estimate HIV prevalence and HIV-1 incidence in Nigeria.

Ernest L Yufenyuy, Olusola A Akanbi, Vedapuri Shanmugam, Kelsie Decker-Pulice, Jeni Vuong, Mervi Detorio, Amy Zheng, Orji Bassey, Ado G Abubakar, Oluwaseun Akinmulero and 17 more

Abstract read
In one paragraph

Article in PLOS global public health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

27 authors.

Ernest L YufenyuyDivision of Global HIV & TB, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.ORCID https://orcid.org/0000-0002-0613-1373
Olusola A AkanbiPublic Health Institute/Centers for Disease Control, Global Health Fellowship Program, Atlanta, Georgia, United States of America.
Vedapuri ShanmugamDivision of Global HIV & TB, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.ORCID https://orcid.org/0000-0003-3612-1085
Kelsie Decker-PuliceDivision of Global HIV & TB, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
Jeni VuongDivision of Global HIV & TB, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.ORCID https://orcid.org/0000-0002-2038-6356
Mervi DetorioDivision of Global HIV & TB, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.ORCID https://orcid.org/0009-0000-8114-2112
Amy ZhengDivision of Global HIV & TB, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
Orji BasseyDivision of Global HIV & TB, United States Centers for Disease Control and Prevention, Abuja, Nigeria.
Ado G AbubakarLaboratory Quality Improvement Unit, Institute of Human Virology, Abuja, Nigeria.
Oluwaseun AkinmuleroLaboratory Quality Improvement Unit, Institute of Human Virology, Abuja, Nigeria.
Mudiaga EsiekpeLaboratory Quality Improvement Unit, Institute of Human Virology, Abuja, Nigeria.
Andrew ThomasLaboratory Quality Improvement Unit, Institute of Human Virology, Abuja, Nigeria.
Iliyasu Abubakar BichiLaboratory Quality Improvement Unit, Institute of Human Virology, Abuja, Nigeria.
Israel TamunonengiyeoforiLaboratory Quality Improvement Unit, Institute of Human Virology, Abuja, Nigeria.
Chinwe UgwuLaboratory Quality Improvement Unit, Institute of Human Virology, Abuja, Nigeria.
Evbuomwan ErasogieNigeria Centre for Disease Control and Prevention, Abuja, Nigeria.
William NwachukwuNigeria Centre for Disease Control and Prevention, Abuja, Nigeria.ORCID https://orcid.org/0000-0001-7111-1320
Nwando MbaNigeria Centre for Disease Control and Prevention, Abuja, Nigeria.
Ndidi AgalaLaboratory Quality Improvement Unit, Institute of Human Virology, Abuja, Nigeria.
Megan BronsonDivision of Global HIV & TB, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
Hetal K PatelDivision of Global HIV & TB, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.ORCID https://orcid.org/0000-0002-5468-2591
Nnaemeka C IriemenemDivision of Global HIV & TB, United States Centers for Disease Control and Prevention, Abuja, Nigeria.ORCID https://orcid.org/0000-0003-2187-8894
Stacie GrebyDivision of Global HIV & TB, United States Centers for Disease Control and Prevention, Abuja, Nigeria.
McPaul I OkoyeDivision of Global HIV & TB, United States Centers for Disease Control and Prevention, Abuja, Nigeria.
Mahesh SwaminathanDivision of Global HIV & TB, United States Centers for Disease Control and Prevention, Abuja, Nigeria.ORCID https://orcid.org/0000-0001-5827-3245
Bharat S ParekhDivision of Global HIV & TB, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.ORCID https://orcid.org/0000-0002-1088-4263
Chikwe IhekweazuNigeria Centre for Disease Control and Prevention, Abuja, Nigeria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

HIV cross-sectional surveys require multi-layered testing with several tests to estimate HIV prevalence and HIV-1 incidence. We evaluated the performance and accuracy of the newly developed HIV Triplex assay to diagnose HIV-1 and HIV-2 and detect HIV-1 recent infections using plasma samples from the 2018 Nigeria AIDS Indicator and Impact Survey (NAIIS). Plasma samples from consenting HIV-positive (n=2,773) and a subset of HIV-negative samples (n=7,196), as determined by the national rapid testing algorithm, followed by Bio-Rad Geenius HIV-1/2 Supplemental Assay and Western Blot, aged 18 months - 64 years, were tested using the Luminex-based HIV Triplex assay. The assay classified specimens as HIV-1 positive, HIV-2 positive, dual (HIV-1 & 2) infections, or HIV-seronegative. All HIV-1 and dual infections were further classified as either HIV-1 recent (<6 months) or long-term (LT) based on mean fluorescent intensities and compared with the LAg-Avidity EIA as the reference. Multiplex results were analyzed and compared with the final NAIIS survey data for unweighted HIV prevalence and HIV-1 incidence. The diagnostic sensitivity and specificity of the HIV Triplex assay was 99.71% and 99.37%, respectively, with a kappa of 0.987 when compared to NAIIS survey results. Percent agreement between the HIV Triplex assay and the LAg-Avidity EIA for recent and LT classification was 98.86% with a kappa of 0.80 [CI: 0.71-0.89] and a Spearman-ranked correlation (ρ) of 0.689. A small number (n=45; 0.63%) of the subset of negatives tested were classified by the multiplex assay as either HIV-1 positive (n=35) or HIV-2 positive (n=10). Nevertheless, the HIV Triplex assay agreed with NAIIS HIV-negative survey results (99.37%). Using these results as they were, unweighted estimates of HIV prevalence for both HIV Triplex assay and NAIIS test results were similar (1.62% [95% CI: 1.56-1.68] and 1.60% [95% CI: 1.54-1.66], respectively) with overlapping confidence. After adjusting for viral load and anti-retroviral therapy, HIV-1 unweighted incidence for ages ≥15 years, using HIV Triplex assay data, was 0.70 per 1,000 [95% CI: 0.40-0.90]. This is similar to the unweighted incidence using the LAg-based RITA (recent infection testing algorithm) of 0.80 per 1,000 [95% CI: 0.60-1.10]. The HIV Triplex assay combines several assays in one, providing highly accurate results for estimating HIV prevalence and HIV-1 incidence in surveys. This assay has the potential to simplify cross-sectional surveys making them less expensive, easier, and quicker.

Identifiers

PMID40202973
PMCPMC11981228

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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.