» Articles » PMID: 28318310

Short Communication: Comparison of Maxim and Sedia Limiting Antigen Assay Performance for Measuring HIV Incidence

Overview
Publisher Mary Ann Liebert
Date 2017 Mar 21
PMID 28318310
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

Accurate methods for cross-sectional incidence estimation are needed for HIV prevention research. The Limiting Antigen Avidity (LAg-Avidity) assay has been marketed by two vendors, Maxim Biomedical and Sedia BioSciences Corporation. Performance differences between the two versions of the assay are unknown. We tested a total 1,410 treatment-naive samples with both versions of the assay. The samples came from 176 seroconverters from the Zimbabwe Hormonal Contraception and HIV Study. The correlation between the two versions of the assay was 0.93 for the optical density (OD) and 0.86 for the normalized OD. As the difference was more pronounced for the normalized OD, the difference in assays can be attributed to the calibrators. The mean duration of recent infection (MDRI), the average time individuals infected <2 years appear recently infected, was determined for both versions using an assay cutoff of 1.5 OD-n alone or in combination with a viral load cutoff of >1,000 copies/ml. The MDRI was 137 days for Sedia and 157 days for Maxim, with a difference of 20 days (95% CI 11-30). The MDRIs decreased to 102 and 120 days with the inclusion of a viral load cutoff of >1,000 copies/ml. These results imply that use of the Sedia LAg-Avidity will result in estimates of incidence ∼13% lower than those using the Maxim LAg-Avidity.

Citing Articles

A systematic review of limiting antigen avidity enzyme immunoassay for detection of recent HIV-1 infection to expand supported applications.

Lau J, Murdock N, Murray J, Justman J, Parkin N, Miller V J Virus Erad. 2022; 8(3):100085.

PMID: 36124229 PMC: 9482108. DOI: 10.1016/j.jve.2022.100085.


Use of HIV Recency Assays for HIV Incidence Estimation and Other Surveillance Use Cases: Systematic Review.

Facente S, Grebe E, Maher A, Fox D, Scheer S, Mahy M JMIR Public Health Surveill. 2022; 8(3):e34410.

PMID: 35275085 PMC: 8956992. DOI: 10.2196/34410.


Development of an international external quality assurance program for HIV-1 incidence using the Limiting Antigen Avidity assay.

Keating S, Rountree W, Grebe E, Pappas A, Stone M, Hampton D PLoS One. 2019; 14(9):e0222290.

PMID: 31525218 PMC: 6746377. DOI: 10.1371/journal.pone.0222290.


Performance comparison of the Maxim and Sedia Limiting Antigen Avidity assays for HIV incidence surveillance.

Sempa J, Welte A, Busch M, Hall J, Hampton D, Facente S PLoS One. 2019; 14(7):e0220345.

PMID: 31348809 PMC: 6660077. DOI: 10.1371/journal.pone.0220345.

References
1.
Duong Y, Qiu M, DE A, Jackson K, Dobbs T, Kim A . Detection of recent HIV-1 infection using a new limiting-antigen avidity assay: potential for HIV-1 incidence estimates and avidity maturation studies. PLoS One. 2012; 7(3):e33328. PMC: 3314002. DOI: 10.1371/journal.pone.0033328. View

2.
Morrison C, Richardson B, Mmiro F, Chipato T, Celentano D, Luoto J . Hormonal contraception and the risk of HIV acquisition. AIDS. 2006; 21(1):85-95. DOI: 10.1097/QAD.0b013e3280117c8b. View

3.
Moyo S, Vandormael A, Wilkinson E, Engelbrecht S, Gaseitsiwe S, Kotokwe K . Analysis of Viral Diversity in Relation to the Recency of HIV-1C Infection in Botswana. PLoS One. 2016; 11(8):e0160649. PMC: 4994946. DOI: 10.1371/journal.pone.0160649. View

4.
Duong Y, Kassanjee R, Welte A, Morgan M, De A, Dobbs T . Recalibration of the limiting antigen avidity EIA to determine mean duration of recent infection in divergent HIV-1 subtypes. PLoS One. 2015; 10(2):e0114947. PMC: 4339840. DOI: 10.1371/journal.pone.0114947. View

5.
Kassanjee R, McWalter T, Barnighausen T, Welte A . A new general biomarker-based incidence estimator. Epidemiology. 2012; 23(5):721-8. PMC: 3500970. DOI: 10.1097/EDE.0b013e3182576c07. View