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Recalibration of the Limiting Antigen Avidity EIA to Determine Mean Duration of Recent Infection in Divergent HIV-1 Subtypes

Authors :
Alex Welte
Yan Jiang
John N. Nkengasong
Boonyos Raengsakulrach
Anindya K. De
Maofeng Qiu
Neha Shah
Trudy Dobbs
Reshma Kassanjee
Marcel E. Curlin
Meade Morgan
Michael Martin
Bharat Parekh
Suphak Vanichseni
Chonticha Kittinunvorakoon
Linh Vi Le
Haiying Yu
Andrea A. Kim
Yan Hao
William Ampofo
Yen T. Duong
Kachit Choopanya
Erin K. Rottinghaus
Tuan Anh Nguyen
Source :
PLoS ONE, PLoS ONE, Vol 10, Iss 2, p e0114947 (2015)
Publication Year :
2015
Publisher :
Public Library of Science (PLoS), 2015.

Abstract

Background Mean duration of recent infection (MDRI) and misclassification of long-term HIV-1 infections, as proportion false recent (PFR), are critical parameters for laboratory-based assays for estimating HIV-1 incidence. Recent review of the data by us and others indicated that MDRI of LAg-Avidity EIA estimated previously required recalibration. We present here results of recalibration efforts using >250 seroconversion panels and multiple statistical methods to ensure accuracy and consensus. Methods A total of 2737 longitudinal specimens collected from 259 seroconverting individuals infected with diverse HIV-1 subtypes were tested with the LAg-Avidity EIA as previously described. Data were analyzed for determination of MDRI at ODn cutoffs of 1.0 to 2.0 using 7 statistical approaches and sub-analyzed by HIV-1 subtypes. In addition, 3740 specimens from individuals with infection >1 year, including 488 from patients with AIDS, were tested for PFR at varying cutoffs. Results Using different statistical methods, MDRI values ranged from 88–94 days at cutoff ODn = 1.0 to 177–183 days at ODn = 2.0. The MDRI values were similar by different methods suggesting coherence of different approaches. Testing for misclassification among long-term infections indicated that overall PFRs were 0.6% to 2.5% at increasing cutoffs of 1.0 to 2.0, respectively. Balancing the need for a longer MDRI and smaller PFR (

Details

ISSN :
19326203
Volume :
10
Database :
OpenAIRE
Journal :
PLOS ONE
Accession number :
edsair.doi.dedup.....31c86fb8e7baf7949823485778e18f85