Hargrove John W, van Schalkwyk Cari, Humphrey Jean H, Mutasa Kuda, Ntozini Robert, Owen Sherry Michele, Masciotra Silvina, Parekh Bharat S, Duong Yen T, Dobbs Trudy, Kilmarx Peter H, Gonese Elizabeth
1 The South African DST/NRF Centre of Excellence in Epidemiological Modelling and Analysis (SACEMA), University of Stellenbosch , Stellenbosch, South Africa .
2 Zvitambo Institute for Maternal and Child Health Research , Harare, Zimbabwe .
AIDS Res Hum Retroviruses. 2017 Sep;33(9):902-904. doi: 10.1089/AID.2016.0319. Epub 2017 May 24.
Laboratory assays that identify recent HIV infections are important for assessing impacts of interventions aimed at reducing HIV incidence. Kinetics of HIV humoral responses can vary with inherent assay properties, and between HIV subtypes, populations, and physiological states. They are important in determining mean duration of recent infection (MDRI) for antibody-based assays for detecting recent HIV infections. We determined MDRIs for multi-subtype peptide representing subtypes B, E and D (BED)-capture enzyme immunoassay, limiting antigen (LAg), and Bio-Rad Avidity Incidence (BRAI) assays for 101 seroconverting postpartum women, recruited in Harare from 1997 to 2000 during the Zimbabwe Vitamin A for Mothers and Babies trial, comparing them against published MDRIs estimated from seroconverting cases in the general population. We also compared MDRIs for women who seroconverted either during the first 9 months, or at later stages, postpartum. At cutoffs (C) of 0.8 for BED, 1.5 for LAg, and 40% for BRAI, estimated MDRIs for postpartum mothers were 192, 104, and 144 days, 33%, 32%, and 52% lower than published estimates of 287, 152 and 298 days, respectively, for clade C samples from general populations. Point estimates of MDRI values were 7%-19% shorter for women who seroconverted in the first 9 months postpartum than for those seroconverting later. MDRI values for three HIV incidence biomarkers are longer in the general population than among postpartum women, particularly those who recently gave birth, consistent with heightened immunological activation soon after birth. Our results provide a caution that MDRI may vary significantly between subjects in different physiological states.
识别近期HIV感染的实验室检测对于评估旨在降低HIV发病率的干预措施的影响至关重要。HIV体液反应的动力学可能因检测方法的固有特性以及HIV亚型、人群和生理状态的不同而有所差异。它们对于基于抗体的检测近期HIV感染的方法确定近期感染的平均持续时间(MDRI)很重要。我们确定了1997年至2000年在津巴布韦母婴维生素A试验期间于哈拉雷招募的101名产后血清转换女性的多亚型肽(代表B、E和D亚型)捕获酶免疫测定、限量抗原(LAg)和伯乐亲和力发病率(BRAI)检测的MDRI,并将其与根据普通人群血清转换病例估计的已发表MDRI进行比较。我们还比较了产后前9个月内或后期血清转换的女性的MDRI。在BED检测的临界值(C)为0.8、LAg检测的临界值为1.5、BRAI检测的临界值为40%时,产后母亲的估计MDRI分别为192天、104天和144天,分别比普通人群C亚型样本的已发表估计值287天、152天和298天低33%、32%和52%。产后前9个月内血清转换的女性的MDRI值的点估计比后期血清转换的女性短7%-19%。普通人群中三种HIV发病率生物标志物的MDRI值比产后女性长,尤其是那些近期分娩的女性,这与出生后不久免疫激活增强一致。我们的结果提醒人们,不同生理状态的受试者之间MDRI可能存在显著差异。