| Literature DB >> 26053661 |
Sallie R Permar, Youyi Fong, Nathan Vandergrift, Genevieve G Fouda, Peter Gilbert, Robert Parks, Frederick H Jaeger, Justin Pollara, Amanda Martelli, Brooke E Liebl, Krissey Lloyd, Nicole L Yates, R Glenn Overman, Xiaoying Shen, Kaylan Whitaker, Haiyan Chen, Jamie Pritchett, Erika Solomon, Emma Friberg, Dawn J Marshall, John F Whitesides, Thaddeus C Gurley, Tarra Von Holle, David R Martinez, Fangping Cai, Amit Kumar, Shi-Mao Xia, Xiaozhi Lu, Raul Louzao, Samantha Wilkes, Saheli Datta, Marcella Sarzotti-Kelsoe, Hua-Xin Liao, Guido Ferrari, S Munir Alam, David C Montefiori, Thomas N Denny, M Anthony Moody, Georgia D Tomaras, Feng Gao, Barton F Haynes.
Abstract
Despite the wide availability of antiretroviral drugs, more than 250,000 infants are vertically infected with HIV-1 annually, emphasizing the need for additional interventions to eliminate pediatric HIV-1 infections. Here, we aimed to define humoral immune correlates of risk of mother-to-child transmission (MTCT) of HIV-1, including responses associated with protection in the RV144 vaccine trial. Eighty-three untreated, HIV-1-transmitting mothers and 165 propensity score-matched nontransmitting mothers were selected from the Women and Infants Transmission Study (WITS) of US nonbreastfeeding, HIV-1-infected mothers. In a multivariable logistic regression model, the magnitude of the maternal IgG responses specific for the third variable loop (V3) of the HIV-1 envelope was predictive of a reduced risk of MTCT. Neutralizing Ab responses against easy-to-neutralize (tier 1) HIV-1 strains also predicted a reduced risk of peripartum transmission in secondary analyses. Moreover, recombinant maternal V3-specific IgG mAbs mediated neutralization of autologous HIV-1 isolates. Thus, common V3-specific Ab responses in maternal plasma predicted a reduced risk of MTCT and mediated autologous virus neutralization, suggesting that boosting these maternal Ab responses may further reduce HIV-1 MTCT.Entities:
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Year: 2015 PMID: 26053661 PMCID: PMC4613557 DOI: 10.1172/JCI81593
Source DB: PubMed Journal: J Clin Invest ISSN: 0021-9738 Impact factor: 14.808