Maternal HIV-1 envelope-specific antibody responses and reduced risk of perinatal transmission.

نویسندگان

  • 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
چکیده

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.

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عنوان ژورنال:
  • The Journal of clinical investigation

دوره 125 7  شماره 

صفحات  -

تاریخ انتشار 2015