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Association of HIV-1 Envelope-Specific Breast Milk IgA Responses with Reduced Risk of Postnatal Mother-to-Child Transmission of HIV-1.
Pollara, Justin; McGuire, Erin; Fouda, Genevieve G; Rountree, Wes; Eudailey, Josh; Overman, R Glenn; Seaton, Kelly E; Deal, Aaron; Edwards, R Whitney; Tegha, Gerald; Kamwendo, Deborah; Kumwenda, Jacob; Nelson, Julie A E; Liao, Hua-Xin; Brinkley, Christie; Denny, Thomas N; Ochsenbauer, Christina; Ellington, Sascha; King, Caroline C; Jamieson, Denise J; van der Horst, Charles; Kourtis, Athena P; Tomaras, Georgia D; Ferrari, Guido; Permar, Sallie R.
Afiliação
  • Pollara J; Department of Surgery, Duke University School of Medicine, Durham, North Carolina, USA.
  • McGuire E; Human Vaccine Institute, Duke University School of Medicine, Durham, North Carolina, USA.
  • Fouda GG; Human Vaccine Institute, Duke University School of Medicine, Durham, North Carolina, USA.
  • Rountree W; Human Vaccine Institute, Duke University School of Medicine, Durham, North Carolina, USA.
  • Eudailey J; Human Vaccine Institute, Duke University School of Medicine, Durham, North Carolina, USA.
  • Overman RG; Human Vaccine Institute, Duke University School of Medicine, Durham, North Carolina, USA.
  • Seaton KE; Human Vaccine Institute, Duke University School of Medicine, Durham, North Carolina, USA.
  • Deal A; Human Vaccine Institute, Duke University School of Medicine, Durham, North Carolina, USA.
  • Edwards RW; Department of Surgery, Duke University School of Medicine, Durham, North Carolina, USA.
  • Tegha G; The University of North Carolina Project, Lilongwe, Malawi.
  • Kamwendo D; The University of North Carolina Project, Lilongwe, Malawi.
  • Kumwenda J; The University of North Carolina Project, Lilongwe, Malawi.
  • Nelson JA; Department of Microbiology and Immunology, University of North Carolina School of Medicine, Chapel Hill, North Carolina, USA.
  • Liao HX; Human Vaccine Institute, Duke University School of Medicine, Durham, North Carolina, USA.
  • Brinkley C; Human Vaccine Institute, Duke University School of Medicine, Durham, North Carolina, USA.
  • Denny TN; Human Vaccine Institute, Duke University School of Medicine, Durham, North Carolina, USA.
  • Ochsenbauer C; Department of Medicine, University of Alabama at Birmingham, Birmingham, Alabama, USA.
  • Ellington S; Division of Reproductive Health, National Center for Chronic Disease Prevention and Health Promotion, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
  • King CC; Division of Reproductive Health, National Center for Chronic Disease Prevention and Health Promotion, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
  • Jamieson DJ; Division of Reproductive Health, National Center for Chronic Disease Prevention and Health Promotion, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
  • van der Horst C; Division of Infectious Diseases, University of North Carolina School of Medicine, Chapel Hill, North Carolina, USA.
  • Kourtis AP; Division of Reproductive Health, National Center for Chronic Disease Prevention and Health Promotion, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
  • Tomaras GD; Human Vaccine Institute, Duke University School of Medicine, Durham, North Carolina, USA.
  • Ferrari G; Department of Surgery, Duke University School of Medicine, Durham, North Carolina, USA.
  • Permar SR; Human Vaccine Institute, Duke University School of Medicine, Durham, North Carolina, USA sallie.permar@dm.duke.edu.
J Virol ; 89(19): 9952-61, 2015 Oct.
Article em En | MEDLINE | ID: mdl-26202232
ABSTRACT
UNLABELLED Infants born to HIV-1-infected mothers in resource-limited areas where replacement feeding is unsafe and impractical are repeatedly exposed to HIV-1 throughout breastfeeding. Despite this, the majority of infants do not contract HIV-1 postnatally, even in the absence of maternal antiretroviral therapy. This suggests that immune factors in breast milk of HIV-1-infected mothers help to limit vertical transmission. We compared the HIV-1 envelope-specific breast milk and plasma antibody responses of clade C HIV-1-infected postnatally transmitting and nontransmitting mothers in the control arm of the Malawi-based Breastfeeding Antiretrovirals and Nutrition Study using multivariable logistic regression modeling. We found no association between milk or plasma neutralization activity, antibody-dependent cell-mediated cytotoxicity, or HIV-1 envelope-specific IgG responses and postnatal transmission risk. While the envelope-specific breast milk and plasma IgA responses also did not reach significance in predicting postnatal transmission risk in the primary model after correction for multiple comparisons, subsequent exploratory analysis using two distinct assay methodologies demonstrated that the magnitudes of breast milk total and secretory IgA responses against a consensus HIV-1 envelope gp140 (B.con env03) were associated with reduced postnatal transmission risk. These results suggest a protective role for mucosal HIV-1 envelope-specific IgA responses in the context of postnatal virus transmission. This finding supports further investigations into the mechanisms by which mucosal IgA reduces risk of HIV-1 transmission via breast milk and into immune interventions aimed at enhancing this response. IMPORTANCE Infants born to HIV-1-infected mothers are repeatedly exposed to the virus in breast milk. Remarkably, the transmission rate is low, suggesting that immune factors in the breast milk of HIV-1-infected mothers help to limit transmission. We compared the antibody responses in plasma and breast milk of HIV-1-transmitting and -nontransmitting mothers to identify responses that correlated with reduced risk of postnatal HIV-1 transmission. We found that neither plasma nor breast milk IgG antibody responses were associated with risk of HIV-1 transmission. In contrast, the magnitudes of the breast milk IgA and secretory IgA responses against HIV-1 envelope proteins were associated with reduced risk of postnatal HIV-1 transmission. The results of this study support further investigations of the mechanisms by which mucosal IgA may reduce the risk of HIV-1 transmission via breastfeeding and the development of strategies to enhance milk envelope-specific IgA responses to reduce mother-to-child HIV transmission and promote an HIV-free generation.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Contexto em Saúde: 2_ODS3 Problema de saúde: 2_enfermedades_transmissibles Assunto principal: Imunoglobulina A / Anticorpos Anti-HIV / Infecções por HIV / HIV-1 / Transmissão Vertical de Doenças Infecciosas / Leite Humano Tipo de estudo: Clinical_trials / Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Infant / Newborn / Pregnancy País/Região como assunto: Africa Idioma: En Revista: J Virol Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Contexto em Saúde: 2_ODS3 Problema de saúde: 2_enfermedades_transmissibles Assunto principal: Imunoglobulina A / Anticorpos Anti-HIV / Infecções por HIV / HIV-1 / Transmissão Vertical de Doenças Infecciosas / Leite Humano Tipo de estudo: Clinical_trials / Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Infant / Newborn / Pregnancy País/Região como assunto: Africa Idioma: En Revista: J Virol Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Estados Unidos
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