Cargando…

Breastfeeding Behaviors and the Innate Immune System of Human Milk: Working Together to Protect Infants against Inflammation, HIV-1, and Other Infections

The majority of infants’ breastfeeding from their HIV-infected mothers do not acquire HIV-1 infection despite exposure to cell-free virus and cell-associated virus in HIV-infected breast milk. Paradoxically, exclusive breastfeeding regardless of the HIV status of the mother has led to a significant...

Descripción completa

Detalles Bibliográficos
Autores principales: Henrick, Bethany M., Yao, Xiao-Dan, Nasser, Laila, Roozrogousheh, Ava, Rosenthal, Kenneth L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5712557/
https://www.ncbi.nlm.nih.gov/pubmed/29238342
http://dx.doi.org/10.3389/fimmu.2017.01631
_version_ 1783283244169428992
author Henrick, Bethany M.
Yao, Xiao-Dan
Nasser, Laila
Roozrogousheh, Ava
Rosenthal, Kenneth L.
author_facet Henrick, Bethany M.
Yao, Xiao-Dan
Nasser, Laila
Roozrogousheh, Ava
Rosenthal, Kenneth L.
author_sort Henrick, Bethany M.
collection PubMed
description The majority of infants’ breastfeeding from their HIV-infected mothers do not acquire HIV-1 infection despite exposure to cell-free virus and cell-associated virus in HIV-infected breast milk. Paradoxically, exclusive breastfeeding regardless of the HIV status of the mother has led to a significant decrease in mother-to-child transmission (MTCT) compared with non-exclusive breastfeeding. Although it remains unclear how these HIV-exposed infants remain uninfected despite repeated and prolonged exposure to HIV-1, the low rate of transmission is suggestive of a multitude of protective, short-lived bioactive innate immune factors in breast milk. Indeed, recent studies of soluble factors in breast milk shed new light on mechanisms of neonatal HIV-1 protection. This review highlights the role and significance of innate immune factors in HIV-1 susceptibility and infection. Prevention of MTCT of HIV-1 is likely due to multiple factors, including innate immune factors such as lactoferrin and elafin among many others. In pursuing this field, our lab was the first to show that soluble toll-like receptor 2 (sTLR2) directly inhibits HIV infection, integration, and inflammation. More recently, we demonstrated that sTLR2 directly binds to selective HIV-1 proteins, including p17, gp41, and p24, leading to significantly reduced NFκB activation, interleukin-8 production, CCR5 expression, and HIV infection in a dose-dependent manner. Thus, a clearer understanding of soluble milk-derived innate factors with known antiviral functions may provide new therapeutic insights to reduce vertical HIV-1 transmission and will have important implications for protection against HIV-1 infection at other mucosal sites. Furthermore, innate bioactive factors identified in human milk may serve not only in protecting infants against infections and inflammation but also the elderly; thus, opening the door for novel innate immune therapeutics to protect newborns, infants, adults, and the elderly.
format Online
Article
Text
id pubmed-5712557
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-57125572017-12-13 Breastfeeding Behaviors and the Innate Immune System of Human Milk: Working Together to Protect Infants against Inflammation, HIV-1, and Other Infections Henrick, Bethany M. Yao, Xiao-Dan Nasser, Laila Roozrogousheh, Ava Rosenthal, Kenneth L. Front Immunol Immunology The majority of infants’ breastfeeding from their HIV-infected mothers do not acquire HIV-1 infection despite exposure to cell-free virus and cell-associated virus in HIV-infected breast milk. Paradoxically, exclusive breastfeeding regardless of the HIV status of the mother has led to a significant decrease in mother-to-child transmission (MTCT) compared with non-exclusive breastfeeding. Although it remains unclear how these HIV-exposed infants remain uninfected despite repeated and prolonged exposure to HIV-1, the low rate of transmission is suggestive of a multitude of protective, short-lived bioactive innate immune factors in breast milk. Indeed, recent studies of soluble factors in breast milk shed new light on mechanisms of neonatal HIV-1 protection. This review highlights the role and significance of innate immune factors in HIV-1 susceptibility and infection. Prevention of MTCT of HIV-1 is likely due to multiple factors, including innate immune factors such as lactoferrin and elafin among many others. In pursuing this field, our lab was the first to show that soluble toll-like receptor 2 (sTLR2) directly inhibits HIV infection, integration, and inflammation. More recently, we demonstrated that sTLR2 directly binds to selective HIV-1 proteins, including p17, gp41, and p24, leading to significantly reduced NFκB activation, interleukin-8 production, CCR5 expression, and HIV infection in a dose-dependent manner. Thus, a clearer understanding of soluble milk-derived innate factors with known antiviral functions may provide new therapeutic insights to reduce vertical HIV-1 transmission and will have important implications for protection against HIV-1 infection at other mucosal sites. Furthermore, innate bioactive factors identified in human milk may serve not only in protecting infants against infections and inflammation but also the elderly; thus, opening the door for novel innate immune therapeutics to protect newborns, infants, adults, and the elderly. Frontiers Media S.A. 2017-11-29 /pmc/articles/PMC5712557/ /pubmed/29238342 http://dx.doi.org/10.3389/fimmu.2017.01631 Text en Copyright © 2017 Henrick, Yao, Nasser, Roozrogousheh and Rosenthal. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Henrick, Bethany M.
Yao, Xiao-Dan
Nasser, Laila
Roozrogousheh, Ava
Rosenthal, Kenneth L.
Breastfeeding Behaviors and the Innate Immune System of Human Milk: Working Together to Protect Infants against Inflammation, HIV-1, and Other Infections
title Breastfeeding Behaviors and the Innate Immune System of Human Milk: Working Together to Protect Infants against Inflammation, HIV-1, and Other Infections
title_full Breastfeeding Behaviors and the Innate Immune System of Human Milk: Working Together to Protect Infants against Inflammation, HIV-1, and Other Infections
title_fullStr Breastfeeding Behaviors and the Innate Immune System of Human Milk: Working Together to Protect Infants against Inflammation, HIV-1, and Other Infections
title_full_unstemmed Breastfeeding Behaviors and the Innate Immune System of Human Milk: Working Together to Protect Infants against Inflammation, HIV-1, and Other Infections
title_short Breastfeeding Behaviors and the Innate Immune System of Human Milk: Working Together to Protect Infants against Inflammation, HIV-1, and Other Infections
title_sort breastfeeding behaviors and the innate immune system of human milk: working together to protect infants against inflammation, hiv-1, and other infections
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5712557/
https://www.ncbi.nlm.nih.gov/pubmed/29238342
http://dx.doi.org/10.3389/fimmu.2017.01631
work_keys_str_mv AT henrickbethanym breastfeedingbehaviorsandtheinnateimmunesystemofhumanmilkworkingtogethertoprotectinfantsagainstinflammationhiv1andotherinfections
AT yaoxiaodan breastfeedingbehaviorsandtheinnateimmunesystemofhumanmilkworkingtogethertoprotectinfantsagainstinflammationhiv1andotherinfections
AT nasserlaila breastfeedingbehaviorsandtheinnateimmunesystemofhumanmilkworkingtogethertoprotectinfantsagainstinflammationhiv1andotherinfections
AT roozrogoushehava breastfeedingbehaviorsandtheinnateimmunesystemofhumanmilkworkingtogethertoprotectinfantsagainstinflammationhiv1andotherinfections
AT rosenthalkennethl breastfeedingbehaviorsandtheinnateimmunesystemofhumanmilkworkingtogethertoprotectinfantsagainstinflammationhiv1andotherinfections