Human Milk and Allergic Diseases: An Unsolved Puzzle
There is conflicting evidence on the protective role of breastfeeding in relation to the development of allergic sensitisation and allergic disease. Studies vary in methodology and definition of outcomes, which lead to considerable heterogeneity. Human milk composition varies both within and between...
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Published in | Nutrients Vol. 9; no. 8; p. 894 |
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Main Authors | , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
MDPI AG
17.08.2017
MDPI |
Subjects | |
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Abstract | There is conflicting evidence on the protective role of breastfeeding in relation to the development of allergic sensitisation and allergic disease. Studies vary in methodology and definition of outcomes, which lead to considerable heterogeneity. Human milk composition varies both within and between individuals, which may partially explain conflicting data. It is known that human milk composition is very complex and contains variable levels of immune active molecules, oligosaccharides, metabolites, vitamins and other nutrients and microbial content. Existing evidence suggests that modulation of human breast milk composition has potential for preventing allergic diseases in early life. In this review, we discuss associations between breastfeeding/human milk composition and allergy development. |
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AbstractList | There is conflicting evidence on the protective role of breastfeeding in relation to the development of allergic sensitisation and allergic disease. Studies vary in methodology and definition of outcomes, which lead to considerable heterogeneity. Human milk composition varies both within and between individuals, which may partially explain conflicting data. It is known that human milk composition is very complex and contains variable levels of immune active molecules, oligosaccharides, metabolites, vitamins and other nutrients and microbial content. Existing evidence suggests that modulation of human breast milk composition has potential for preventing allergic diseases in early life. In this review, we discuss associations between breastfeeding/human milk composition and allergy development. There is conflicting evidence on the protective role of breastfeeding in relation to the development of allergic sensitisation and allergic disease. Studies vary in methodology and definition of outcomes, which lead to considerable heterogeneity. Human milk composition varies both within and between individuals, which may partially explain conflicting data. It is known that human milk composition is very complex and contains variable levels of immune active molecules, oligosaccharides, metabolites, vitamins and other nutrients and microbial content. Existing evidence suggests that modulation of human breast milk composition has potential for preventing allergic diseases in early life. In this review, we discuss associations between breastfeeding/human milk composition and allergy development.There is conflicting evidence on the protective role of breastfeeding in relation to the development of allergic sensitisation and allergic disease. Studies vary in methodology and definition of outcomes, which lead to considerable heterogeneity. Human milk composition varies both within and between individuals, which may partially explain conflicting data. It is known that human milk composition is very complex and contains variable levels of immune active molecules, oligosaccharides, metabolites, vitamins and other nutrients and microbial content. Existing evidence suggests that modulation of human breast milk composition has potential for preventing allergic diseases in early life. In this review, we discuss associations between breastfeeding/human milk composition and allergy development. |
Author | Wegienka, Ganesa Gay, Melvin Land, Belinda Kolotilina, Anastasia Garssen, Johan Warner, John Boix-Amorós, Alba Boyle, Robert Kozyrskyj, Anita Geddes, Donna Peroni, Diego Collado, Maria Slupsky, Carolyn Munblit, Daniel Skevaki, Chrysanthi Hsu, Peter Nanan, Ralph |
AuthorAffiliation | 4 Department of Clinical and Experimental Medicine, Section of Paediatrics, University of Pisa, 56126 Pisa, Italy 7 Nutricia Research, 3584 CT Utrecht, The Netherlands; Belinda.vantland@danone.com (B.V.L.); johan.garssen@danone.com (J.G.) 8 Department of Paediatric Immunology, Wilhelmina Children’s Hospital, University Medical Centre Utrecht, 3584 EA Utrecht, The Netherlands 12 Charles Perkins Centre Nepean, University of Sydney, Sydney, NSW 2747, Australia; ralph.nanan@sydney.edu.au 1 Department of Paediatrics, Imperial College London, London W2 1NY, UK; r.boyle@nhs.net (R.J.B.); j.o.warner@imperial.ac.uk (J.O.W.) 3 The In-FLAME Global Network, an Affiliate of the World Universities Network (WUN), West New York, NJ 07093, USA; diego.peroni@unipi.it (D.G.P.); albaboix90@gmail.com (A.B.-A.); peter.hsu@health.nsw.gov.au (P.S.H.); melvin.gay@uwa.edu.au (M.C.L.G.); Chrysanthi.Skevaki@uk-gm.de (C.S.); mcolam@iata.csic.es (M.C.C.); Donna.Geddes@uwa.edu.au (D.T.G.); gwegien1@hfhs.org (G.W.) 13 Depa |
AuthorAffiliation_xml | – name: 3 The In-FLAME Global Network, an Affiliate of the World Universities Network (WUN), West New York, NJ 07093, USA; diego.peroni@unipi.it (D.G.P.); albaboix90@gmail.com (A.B.-A.); peter.hsu@health.nsw.gov.au (P.S.H.); melvin.gay@uwa.edu.au (M.C.L.G.); Chrysanthi.Skevaki@uk-gm.de (C.S.); mcolam@iata.csic.es (M.C.C.); Donna.Geddes@uwa.edu.au (D.T.G.); gwegien1@hfhs.org (G.W.) – name: 13 Department of Nutrition, University of California, Davis, CA 95616-5270, USA; cslupsky@ucdavis.edu – name: 17 National Institute for Health Research, Collaboration for Leadership in Applied Health Research and Care for NW London, London SW10 9NH, UK – name: 4 Department of Clinical and Experimental Medicine, Section of Paediatrics, University of Pisa, 56126 Pisa, Italy – name: 11 Utrecht Institute for Pharmaceutical Sciences, Faculty of Science, Utrecht University, 3584 CG Utrecht, The Netherlands – name: 15 Center for Urban Responses to Environmental Stressors, Detroit, MI 48202, USA – name: 8 Department of Paediatric Immunology, Wilhelmina Children’s Hospital, University Medical Centre Utrecht, 3584 EA Utrecht, The Netherlands – name: 1 Department of Paediatrics, Imperial College London, London W2 1NY, UK; r.boyle@nhs.net (R.J.B.); j.o.warner@imperial.ac.uk (J.O.W.) – name: 2 Faculty of Pediatrics, I.M. Sechenov First Moscow State Medical University, 119991 Moscow, Russia; aikolotilina@yandex.ru – name: 7 Nutricia Research, 3584 CT Utrecht, The Netherlands; Belinda.vantland@danone.com (B.V.L.); johan.garssen@danone.com (J.G.) – name: 9 School of Molecular Sciences, The University of Western Australia, Perth, WA 6009, Australia – name: 12 Charles Perkins Centre Nepean, University of Sydney, Sydney, NSW 2747, Australia; ralph.nanan@sydney.edu.au – name: 14 Department of Public Health Sciences, Henry Ford Health System, Detroit, MI 48202, USA – name: 10 Institute of Laboratory Medicine and Pathobiochemistry, Molecular Diagnostics, Philipps University Marburg, University Hospital Giessen and Marburg GmbH Baldingerstr, 35043 Marburg, Germany – name: 5 Institute of Agrochemistry and Food Technology, National Research Council (IATA-CSIC), 46980 Valencia, Spain – name: 6 Allergy and Immunology, The Kids Research Institute, The Children’s Hospital at Westmead, Sydney, NSW 2145, Australia – name: 16 Department of Pediatrics, University of Alberta, Edmonton, AB T6G 1C9, Canada; kozyrsky@ualberta.ca |
Author_xml | – sequence: 1 givenname: Daniel orcidid: 0000-0001-9652-6856 surname: Munblit fullname: Munblit, Daniel – sequence: 2 givenname: Diego orcidid: 0000-0002-0234-1373 surname: Peroni fullname: Peroni, Diego – sequence: 3 givenname: Alba surname: Boix-Amorós fullname: Boix-Amorós, Alba – sequence: 4 givenname: Peter surname: Hsu fullname: Hsu, Peter – sequence: 5 givenname: Belinda surname: Land fullname: Land, Belinda – sequence: 6 givenname: Melvin orcidid: 0000-0003-2581-4556 surname: Gay fullname: Gay, Melvin – sequence: 7 givenname: Anastasia orcidid: 0000-0003-1299-2134 surname: Kolotilina fullname: Kolotilina, Anastasia – sequence: 8 givenname: Chrysanthi surname: Skevaki fullname: Skevaki, Chrysanthi – sequence: 9 givenname: Robert orcidid: 0000-0002-4913-7580 surname: Boyle fullname: Boyle, Robert – sequence: 10 givenname: Maria orcidid: 0000-0002-6204-4864 surname: Collado fullname: Collado, Maria – sequence: 11 givenname: Johan surname: Garssen fullname: Garssen, Johan – sequence: 12 givenname: Donna surname: Geddes fullname: Geddes, Donna – sequence: 13 givenname: Ralph surname: Nanan fullname: Nanan, Ralph – sequence: 14 givenname: Carolyn surname: Slupsky fullname: Slupsky, Carolyn – sequence: 15 givenname: Ganesa surname: Wegienka fullname: Wegienka, Ganesa – sequence: 16 givenname: Anita surname: Kozyrskyj fullname: Kozyrskyj, Anita – sequence: 17 givenname: John surname: Warner fullname: Warner, John |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/28817095$$D View this record in MEDLINE/PubMed |
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Keywords | thymus oligosaccharides allergy cytokines human milk breastfeeding microbiome allergic diseases |
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SubjectTerms | Baby foods Breast Feeding breast milk Breastfeeding & lactation Humans hypersensitivity Hypersensitivity - immunology Hypersensitivity - prevention & control Meta-Analysis as Topic metabolites Microbiota Micronutrients - analysis Milk milk composition Milk, Human - chemistry Milk, Human - microbiology nutrients Observational Studies as Topic oligosaccharides Oligosaccharides - analysis protective effect Randomized Controlled Trials as Topic Review vitamins |
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Title | Human Milk and Allergic Diseases: An Unsolved Puzzle |
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