An expert panel on the adequacy of safety data and physiological roles of dietary bovine osteopontin in infancy

Human milk, due to its unique composition, is the optimal standard for infant nutrition. Osteopontin (OPN) is abundant in human milk but not bovine milk. The addition of bovine milk osteopontin (bmOPN) to formula may replicate OPN’s concentration and function in human milk. To address safety concern...

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发表在:Frontiers in Nutrition
Main Authors: Stephen A. Fleming, Sarah M. Reyes, Sharon M. Donovan, Olle Hernell, Rulan Jiang, Bo Lönnerdal, Josef Neu, Lawrence Steinman, Esben S. Sørensen, Christina E. West, Ronald Kleinman, John C. Wallingford
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语言:英语
出版: Frontiers Media S.A. 2024-06-01
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在线阅读:https://www.frontiersin.org/articles/10.3389/fnut.2024.1404303/full
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author Stephen A. Fleming
Sarah M. Reyes
Sharon M. Donovan
Olle Hernell
Rulan Jiang
Bo Lönnerdal
Josef Neu
Lawrence Steinman
Esben S. Sørensen
Christina E. West
Ronald Kleinman
Ronald Kleinman
John C. Wallingford
author_facet Stephen A. Fleming
Sarah M. Reyes
Sharon M. Donovan
Olle Hernell
Rulan Jiang
Bo Lönnerdal
Josef Neu
Lawrence Steinman
Esben S. Sørensen
Christina E. West
Ronald Kleinman
Ronald Kleinman
John C. Wallingford
author_sort Stephen A. Fleming
collection DOAJ
container_title Frontiers in Nutrition
description Human milk, due to its unique composition, is the optimal standard for infant nutrition. Osteopontin (OPN) is abundant in human milk but not bovine milk. The addition of bovine milk osteopontin (bmOPN) to formula may replicate OPN’s concentration and function in human milk. To address safety concerns, we convened an expert panel to assess the adequacy of safety data and physiological roles of dietary bmOPN in infancy. The exposure of breastfed infants to human milk OPN (hmOPN) has been well-characterized and decreases markedly over the first 6 months of lactation. Dietary bmOPN is resistant to gastric and intestinal digestion, absorbed and cleared from circulation within 8–24 h, and represents a small portion (<5%) of total plasma OPN. Label studies on hmOPN suggest that after 3 h, intact or digested OPN is absorbed into carcass (62%), small intestine (23%), stomach (5%), and small intestinal perfusate (4%), with <2% each found in the cecum, liver, brain, heart, and spleen. Although the results are heterogenous with respect to bmOPN’s physiologic impact, no adverse impacts have been reported across growth, gastrointestinal, immune, or brain-related outcomes. Recombinant bovine and human forms demonstrate similar absorption in plasma as bmOPN, as well as effects on cognition and immunity. The panel recommended prioritization of trials measuring a comprehensive set of clinically relevant outcomes on immunity and cognition to confirm the safety of bmOPN over that of further research on its absorption, distribution, metabolism, and excretion. This review offers expert consensus on the adequacy of data available to assess the safety of bmOPN for use in infant formula, aiding evidence-based decisions on the formulation of infant formula.
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spelling doaj-art-eed2ae986a36498689796d737fbbeba82025-08-19T23:14:58ZengFrontiers Media S.A.Frontiers in Nutrition2296-861X2024-06-011110.3389/fnut.2024.14043031404303An expert panel on the adequacy of safety data and physiological roles of dietary bovine osteopontin in infancyStephen A. Fleming0Sarah M. Reyes1Sharon M. Donovan2Olle Hernell3Rulan Jiang4Bo Lönnerdal5Josef Neu6Lawrence Steinman7Esben S. Sørensen8Christina E. West9Ronald Kleinman10Ronald Kleinman11John C. Wallingford12Traverse Science, Inc., Mundelein, IL, United StatesRev Bioscience, LLC, Boise, ID, United StatesDepartment of Food Science and Human Nutrition, University of Illinois Urbana-Champaign, Urbana, IL, United StatesDepartment of Clinical Sciences and Pediatrics, Umeå University, Umeå, SwedenDepartment of Nutrition, University of California, Davis, Davis, CA, United StatesDepartment of Nutrition, University of California, Davis, Davis, CA, United StatesDepartment of Pediatrics, Division of Neonatology, University of Florida, Gainesville, FL, United StatesDepartments of Pediatrics and of Neurology and Neurological Sciences, Interdepartmental Program in Immunology, Beckman Center for Molecular Medicine, Stanford University School of Medicine, Stanford, CA, United StatesDepartment of Molecular Biology and Genetics, Aarhus University, Aarhus, DenmarkDepartment of Clinical Sciences and Pediatrics, Umeå University, Umeå, SwedenHarvard Medical School, Boston, MA, United States0Department of Pediatrics, Massachusetts General Hospital, Boston, MA, United States1Nutrispectives, LLC, Spokane, WA, United StatesHuman milk, due to its unique composition, is the optimal standard for infant nutrition. Osteopontin (OPN) is abundant in human milk but not bovine milk. The addition of bovine milk osteopontin (bmOPN) to formula may replicate OPN’s concentration and function in human milk. To address safety concerns, we convened an expert panel to assess the adequacy of safety data and physiological roles of dietary bmOPN in infancy. The exposure of breastfed infants to human milk OPN (hmOPN) has been well-characterized and decreases markedly over the first 6 months of lactation. Dietary bmOPN is resistant to gastric and intestinal digestion, absorbed and cleared from circulation within 8–24 h, and represents a small portion (<5%) of total plasma OPN. Label studies on hmOPN suggest that after 3 h, intact or digested OPN is absorbed into carcass (62%), small intestine (23%), stomach (5%), and small intestinal perfusate (4%), with <2% each found in the cecum, liver, brain, heart, and spleen. Although the results are heterogenous with respect to bmOPN’s physiologic impact, no adverse impacts have been reported across growth, gastrointestinal, immune, or brain-related outcomes. Recombinant bovine and human forms demonstrate similar absorption in plasma as bmOPN, as well as effects on cognition and immunity. The panel recommended prioritization of trials measuring a comprehensive set of clinically relevant outcomes on immunity and cognition to confirm the safety of bmOPN over that of further research on its absorption, distribution, metabolism, and excretion. This review offers expert consensus on the adequacy of data available to assess the safety of bmOPN for use in infant formula, aiding evidence-based decisions on the formulation of infant formula.https://www.frontiersin.org/articles/10.3389/fnut.2024.1404303/fullinfantmilkosteopontinsafetyimmunityneurodevelopment
spellingShingle Stephen A. Fleming
Sarah M. Reyes
Sharon M. Donovan
Olle Hernell
Rulan Jiang
Bo Lönnerdal
Josef Neu
Lawrence Steinman
Esben S. Sørensen
Christina E. West
Ronald Kleinman
Ronald Kleinman
John C. Wallingford
An expert panel on the adequacy of safety data and physiological roles of dietary bovine osteopontin in infancy
infant
milk
osteopontin
safety
immunity
neurodevelopment
title An expert panel on the adequacy of safety data and physiological roles of dietary bovine osteopontin in infancy
title_full An expert panel on the adequacy of safety data and physiological roles of dietary bovine osteopontin in infancy
title_fullStr An expert panel on the adequacy of safety data and physiological roles of dietary bovine osteopontin in infancy
title_full_unstemmed An expert panel on the adequacy of safety data and physiological roles of dietary bovine osteopontin in infancy
title_short An expert panel on the adequacy of safety data and physiological roles of dietary bovine osteopontin in infancy
title_sort expert panel on the adequacy of safety data and physiological roles of dietary bovine osteopontin in infancy
topic infant
milk
osteopontin
safety
immunity
neurodevelopment
url https://www.frontiersin.org/articles/10.3389/fnut.2024.1404303/full
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