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The effects of bovine colostrum supplementation on in vivo immunity following prolonged exercise: a randomised controlled trial

BACKGROUND: Bovine colostrum (COL) has been advocated as a nutritional countermeasure to exercise-induced immune dysfunction, but there is a lack of research with clinically relevant in vivo measures. AIM: To investigate the effects of COL supplementation on in vivo immunity following prolonged exer...

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Autores principales: Jones, A. W., March, D. S., Thatcher, R., Diment, B., Walsh, N. P., Davison, Glen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6425115/
https://www.ncbi.nlm.nih.gov/pubmed/29274034
http://dx.doi.org/10.1007/s00394-017-1597-6
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author Jones, A. W.
March, D. S.
Thatcher, R.
Diment, B.
Walsh, N. P.
Davison, Glen
author_facet Jones, A. W.
March, D. S.
Thatcher, R.
Diment, B.
Walsh, N. P.
Davison, Glen
author_sort Jones, A. W.
collection PubMed
description BACKGROUND: Bovine colostrum (COL) has been advocated as a nutritional countermeasure to exercise-induced immune dysfunction, but there is a lack of research with clinically relevant in vivo measures. AIM: To investigate the effects of COL supplementation on in vivo immunity following prolonged exercise using experimental contact hypersensitivity (CHS) with the novel antigen diphenylcyclopropenone (DPCP). METHODS: In a double-blind design, 31 men were randomly assigned to COL (20 g/day) or placebo (PLA) for 58 days. Participants ran for 2 h at 60% maximal aerobic capacity on day 28 and received a primary DPCP exposure (sensitisation) 20 min after. On day 56, participants received a low-dose-series DPCP challenge to elicit recall of in vivo immune-specific memory (quantified by skinfold thickness 24 and 48 h later). Analysis of the dose–response curves allowed determination of the minimum dose required to elicit a positive response (i.e., sensitivity). RESULTS: There was no difference in summed skinfold thickness responses between COL and PLA at 24 h (p = 0.124) and 48 h (p = 0.405). However, sensitivity of in vivo immune responsiveness was greater with COL at 24 h (p < 0.001) and 48 h (p = 0.023) with doses ~ twofold greater required to elicit a positive response in PLA. CONCLUSIONS: COL blunts the prolonged exercise-induced decrease in clinically relevant in vivo immune responsiveness to a novel antigen, which may be a mechanism for reduced illness reports observed in the previous studies. These findings also suggest that CHS sensitivity is highly relevant to host defence.
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spelling pubmed-64251152019-04-05 The effects of bovine colostrum supplementation on in vivo immunity following prolonged exercise: a randomised controlled trial Jones, A. W. March, D. S. Thatcher, R. Diment, B. Walsh, N. P. Davison, Glen Eur J Nutr Original Contribution BACKGROUND: Bovine colostrum (COL) has been advocated as a nutritional countermeasure to exercise-induced immune dysfunction, but there is a lack of research with clinically relevant in vivo measures. AIM: To investigate the effects of COL supplementation on in vivo immunity following prolonged exercise using experimental contact hypersensitivity (CHS) with the novel antigen diphenylcyclopropenone (DPCP). METHODS: In a double-blind design, 31 men were randomly assigned to COL (20 g/day) or placebo (PLA) for 58 days. Participants ran for 2 h at 60% maximal aerobic capacity on day 28 and received a primary DPCP exposure (sensitisation) 20 min after. On day 56, participants received a low-dose-series DPCP challenge to elicit recall of in vivo immune-specific memory (quantified by skinfold thickness 24 and 48 h later). Analysis of the dose–response curves allowed determination of the minimum dose required to elicit a positive response (i.e., sensitivity). RESULTS: There was no difference in summed skinfold thickness responses between COL and PLA at 24 h (p = 0.124) and 48 h (p = 0.405). However, sensitivity of in vivo immune responsiveness was greater with COL at 24 h (p < 0.001) and 48 h (p = 0.023) with doses ~ twofold greater required to elicit a positive response in PLA. CONCLUSIONS: COL blunts the prolonged exercise-induced decrease in clinically relevant in vivo immune responsiveness to a novel antigen, which may be a mechanism for reduced illness reports observed in the previous studies. These findings also suggest that CHS sensitivity is highly relevant to host defence. Springer Berlin Heidelberg 2017-12-22 2019 /pmc/articles/PMC6425115/ /pubmed/29274034 http://dx.doi.org/10.1007/s00394-017-1597-6 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Contribution
Jones, A. W.
March, D. S.
Thatcher, R.
Diment, B.
Walsh, N. P.
Davison, Glen
The effects of bovine colostrum supplementation on in vivo immunity following prolonged exercise: a randomised controlled trial
title The effects of bovine colostrum supplementation on in vivo immunity following prolonged exercise: a randomised controlled trial
title_full The effects of bovine colostrum supplementation on in vivo immunity following prolonged exercise: a randomised controlled trial
title_fullStr The effects of bovine colostrum supplementation on in vivo immunity following prolonged exercise: a randomised controlled trial
title_full_unstemmed The effects of bovine colostrum supplementation on in vivo immunity following prolonged exercise: a randomised controlled trial
title_short The effects of bovine colostrum supplementation on in vivo immunity following prolonged exercise: a randomised controlled trial
title_sort effects of bovine colostrum supplementation on in vivo immunity following prolonged exercise: a randomised controlled trial
topic Original Contribution
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6425115/
https://www.ncbi.nlm.nih.gov/pubmed/29274034
http://dx.doi.org/10.1007/s00394-017-1597-6
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