Abstract
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.
AimTo investigate the effects of COL supplementation on in vivo immunity following prolonged exercise using experimental contact hypersensitivity (CHS) with the novel antigen Diphenylcyclopropenone (DPCP).
MethodsIn 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 h 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).
ResultsThere was no difference in summed skinfold thickness responses between COL and PLA (p > 0.05). However, sensitivity of in vivo immune responsiveness was greater with COL at 24 h (p < 0.001) and 48 h (p < 0.05) with doses ~2-fold greater required to elicit a positive response in PLA.
ConclusionsCOL 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 previous studies. These findings also suggest that CHS sensitivity is highly relevant to host defence and in vivo protection against infection.
AimTo investigate the effects of COL supplementation on in vivo immunity following prolonged exercise using experimental contact hypersensitivity (CHS) with the novel antigen Diphenylcyclopropenone (DPCP).
MethodsIn 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 h 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).
ResultsThere was no difference in summed skinfold thickness responses between COL and PLA (p > 0.05). However, sensitivity of in vivo immune responsiveness was greater with COL at 24 h (p < 0.001) and 48 h (p < 0.05) with doses ~2-fold greater required to elicit a positive response in PLA.
ConclusionsCOL 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 previous studies. These findings also suggest that CHS sensitivity is highly relevant to host defence and in vivo protection against infection.
Original language | English |
---|---|
Pages (from-to) | 335-344 |
Number of pages | 10 |
Journal | European Journal of Nutrition |
Volume | 58 |
Issue number | 1 |
Early online date | 22 Dec 2017 |
DOIs | |
Publication status | Published - 01 Feb 2019 |
Keywords
- running
- host defence
- contact hypersensitivity
- diphenylcyclopropenone
- whole integrated immune response