Abstract
Background and aims: The immune mechanisms by which probiotics reduce susceptibility to upper respiratory tract illness is uncertain. The aim of this study was to examine purported cell-mediated immune mechanisms that might explain the reduction in respiratory illness observed following daily supplementation with Bifidobacterium animalis subsp. lactis Bl-04 (Bl-04) and a combined Lactobacillus acidophilus NCFM & B. animalis subsp. lactis BI-07 (NCFM & Bi-07). Methods: A cohort of 144 healthy physically active individuals were allocated to daily supplementation consumed as a beverage with Bl-04 (n=46) supplemented at a dosage of 2.0×109 colony forming units (cfu) per day, NCFM & Bi-07 (n=47) at a dosage of 5.0×109CFU per day each, or a placebo (n=51) over 150d. Markers included plasma cytokines, metalloproteinases and neurotrophins, peripheral blood leucocyte numbers, antibody-dependent and antibody-independent NK cell activity (NKCA), and peripheral blood mononuclear cell (PBMC) phagocytosis. Results: A total of 125 subjects were included in the final analysis. No significant effects were observed on cytokines, on white cell differentials, NKCA or PBMC phagocytosis from pre- to post-supplementation. The biomarkers that increased significantly from pre- to post-supplementation were the concentration of plasma macrophage inflammatory protein (MIP)-1δ which was higher in the Bl-04 than placebo group (Bl-04 25%±11%, placebo-3.3%±9.4%; mean±SD, P=0.003) while the concentration of plasma matrix metallo-proteinase (MMP)-1 decreased by 11%±16% in the NCFM & Bi-07 group and increased by 21%±17% in the placebo group, which was a significant 26% difference (8-41%; P=0.02). Conclusion: Probiotic supplementation had little effect on parameters of the innate immune system. Mechanisms explaining the beneficial effect of Bl-04 or NCFM & Bi-07 supplementation on respiratory illness remain unclear.
Original language | English |
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Pages (from-to) | 178-184 |
Number of pages | 7 |
Journal | e-SPEN Journal |
Volume | 9 |
Issue number | 5 |
DOIs | |
Publication status | Published - 2014 |
Externally published | Yes |