Journal
EUROPEAN JOURNAL OF CLINICAL NUTRITION
Volume 64, Issue 7, Pages 720-726Publisher
NATURE PUBLISHING GROUP
DOI: 10.1038/ejcn.2010.32
Keywords
Agaricus bisporus; alpha-glucan; cytokines; immune modulation; nutrition; peripheral mononuclear blood cell
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Funding
- Innerlife (Venlo, the Netherlands)
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Introduction: Mushrooms are known for their immune modulating effect for which the polysaccharide fraction, mainly glucans, seem to be responsible. Fungal beta-glucans have been studied extensively, whereas little is known about mushroom alpha-glucans. We have earlier shown that the polysaccharide fraction from the mushroom A. bisporus, consisting 90% of alpha-glucans, induced in vitro tumor necrosis factor (TNF)alpha and nitric oxide production. The purpose of this study was to evaluate the effects of consuming. Method: A. bisporus alpha-glucan on ex vivo cytokine production by human peripheral mononuclear blood cells (PBMCs). A doubleblind randomized trial was designed in which 56 mildly hypercholesterolemic subjects consumed a control fruit juice with no added alpha-glucans (200 ml/day) for a 2-week run-in period. For the next 5 weeks, the control group (N 30) continued consumption of the control fruit juice, whereas the intervention group (N 26) consumed the same fruit juice enriched with alpha-glucans from A. bisporus (5 g glucans/day). Changes in interleukin (IL)-1 beta, IL-6 and TNF alpha cytokine production by lipopolysaccharide (LPS)-stimulated PBMCs were evaluated, as well as changes in T-helper (Th)1/Th2 cytokines by phytohemaggutinin (PHA)-stimulated PBMCs. Results: Consumption of A. bisporus alpha-glucans lower LPS-induced TNF alpha production by 69% (P 0.017) as compared with the control group, whereas no effect on IL-1b and IL-6 was observed. No obvious Th1 -Th2 skewing by PHA-stimulated PBMCs was observed. However, we observed a trend towards a decreased production of IL-12 and IL-10. Conclusion: Our current finding suggests that in vivo, alpha-glucans have lost their efficacy to stimulate the immune response as observed in our in vitro mouse model. European Journal of Clinical Nutrition (2010) 64, 720 -726; doi: 10.1038/ejcn. 2010.32; published online 3 March 2010
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