4.7 Article

Effect of Immune-Enhancing Enteral Nutrition Enriched with or without Beta-Glucan on Immunomodulation in Critically III Patients

期刊

NUTRIENTS
卷 8, 期 6, 页码 -

出版社

MDPI
DOI: 10.3390/nu8060336

关键词

beta-glucan; enteral nutrition; ICU; NK cell; immune system; inflammation

资金

  1. Bio-Synergy Research Project of the Ministry of Science, ICT and Future Planning through the National Research Foundation, Republic of Korea [NRF-2012M3A9C4048762]
  2. Ministry of Trade, Industry, and Energy (MOTIE)
  3. Korea Institute for Advancement of Technology (KIAT) through Promoting Regional Specialized Industry
  4. Cooperative Research Program for Agriculture Science & Technology Development, Rural Development Administration, Republic of Korea [PJ010835]

向作者/读者索取更多资源

We investigated whether high-protein enteral nutrition with immune-modulating nutrients (IMHP) enriched with beta-glucan stimulates immune function in critically ill patients. In a randomized double-blind placebo-controlled study, 30 patients consumed one of three types of enteral nutrition: a control or IMHP with and without beta-glucan. The IMHP with beta-glucan group showed increases in natural killer (NK) cell activities relative to the baseline, and greater increases were observed in NK cell activities relative to the control group after adjusting for age and gender. The IMHP groups with and without beta-glucan had greater increases in serum prealbumin and decreases in high-sensitivity C-reactive protein (hs-CRP) than the control group. The control group had a greater decrease in peripheral blood mononuclear cell (PBMC) interleukin (IL)-12 production than the IMHP with and without beta-glucan groups. In all patients, the change (Delta) in hs-CRP was correlated with A prealbumin and A PBMC IL-12, which were correlated with Delta NK cell activity and Delta prealbumin. This study showed beneficial effects of a combination treatment of beta-glucan and IMHP on NK cell activity. Additionally, strong correlations among changes in NK cell activity, PBMC IL-12, and hs-CRP suggested that beta-glucan could be an attractive candidate for stimulating protective immunity without enhanced inflammation (ClinicalTrials.gov: NCT02569203).

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