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Systemic immune changes following meal intake in humans
K Hansen1, F Sickelmann, R Pietrowsky
1Department of Internal Medicine, University of Lübeck, Germany.
The American Journal of Physiology
|August 1, 1997
Summary
A high-protein meal alters immune cell distribution and cytokine production in healthy men. This meal intake increased neutrophils and platelets while decreasing lymphocytes and interferon-gamma (IFN-γ) production.
Area of Science:
- Immunology
- Nutrition Science
- Human Physiology
Background:
- Food intake presents a significant intestinal antigen exposure, necessitating robust host defense mechanisms.
- Both local immune activation and coordinated systemic immune responses are crucial for managing dietary antigens.
- The systemic immune response may play a supportive role in bolstering local intestinal immunity.
Purpose of the Study:
- To investigate the systemic immune response following the consumption of a standardized high-protein meal.
- To assess the impact of a high-protein meal on peripheral blood mononuclear cell counts.
- To evaluate changes in cytokine production (TNF-α, IL-1β, IL-6, IFN-γ) and plasma hormone levels (cortisol, growth hormone).
Main Methods:
- A controlled study involving ten healthy men aged 18-35 years.
- Two experimental sessions: one fasting and one post-high-protein meal.
- Frequent blood sampling (every 15 min) to analyze cell counts, cytokine levels, and hormone concentrations.
Main Results:
- Postprandial increase in neutrophil and platelet counts lasting over 2.5 hours.
- Significant decrease in lymphocyte counts following meal intake.
- Reduced in vitro production of interferon-gamma (IFN-γ) after the meal.
- Elevated plasma cortisol concentrations observed post-meal.
- No significant changes in TNF-α, IL-1β, or IL-6 production or plasma levels.
Conclusions:
- A high-protein meal induces significant systemic immune changes, including altered leukocyte distribution and reduced IFN-γ production.
- These immune alterations are associated with a postprandial increase in plasma cortisol levels.
- The observed changes, such as lymphocyte emigration, may contribute to supporting local intestinal immune defense mechanisms.