Effect of Almonds on Immune Strength and Response to Flu Vaccination in Overweight Men
- Conditions
- Immune ResponseInflammation
- Interventions
- Dietary Supplement: Almond groupDietary Supplement: Control Group
- Registration Number
- NCT05031663
- Lead Sponsor
- Loma Linda University
- Brief Summary
This research study will test the effects of almonds on immune functions and immune response to influenza vaccine in overweight middle-aged men
- Detailed Description
The proposed study is a parallel-group, free-living, observer-blind, randomized controlled dietary intervention trial on 54 overweight middle-aged men. This study will be carried out in two phases: Phase 1 will examine the effects of almonds on clinically relevant markers of immune function, and Phase 2 will assess the antibody response to influenza vaccination following almond consumption. Participants will attend a baseline clinic and will be randomized to one of two groups. The Almond group will receive 15% of daily energy intake in the form of almonds as a snack and the Control group will receive an isocaloric carbohydrate-based commercial snack (pretzels). The intervention will be for 12 weeks, at which time both group participants will receive the influenza vaccination, and continue the same dietary intervention for another 16 weeks.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Male
- Target Recruitment
- 61
- Overweight men (Basal Metabolic Index 25-32)
- Age limit between 40-65 years
- Be able to commute to Loma Linda University
- Intolerance or allergy to almonds
- Bad dentures, inability to chew almonds
- Regular intake of almonds and or other nuts
- Use of immune boosting supplements
- Exposure to antibiotics and corticosteroids immediately prior to study
- Have received influenza vaccination in past 10 months
- Uncontrolled chronic disease and psychiatric illness
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Almonds Almond group The almond group will receive 15% of their daily energy intake in the form of almonds Pretzel Control Group The placebo group will receive an isocaloric carbohydrate based pretzel snack
- Primary Outcome Measures
Name Time Method changes in lymphocyte activity and cytokine production baseline to 12 weeks PBMC cells will be separated from blood, activated and cultured using phytohemagglutinin (PHA). Inflammatory cytokine production will be measured in the resulting supernatant using ELISA
changes in complete blood count (CBC) baseline to 12 weeks changes in the complete blood count will be performed on whole blood with the use of an automated hematology analyzer at a certified clinical facility
changes in serum inflammatory cytokine concentration baseline to 12 weeks Changes in the concentrations of the inflammatory cytokines will be performed on serum using enzyme-linked immunoassay (ELISA)
changes in natural killer (NK) cell activity baseline to 12 weeks The NK degranulation assay will be performed on blood samples. The test will be conducted using a modified flow cytometry method that measures the expression of CD107a
changes in lymphocyte populations baseline to 12 weeks Immunophenotyping will be performed by flow cytometry to measure the number of T helper, T cytotoxic, Naïve and memory cells and B cells
changes in the viral load in response to vaccination week 12 to 20 weeks viral load in blood will be measured using a quantitative polymerase chain reaction (qPCR) protocol as described by Ward CL, et al. (2004
changes in neutralizing antibody titers against hemagglutinin and neuraminidase of the vaccine strain week 12 to 20 weeks Neutralizing antibody titers in the serum against the hemagglutinin and neuraminidase of the vaccine strain will be measured using the standard commercial ELISA kits
- Secondary Outcome Measures
Name Time Method changes in blood zinc levels baseline to 12 weeks Zinc levels in blood will be analyzed in trace element- free tubes and assayed by atomic absorption spectrophotometry using standard reference material obtained from the National Institute of Standards and Technology to check the accuracy and precision of the determinations
changes in upper respiratory infection questionnaire score baseline to 28 weeks Upper respiratory tract infections will be tracked using the Jackson and Dowling questionnaire. The questionnaire will be completed daily by participants, either manually or electronically , throughout the 28-week study period. The scale for the questionnaire is from 0-42. The higher score means worse outcome.
changes in blood vitamin E levels baseline to 28 weeks Vitamin E levels in the blood will be extracted with hexane, dried and assayed for alpha and gamma tocopherol by high pressure liquid chromatography (HPLC) using a normal-phase diol column and florescence detection according to the method of Kramer and colleagues (2005).
Trial Locations
- Locations (1)
Loma Linda University School of Public Health
🇺🇸Loma Linda, California, United States