Snack Foods and Their Impact on the Immune Response Following Influenza Vaccination

Immune Response Clinical Trial

— NutrImmune  

Official title:

Snack Foods and Their Impact on Immune Optimisation to the Influenza Vaccination: a Randomised Controlled Trial of a Vaccination Model of Immune Response

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05515263
• Other study ID #: HR/DP-21/22-33040
• Status: Recruiting
• Phase: N/A
• Start date: September 9, 2022
• Est. completion date: June 2024

Study information

• Verified date: July 2023
• Source: King's College London
• Contact: Alice van der Schoot, MSc
• Phone: 020 7848 4552
• Email: nutrimmune[@]kcl.ac.uk
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the impact of replacing usual snacks with alternative snack foods on the immune response to influenza vaccination in a population of healthy, middle-aged adults.

Description:

Nutrition plays an important role in the immune system by providing energy and metabolites to support the function of immune cells, allowing them to initiate effective immune responses. Diet is therefore a modifiable factor in impacting immune function and is currently a topic of substantial interest in health research. Snack consumption has been shown to account for approximately 20-30% of daily energy intake in adults. Therefore, snack choices have the potential to influence dietary intake and quality, and therefore immune function, both positively and negatively. This study assesses the effect of replacing usual snacks with alternative snack foods on the immune response in a model of viral infection - the seasonal influenza vaccine containing four prevalent influenza virus strains for the 2022/23 or 2023/24 influenza season, as determined by the World Health Organization.

This study is a parallel group, randomised controlled trial that will examine the replacement of usual snack foods with alternative snack foods on the immune response to seasonal influenza vaccination in humans, which will be assessed by measuring rates of seroconversion, and other immunological markers following vaccination. The intervention will be for 8 weeks, and influenza vaccination will be administered at 4-week midpoint. Participants will be followed up 3 months post-vaccination to assess incidence of upper respiratory symptoms.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 88
• Est. completion date: June 2024
• Est. primary completion date: June 2024
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 40 Years to 64 Years

Eligibility

Inclusion Criteria:

1. Men or women, aged between 40-64 years

2. Body mass index (BMI) of 18.50 - 29.99 kg/m2

3. Individuals who regularly consume snacks (=2 per day, excluding fruit, vegetable, nut and seed snacks)

4. Fibre intake <30 g/d

5. Willing to avoid receiving any vaccination (except for COVID-19 vaccination) from one month prior to the baseline visit until completion of the 8-week intervention period

6. Willing to avoid receiving any COVID-19 vaccination/booster between week 2 and week 8 of the intervention period

7. Willing to discontinue use of prebiotics and probiotics during the trial

8. Willing to follow the protocol and provide consent

Exclusion Criteria:

1. Allergy or intolerance to any intervention products

2. Dislike of any intervention products

3. Immunodeficiency/immunosuppression due to disease or medication, such as:

• Chronic inflammatory disease or autoimmune disease (e.g., rheumatoid arthritis, inflammatory bowel disease, psoriasis) or primary or secondary immunodeficiency disease (e.g., HIV infection)

• Ongoing therapy with immunomodulators or immunosuppressants (e.g., chemotherapy, oral corticosteroids, daily use of inhaled or nasal corticosteroids)

• Other immunodeficient state (e.g., asplenia).

4. Medical history of any of the following: diabetes, major active psychiatric conditions (e.g. schizophrenia), current eating disorder, alcohol abuse, active treatment for cancer in the last year, severe neurological, endocrine, renal, cardiac or pulmonary disease (or any other chronic medical condition), severe oesophagitis, gastritis or duodenitis, active diverticulitis or intestinal/colonic strictures, Coeliac disease, Crohn's disease or Ulcerative colitis, stem cell or organ transplant, gut resection surgery, bleeding disorder, anaphylaxis or any other major or chronic condition known to impact study outcome measures.

5. Ongoing use of antiviral agents, or any other drugs known to impact study outcome measures

6. Use of immunoglobulins and/or any blood products within the three months prior to vaccination

7. Ongoing use of anticoagulants (e.g., warfarin)

8. Antibiotic treatment in the month prior to the start of the study

9. Consumption of probiotics or prebiotic products within the four weeks prior to the start of the study

10. History of severe adverse reaction and/or allergic reaction associated with the influenza vaccine or any other vaccine

11. Known allergy or hypersensitivity to any component of the vaccine including: sodium chloride, potassium chloride, magnesium chloride hexahydrate, disodium phosphate dihydrate, potassium dihydrogen phosphate; and possible trace residues: beta-propiolactone, cetyltrimethylammonium bromide, and polysorbate 80

12. Suffered from influenza illness in the six months prior to the start of the study

13. For participants recruited on or before 30/06/2023, exclusion criteria is: already vaccinated with any influenza vaccine licensed for the 2022/2023 season; For participants recruited after 30/06/2023, exclusion criteria is: already vaccinated with any influenza vaccine licensed for the 2023/2024 season

14. Received any influenza vaccination within six months prior to the start of the study

15. Received any other vaccinations within one month prior to the start of the study (except for COVID-19 vaccination)

16. Women who are pregnant, lactating or planning pregnancy

17. Ongoing alcohol, drug or medication abuse

18. Unexplained or unintentional weight loss in the past six months

Related Conditions & MeSH terms

• Immune Response

Intervention

Dietary Supplement:
• Intervention snack
To be eaten in replacement of usual snacks twice a day for 8 weeks.
• Control snack
To be eaten in replacement of usual snacks twice a day for 8 weeks.

Locations

Country	Name	City	State
United Kingdom	King's College London	London

Sponsors (1)

Lead Sponsor	Collaborator
King's College London

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Rates of seroconversion for =1 influenza virus strain	The proportion of participants achieving seroconversion (=4-fold increase in specific antibody titre) in at least one influenza virus strain. Titres will be assessed using the Hemagglutination Inhibition Assay (HAI) and fold change will be calculated.	Week 8
Secondary	Rates of seroconversion for A/Wisconsin/588/2019 (H1N1)pdm09-like virus strain (strain 1a)	The proportion of participants achieving seroconversion for A/Wisconsin/588/2019 (H1N1)pdm09-like virus strain. Titres will be assessed by HAI and fold change will be calculated.	Week 8
Secondary	Rates of seroconversion for A/Wisconsin/67/2022 (H1N1)pdm09-like virus strain (strain 1b)	The proportion of participants achieving seroconversion for A A/Wisconsin/67/2022 (H1N1)pdm09-like virus strain. Titres will be assessed by HAI and fold change will be calculated.	Week 8
Secondary	Rates of seroconversion for A/Darwin/6/2021 (H3N2)-like virus strain (strain 2)	The proportion of participants achieving seroconversion for A/Darwin/6/2021 (H3N2)-like virus strain. Titres will be assessed by HAI and fold change will be calculated.	Week 8
Secondary	Rates of seroconversion for influenza virus B/Austria/1359417/2021 (B/Victoria lineage)-like virus strain (strain 3)	The proportion of participants achieving seroconversion for B/Austria/1359417/2021 (B/Victoria lineage)-like virus strain. Titres will be assessed by HAI and fold change will be calculated.	Week 8
Secondary	Rates of seroconversion for B/Phuket/3073/2013 (B/Yamagata lineage)-like virus strain (strain 4)	The proportion of participants achieving seroconversion for B/Phuket/3073/2013 (B/Yamagata lineage)-like virus strain. Titres will be assessed by HAI and fold change will be calculated.	Week 8
Secondary	Proportion of participants who do not achieve seroconversion for any influenza virus strain	Titres will be assessed by HAI and fold change will be calculated.	Week 8
Secondary	Rates of seroconversion for only 1 influenza virus strain	The proportion of participants achieving seroconversion for 1 influenza virus strain. Titres will be assessed by HAI and fold change will be calculated.	Week 8
Secondary	Rates of seroconversion for 2 influenza virus strains	The proportion of participants achieving seroconversion for 2 influenza virus strains. Titres will be assessed by HAI and fold change will be calculated.	Week 8
Secondary	Rates of seroconversion for 3 influenza virus strains	The proportion of participants achieving seroconversion for 3 influenza virus strains. Titres will be assessed by HAI and fold change will be calculated.	Week 8
Secondary	Rates of seroconversion for 4 influenza virus strains	The proportion of participants achieving seroconversion for all 4 influenza virus strains. Titres will be assessed by HAI and fold change will be calculated.	Week 8
Secondary	Geometric mean antigen-specific titres for or A/Wisconsin/588/2019 (H1N1)pdm09-like virus strain (strain 1a)	Titres will be assessed by HAI.	Week 0, 4 and 8
Secondary	Geometric mean antigen-specific titres for A/Wisconsin/67/2022 (H1N1)pdm09-like virus strain (strain 1b)	Titres will be assessed by HAI.	Week 0, 4 and 8
Secondary	Geometric mean antigen-specific titres for A/Darwin/6/2021 (H3N2)-like virus strain (strain 2)	Titres will be assessed by HAI.	Week 0, 4 and 8
Secondary	Geometric mean antigen-specific titres for B/Austria/1359417/2021 (B/Victoria lineage)-like virus strain (strain 3)	Titres will be assessed by HAI.	Week 0, 4 and 8
Secondary	Geometric mean antigen-specific titres for B/Phuket/3073/2013 (B/Yamagata lineage)-like virus strain (strain 4)	Titres will be assessed by HAI assay.	Week 0, 4 and 8
Secondary	Fold change in antigen-specific titres for A/Wisconsin/588/2019 (H1N1)pdm09-like virus strain (strain 1a)	Titres will be assessed by HAI and fold change will be calculated.	Week 8
Secondary	Fold change in antigen-specific titres for A/Wisconsin/67/2022 (H1N1)pdm09-like virus strain (strain 1b)	Titres will be assessed by HAI and fold change will be calculated.	Week 8
Secondary	Fold change in antigen-specific titres for A/Darwin/6/2021 (H3N2)-like virus strain (strain 2)	Titres will be assessed by HAI and fold change will be calculated.	Week 8
Secondary	Fold change in antigen-specific titres for B/Austria/1359417/2021 (B/Victoria lineage)-like virus strain (strain 3)	Titres will be assessed by HAI and fold change will be calculated.	Week 8
Secondary	Fold change in antigen-specific titres for B/Phuket/3073/2013 (B/Yamagata lineage)-like virus strain (strain 4)	Titres will be assessed by HAI and fold change will be calculated.	Week 8
Secondary	Seroprotection for =1 influenza virus strain	The proportion of participants achieving seroprotection (HAI titre of =1:40) in at least one of the four influenza virus strains.	Week 8
Secondary	Seroprotection for A/Wisconsin/588/2019 (H1N1)pdm09-like virus strain (strain 1a)	The proportion of participants achieving seroprotection (HAI titre of =1:40) for A/Wisconsin/588/2019 (H1N1)pdm09-like virus strain.	Week 8
Secondary	Seroprotection for A/Wisconsin/67/2022 (H1N1)pdm09-like virus strain (strain 1b)	The proportion of participants achieving seroprotection (HAI titre of =1:40) for A/Wisconsin/67/2022 (H1N1)pdm09-like virus strain.	Week 8
Secondary	Seroprotection for A/Darwin/6/2021 (H3N2)-like virus strain (strain 2)	The proportion of participants achieving seroprotection (HAI titre of =1:40) for A/Darwin/6/2021 (H3N2)-like virus strain.	Week 8
Secondary	Seroprotection for B/Austria/1359417/2021 (B/Victoria lineage)-like virus strain (strain 3)	The proportion of participants achieving seroprotection (HAI titre of =1:40) for B/Austria/1359417/2021 (B/Victoria lineage)-like virus strain.	Week 8
Secondary	Seroprotection for B/Phuket/3073/2013 (B/Yamagata lineage)-like virus strain (strain 4)	The proportion of participants achieving seroprotection (HAI titre of =1:40) for B/Phuket/3073/2013 (B/Yamagata lineage)-like virus strain.	Week 8
Secondary	Proportion of participants who do not achieve seroprotection for any influenza virus strains	Seroprotection is defined as HAI titre of =1:40	Week 8
Secondary	Seroprotection for 1 influenza virus strain	The proportion of participants achieving seroprotection (HAI titre of =1:40) for 1 influenza virus strain.	Week 8
Secondary	Seroprotection for 2 influenza virus strains	The proportion of participants achieving seroprotection (HAI titre of =1:40) for 2 influenza virus strains.	Week 8
Secondary	Seroprotection for 3 influenza virus strains	The proportion of participants achieving seroprotection (HAI titre of =1:40) for 3 influenza virus strains.	Week 8
Secondary	Seroprotection for 4 influenza virus strains	The proportion of participants achieving seroprotection (HAI titre of =1:40) for all 4 influenza virus strains.	Week 8
Secondary	Markers of immunological function	Isolation of peripheral blood mononuclear cells (PBMCs) to assess markers of immunological function.	Week 0, 4 and 8
Secondary	Incidence of upper respiratory symptoms	Measured using the Wisconsin Upper Respiratory Symptom Survey (WURSS-24).	Week 4, 8, 12 and 16
Secondary	Faecal gut microbiota (composition, alpha- and beta-diversity)	Measured by 16S community profiling (Illumina Miseq) of bacterial genomic DNA isolated from stool samples.	Week 0, 4 and 8
Secondary	Faecal short-chain fatty acids (SCFA)	Measured by gas liquid chromatography of stool samples.	Week 0, 4 and 8
Secondary	Faecal water	Determined from stool samples by oven-drying.	Week 0, 4 and 8
Secondary	Gut symptoms	Measured using the Gastrointestinal Symptom Rating Scale (GSRS) (7-day diary; questionnaire).	Week 0, 4 and 8
Secondary	Stool frequency	Measured using self-reported number bowel movements daily recorded in a 7-day diary.	Week 0, 4 and 8
Secondary	Stool consistency	Measured using the Bristol stool form scale (7-day dairy; questionnaire).	Week 0, 4 and 8
Secondary	Serum Vitamin E levels	Measured in blood sample - analysis of serum vitamin E levels by Liquid chromatography-mass spectrometry.	Week 0, 4 and 8
Secondary	Serum Zinc levels	Measured in blood sample - analysis of serum zinc levels by automated assay.	Week 0, 4 and 8
Secondary	Mental health status	Measured using The Patient Health Questionnaire Anxiety and Depression Scale (PHQ-ADS). Scores range from 0-48 with higher scores indicating more severe depression/anxiety.	Week 0, 4 and 8
Secondary	Dietary intake	7-day food and drink diary.	Week 0, 4 and 8
Secondary	Physical activity	Measured using the International Physical Activity Questionnaire (IPAQ).	Week 0, 4 and 8
Secondary	Acceptability of snack products	Measured using an Acceptability of dietary intervention questionnaire developed by King's College London for use in dietary intervention studies. The questionnaire assesses acceptability using a number of domains including flavour, texture, portion size.	Week 8
Secondary	Compliance	Return of unused snacks at the final visit (consumption of >75% of total snacks will be considered compliant).	Week 8
Secondary	Adverse events	Interview-administered questionnaire.	Week 0 - 8