Impact of High Dietary Fiber on Microbiome and Vaccine Responses

M.D. Anderson Cancer Center

Status: Active, not recruiting

Conditions: Influenza

Treatments: Dietary Supplement: Prebiotic Food-Enriched Diet (PreFED); Dietary Supplement: High-Fiber Diet (HFD)

Study type: Interventional

Funder types: Other

Identifiers

NCT05565586

2022-0450

NCI-2022-07926 (Other Identifier)

Details and patient eligibility

About

To learn if diet can enhance the microbes (such as bacteria and viruses) found in your gut and improve the body's immune response to the influenza (flu) vaccine.

Full description

Primary Objectives:

--To determine the feasibility of two dietary intervention strategies focused on fiber-rich and prebiotic foods prior to seasonal influenza vaccination. Feasibility is defined as ≥ 80% of subjects being compliant with the intervention.

Secondary Objectives:

• To evaluate the effects of each dietary intervention on the composition, diversity and function of the gut microbiome.
• To assess the effects of each dietary intervention on response to influenza vaccination as measured by vaccine-specific immune response.
• To assess the effects of each dietary intervention on systemic immunity.

Exploratory Objectives:

• To interrogate the overlap between the identified gut microbial and dietary patterns associated with vaccine response and those associated with excellent or poor responses to cancer immunotherapy (from our own published work and internal cohorts).
• To identify components and determinants of the gut microbiome that could be modulated to enhance vaccine response.
• To determine how modulation of the gut microbiome can be achieved through fiber and prebiotic-focused dietary changes.

Enrollment: 31 patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

1. MD Anderson employees with existing MRNs
2. Body Mass Index (BMI) 18.5-40 kg/m2
3. Age 18 or older
4. Intends to receive the seasonal influenza vaccine at MD Anderson through Employee Health (starting Fall of 2022)
5. Willing to adhere to the provided dietary interventions
6. Willing to provide blood and stool specimens, complete diet questionnaires and logs, and pick up food on-site within the study schedule
7. English-speaking
8. Has easy access to a scale at home, work, or in their community

Exclusion criteria

1. Contraindication to the recommended annual influenza vaccine
2. Medical contraindications to the intervention diet
3. Major dietary restrictions (including vegetarian or vegan diets) or food allergies
4. Unable or unwilling to undergo study procedures
5. Has diabetes mellitus requiring medical treatment
6. Has inflammatory bowel disease
7. Has a history of bariatric surgery
8. Has a history of major gastrointestinal surgery (not including appendectomy or cholecystectomy)
9. Antibiotic use within 30 days of study initiation or planned antibiotic treatment during study course
10. Habitual consumption of a high fiber diet
11. Use of a supplement containing fiber/prebiotics/probiotics within 30 days of study initiation
12. Women who are pregnant, planning to become pregnant, or who are lactating may not be included in this study

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Single Group Assignment

Masking: None (Open label)

---

31 participants in 2 patient groups

High-Fiber Diet (HFD) Intervention

Experimental group

Description:

Participants are expected to eat only the study meals and snacks provided

Treatment:

Dietary Supplement: High-Fiber Diet (HFD)

Prebiotic Food-Enriched Diet (PreFED) Intervention

Experimental group

Description:

Participants are expected to incorporate study snacks and meal components provided into your usual diet.

Treatment:

Dietary Supplement: Prebiotic Food-Enriched Diet (PreFED)