Determining the Relationship Between Gut Microbiota and Immune Response to Influenza or COVID-19 Vaccine
NCT ID: NCT05584735
Last Updated: 2025-07-31
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
46 participants
OBSERVATIONAL
2023-11-03
2025-03-20
Brief Summary
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Detailed Description
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It is known that patients with IBD have dysbiosis of their gut microbiome and those immunosuppressed may have a lower vaccine response. In this aim, the investigators will evaluate whether differences in microbial diversity predict immune response to the influenza and COVID-19 vaccine.
In this prospective study, immunosuppressed IBD patients will be vaccinated per standard of care and blood will be collected to measure the immune response. A fecal and saliva sample will be collected to characterize the gut microbiome. The investigators hypothesize that reduced richness / alpha-diversity in gut microbiota will correlate with those with a blunted vaccine response.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Participants with Inflammatory Bowel Disease (IBD)
Participants with IBD who are receiving a flu or COVID-19 vaccine
Influenza vaccine
Observe effects of flu vaccine on microbiome
COVID-19 vaccine
Observe effects of COVID-19 vaccine on microbiome
Interventions
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Influenza vaccine
Observe effects of flu vaccine on microbiome
COVID-19 vaccine
Observe effects of COVID-19 vaccine on microbiome
Eligibility Criteria
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Inclusion Criteria
* Currently one of the following groups:
1. Group A: Anti-TNF Therapy Group
* Maintenance monotherapy: infliximab (at least every 8 weeks), golimumab (at least monthly), adalimumab (at least every 2 weeks), or certolizumab (at least monthly)
* Combination Therapy: Anti-TNF Combination Therapy Group on anti-TNF therapy as described above along with either methotrexate, azathioprine, or 6MP
2. Group B: Non-TNG biologic
* Ustekinumab Therapy: on either ustekinumab monotherapy or combination therapy with methotrexate, azathioprine, or 6MP
* Vedolizumab Therapy: on either vedolizumab monotherapy or combination therapy with methotrexate, azathioprine, or 6MP
* Risankizumab Therapy: 360mg at least every 8 weeks
3. Group C: Janus Kinase Therapy
* Tofacitinib Therapy: at least 5mg PO BID
* Upadactinib Therapy: at least 15mg PO daily
* Patient has been on stable treatment for IBD for at least three months
* Must be able to provide research samples between 28-65 days post influenza or Covid-19 vaccination.
Exclusion Criteria
* Recent oral antibiotics within previous 2 months
18 Years
64 Years
ALL
No
Sponsors
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University of Wisconsin, Madison
OTHER
Responsible Party
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Principal Investigators
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Freddy Caldera, DO, MS
Role: PRINCIPAL_INVESTIGATOR
University of Wisconsin, Madison
Locations
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University of Wisconsin School of Medicine and Public Health
Madison, Wisconsin, United States
Countries
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Other Identifiers
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A534250
Identifier Type: OTHER
Identifier Source: secondary_id
SMPH/MEDICINE/GASTROENT
Identifier Type: OTHER
Identifier Source: secondary_id
Protocol version 7/18/2024
Identifier Type: OTHER
Identifier Source: secondary_id
2021-0977
Identifier Type: -
Identifier Source: org_study_id
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