Probiotics may supercharge COVID-19 shots, study finds
NCT ID NCT07610512
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether taking daily probiotic capsules for 4-5 weeks after a COVID-19 vaccine could improve the body's immune response. 138 healthy adults received either probiotics or a placebo. Researchers measured antibody levels and T-cell activity to see if probiotics made the vaccine work better or reduced side effects.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Probiotics (Lactobacillus spp.)
- What this could lead to
- If probiotics enhance vaccine immunity, this could point toward a simple way to improve vaccine effectiveness.
- What could go wrong
- This is a small, completed study with no results posted yet. Probiotics may not meaningfully change immune responses, and effects may vary by individual.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
138 people
The number who actually took part.
- Started
-
Oct 2021
- Finished
-
Mar 2022
- Lead sponsor
-
A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
20 to 65 years
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Male or female subject ≥ 20 to ≤ 65 years of age at the time signing informed consent form. 2. Body weight ≥50 kgs 3. Must be scheduling to receive a BNT162b2 mRNA COVID-19 vaccine 4. Being able to comply with the study protocol 5. Being able to independently provide written informed consent Exclusion Criteria: 1. Taking antibiotic at enrollment 2. Taking immunomodulatory (e.g., steroid) or anti-histamine drugs 3. Took pre- or probiotics within the past 30 days 4. Being to expected to take other probiotic supplement during the study period 5. Being expected to take antibiotic during the study period 6. A history of hypersensitivity or severe allergic reaction to any components of the probiotics or placebo supplement 7. Pregnant or breastfeeding 8. Having a severe immunocompromised disorder (e.g. HIV infection) 9. Solid organ or bone marrow transplant recipients 10. Major gastrointestinal surgery within 3 months before enrollment 11. Having severe active gastrointestinal conditions, including inflammatory bowel disease or diverticulitis 12. No self-reported symptoms of an upper airway infection with the past 2 weeks 13. A history of SARS-CoV-2 infection 14. Previously participated in investigational study involving SARS-CoV-2 vaccines or therapies
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Taipei Medical University Hospital.
Taipei, Taiwan
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Other studies related to the condition(s) this trial covers.
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