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Immuno-Microbial Signature of Vaccine-Induced Immunity against SARS-CoV-2
Lesley Umeda1, Amada Torres2, Braden P Kunihiro1
1Department of Molecular Biosciences and Bioengineering, University of Hawaii, Honolulu, HI 96822, USA.
Vaccines
|June 27, 2024
Summary
Pre-vaccination gut microbiome and inflammation, particularly high mobility group box 1 (HMGB-1) levels, can predict SARS-CoV-2 mRNA vaccine effectiveness in generating neutralizing antibodies.
Area of Science:
- Immunology
- Microbiome Research
- Vaccinology
Background:
- Individual responses to vaccines vary significantly, impacting public health outcomes.
- Understanding these differences is crucial for optimizing vaccine effectiveness and disease control strategies.
Purpose of the Study:
- To investigate inter-individual differences in SARS-CoV-2 mRNA vaccine responses.
- To examine the relationship between pre-vaccination immunological and gut microbiota features and post-vaccination neutralizing antibody levels.
Main Methods:
- Pilot study involving 14 adults, collecting blood and stool samples pre- and post-vaccination.
- Post-hoc grouping into high (HN) and low (LN) neutralizing antibody responders at 10 weeks.
- Bivariate correlation analysis to assess associations between gut microbiota, inflammation, and neutralization capacity.
Main Results:
- Significant pre-vaccination differences in gut microbiome composition and inflammation distinguished future vaccine responders.
- Higher abundance of Prevotella in the LN group, negatively correlated with IL-17 but positively with HMGB-1.
- A significant inverse correlation was found between pre-vaccination HMGB-1 levels and neutralization capacity at 10 weeks.
Conclusions:
- Pre-vaccination gut microbial signatures and inflammation, specifically HMGB-1, may serve as predictive biomarkers for SARS-CoV-2 mRNA vaccine effectiveness.
- These findings highlight the potential of targeting the gut microbiome to enhance vaccine-induced immunity.
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