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Dietary Inulin to Improve SARS-CoV-2 Vaccine Response in Kidney Transplant Recipients: The RIVASTIM-Inulin Randomised Controlled Trial.

Authors :
Singer, Julian
Tunbridge, Matthew J.
Shi, Bree
Perkins, Griffith B.
Chai, Cheng Sheng
Salehi, Tania
Sim, Beatrice Z.
Kireta, Svjetlana
Johnston, Julie K.
Akerman, Anouschka
Milogiannakis, Vanessa
Aggarwal, Anupriya
Turville, Stuart
Hissaria, Pravin
Ying, Tracey
Wu, Huiling
Grubor-Bauk, Branka
Coates, P. Toby
Chadban, Steven J.
Source :
Vaccines; Jun2024, Vol. 12 Issue 6, p608, 20p
Publication Year :
2024

Abstract

Kidney transplant recipients are at an increased risk of hospitalisation and death from SARS-CoV-2 infection, and standard two-dose vaccination schedules are typically inadequate to generate protective immunity. Gut dysbiosis, which is common among kidney transplant recipients and known to effect systemic immunity, may be a contributing factor to a lack of vaccine immunogenicity in this at-risk cohort. The gut microbiota modulates vaccine responses, with the production of immunomodulatory short-chain fatty acids by bacteria such as Bifidobacterium associated with heightened vaccine responses in both observational and experimental studies. As SCFA-producing populations in the gut microbiota are enhanced by diets rich in non-digestible fibre, dietary supplementation with prebiotic fibre emerges as a potential adjuvant strategy to correct dysbiosis and improve vaccine-induced immunity. In a randomised, double-bind, placebo-controlled trial of 72 kidney transplant recipients, we found dietary supplementation with prebiotic inulin for 4 weeks before and after a third SARS-CoV2 mRNA vaccine to be feasible, tolerable, and safe. Inulin supplementation resulted in an increase in gut Bifidobacterium, as determined by 16S RNA sequencing, but did not increase in vitro neutralisation of live SARS-CoV-2 virus at 4 weeks following a third vaccination. Dietary fibre supplementation is a feasible strategy with the potential to enhance vaccine-induced immunity and warrants further investigation. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
2076393X
Volume :
12
Issue :
6
Database :
Complementary Index
Journal :
Vaccines
Publication Type :
Academic Journal
Accession number :
178194426
Full Text :
https://doi.org/10.3390/vaccines12060608