# Mucosal-associated invariant T (MAIT) cell responses in Salmonella enterica serovar Typhi strain Ty21a oral vaccine recipients

## TL;DR

This study shows how MAIT cells respond to a typhoid vaccine, suggesting their role in protecting against bacterial infections in the gut.

## Contribution

The study reveals that MAIT cells are modulated after Ty21a vaccination, highlighting their potential in mucosal immunity.

## Key findings

- Circulating MAIT cells decreased in frequency but showed increased activation after vaccination.
- MAIT cells exhibited higher gut-homing markers, indicating potential migration to mucosal sites.
- TNF expression by MAIT cells was elevated post-vaccination, while other functions remained unchanged.

## Abstract

Mucosal–associated invariant T (MAIT) cells are unconventional innate-like T cells abundant in human mucosal tissues and are associated with protective responses to microbial infections. MAIT cells have the capacity for rapid effector functions, including the secretion of cytokines and cytotoxic molecules. In this study, we examined the longitudinal circulating MAIT cell response to the live attenuated oral vaccine Ty21a (Ty21a) against Salmonella enterica serovar Typhi (S. Typhi). We enrolled healthy adults who received a course of oral live-attenuated S. Typhi strain Ty21a vaccine and assessed peripheral blood MAIT cell longitudinal responses pre-vaccination, and at seven days and one-month post-vaccination, using flow cytometry, cell migration, and tetramer decay assays. We showed that following vaccination, circulating MAIT cells were lower in frequency, but were more activated, and had higher levels of gut-homing marker integrin α4β7 and chemokine receptors CCR9 and CCR6, suggesting the potential of MAIT cells to migrate to mucosal sites. We found no significant differences in MAIT cell functionality, cytotoxicity and T-cell receptor avidity, except in TNF expression, which was higher post-vaccination. We show that MAIT cell immune responses are modulated post-vaccination against S. Typhi. This study contributes to our understanding of MAIT cells’ potential role in oral vaccination against bacterial mucosal pathogens.