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Induction of Intestinal Inflammation by Adoptive Transfer of CBir1 TCR Transgenic CD4+ T Cells to Immunodeficient Mice
Published on: December 16, 2021
B cells modulate mucosal associated invariant T cell immune responses
Rosangela Salerno-Goncalves1, Tasmia Rezwan1, Marcelo B Sztein1
1Department of Pediatrics, Center for Vaccine Development (CVD), University of Maryland School of Medicine , Baltimore, MD , USA.
Mucosal associated invariant T (MAIT) cells, activated by B cells infected with gut bacteria, may explain pre-existing immune responses to enteric vaccines. Bacterial load influences MAIT cell cytokine profiles.
Area of Science:
- Immunology
- Microbiology
- Vaccinology
Background:
- Pre-existing T cell immunity to enteric bacterial vaccines is common but poorly understood.
- Mucosal associated invariant T (MAIT) cells exhibit broad immune responses to various microbes, including enteric bacteria.
Purpose of the Study:
- To investigate if MAIT cell responses to intestinal bacteria contribute to pre-existing immunity observed before enteric vaccine administration.
- To explore the role of B cells in presenting antigens to MAIT cells in the context of gut microbiota surveillance.
Main Methods:
- Measurement of MAIT cell immune responses in healthy individuals without prior oral immunization.
- Assessment of MAIT cell activation by B cells infected with commensal and pathogenic enteric bacteria (Enterobacteriaceae family).
- Analysis of MR1 restriction, endocytic pathway involvement, and cytokine profiles in response to varying bacterial loads.
Main Results:
- MAIT cells were activated by B cells infected with diverse enteric bacteria but not by uninfected cells.
- MAIT cell activation was MR1-restricted and involved the endocytic pathway.
- Cytokine profiles of MAIT cell responses depended on bacterial load, suggesting a threshold for MR1 expression is necessary for activation.
Conclusions:
- B cells act as antigen-presenting cells for MAIT cells in response to enteric bacterial infections.
- MAIT cell responses are influenced by bacterial load and MR1 expression thresholds.
- These findings offer insights into gut immune surveillance and the nature of background immune responses to enteric bacteria.
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