Function and regulation of mucosal associated invariant T cells in the lung

NIH RePORTER · NIH · R01 · $519,683 · view on reporter.nih.gov ↗

Abstract

Project Summary/Abstract Asthma remains a serious public health threat with unmet therapeutic needs. The development of successful therapies relies a more in-depth understanding of the immune subsets and pathways involved. MAIT cells are innate-like T cells that recognize microbial riboflavin metabolites presented by MR1 and can function through both TCR dependent and independent pathways. Interestingly, previous studies indicated an inverse association between MAIT cells and human asthma. The precise role of MAIT cells in asthma development and exacerbation, however, remains unknown. We hypothesize that a deficiency of MAIT cells in asthma patients contributes to exacerbated airway inflammatory responses to allergen and other stimulus, and that increasing MAIT cell numbers may help prevent asthma development and exacerbation. Using fresh lung samples from deceased organ donors, we will examine the abundance, heterogeneity and function of lung-resident MAIT cells in severe asthma patients and control individuals without lung diseases. We will use MAIT cell deficient mice and adoptive transfer strategies to interrogate the specific roles of MAIT cells in allergen and air pollutant- induced airway inflammation. Finally, we will test whether boosting the number of MAIT cells by an engineered probiotic strain can help prevent severe asthma development and exacerbation.

Key facts

NIH application ID
10531769
Project number
7R01HL155021-02
Recipient
RBHS-ROBERT WOOD JOHNSON MEDICAL SCHOOL
Principal Investigator
Qi yang
Activity code
R01
Funding institute
NIH
Fiscal year
2021
Award amount
$519,683
Award type
7
Project period
2021-11-24 → 2026-06-30