| Literature DB >> 31763782 |
Zhenjun Chen1, Huimeng Wang1, Criselle D'Souza2, Hui-Fern Koay1, Bronwyn Meehan1, Zhe Zhao1, Troi Pediongco1, Mai Shi1,3, Tianyuan Zhu1, Bingjie Wang1, Lars Kjer-Nielsen1, Sidonia B G Eckle1, Jamie Rossjohn4,5,6, David P Fairlie7,8, Dale I Godfrey1,9, Richard A Strugnell1, James McCluskey1, Alexandra J Corbett1.
Abstract
This unit describes the utility of various mouse models of infection and immunization for studying mucosal-associated invariant T (MAIT) cell immunity: MAIT cells can be isolated from the lungs (or from other tissues/organs) and then identified and characterized by flow cytometry using MR1 tetramers in combination with a range of antibodies. The response kinetics, cytokine profiles, and functional differentiation of lung MAIT cells are studied following infection with the bacterial pathogen Legionella longbeachae or Salmonella enterica Typhimurium or immunization with synthetic MAIT cell antigen plus Toll-like receptor agonist. MAIT cells enriched or expanded during the process can be used for further studies. A step-by-step protocol is provided for MAIT cell sorting and adoptive transfer. Mice can then be challenged and MAIT cells tracked and further examined.Entities:
Keywords: MR1 tetramers; flow cytometry; mouse models; mucosal-associated invariant T (MAIT) cells; respiratory infection
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Year: 2019 PMID: 31763782 DOI: 10.1002/cpim.89
Source DB: PubMed Journal: Curr Protoc Immunol ISSN: 1934-3671