Literature DB >> 31206659

MAIT cells as attractive vaccine targets.

A Michael Downey1, Paulina Kapłonek1,2, Peter H Seeberger1,2.   

Abstract

Mucosal-associated invariant T (MAIT) cells are a subset of T cells that perform innate-like immunity functions upon recognition of small molecule vitamin B metabolites presented by the MHC, class I-related protein-1 (MR1). MAIT cells are profuse in humans, but especially abundant in blood, liver, lungs, and mucosal layers. The mucosa is a common site of carcinogenesis and MAIT cells have been found in both primary and metastatic tumors. MAIT cells target a host of microbes including Mycobacterium tuberculosis, Staphylococcus aureus, Salmonella enterica, Legionella longbeachae, Escherichia coli, and Candida albicans, and are highly activated in viral infections. Cytokines produced by MAIT cells are both anticancerous and antibacterial, but also have proinflammatory and possibly tumorigenic properties. In addition, it is believed that MAIT cells play a protective role in viral infections in an MR1-independent fashion. Based on our summary of recent advances concerning both MR1-mediated and MR1-independent MAIT cell immune responses, we weigh the strengths and weaknesses of these cells for vaccine development.
© 2019 Federation of European Biochemical Societies.

Entities:  

Keywords:  MAIT cells; antitumorigenic; antiviral; bacterial infection; immunomodulation; therapeutics; vaccines

Mesh:

Substances:

Year:  2019        PMID: 31206659     DOI: 10.1002/1873-3468.13488

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  9 in total

1.  Efficient 5-OP-RU-Induced Enrichment of Mucosa-Associated Invariant T Cells in the Murine Lung Does Not Enhance Control of Aerosol Mycobacterium tuberculosis Infection.

Authors:  Charles Kyriakos Vorkas; Olivier Levy; Miroslav Skular; Kelin Li; Jeffrey Aubé; Michael S Glickman
Journal:  Infect Immun       Date:  2020-12-15       Impact factor: 3.441

2.  Chemical Modulators of Mucosal Associated Invariant T Cells.

Authors:  Jeffrey Y W Mak; Ligong Liu; David P Fairlie
Journal:  Acc Chem Res       Date:  2021-08-20       Impact factor: 22.384

Review 3.  Development of a vaccine against Staphylococcus aureus invasive infections: Evidence based on human immunity, genetics and bacterial evasion mechanisms.

Authors:  Lloyd S Miller; Vance G Fowler; Sanjay K Shukla; Warren E Rose; Richard A Proctor
Journal:  FEMS Microbiol Rev       Date:  2020-01-01       Impact factor: 16.408

4.  Augmentation of the Riboflavin-Biosynthetic Pathway Enhances Mucosa-Associated Invariant T (MAIT) Cell Activation and Diminishes Mycobacterium tuberculosis Virulence.

Authors:  Ruchi Jain Dey; Bappaditya Dey; Melanie Harriff; Elizabeth T Canfield; David M Lewinsohn; William R Bishai
Journal:  mBio       Date:  2022-02-15       Impact factor: 7.867

Review 5.  Mouse models illuminate MAIT cell biology.

Authors:  Huimeng Wang; Zhenjun Chen; James McCluskey; Alexandra J Corbett
Journal:  Mol Immunol       Date:  2020-12-22       Impact factor: 4.407

Review 6.  MAIT Cell Activation and Functions.

Authors:  Timothy S C Hinks; Xia-Wei Zhang
Journal:  Front Immunol       Date:  2020-05-27       Impact factor: 7.561

Review 7.  Antigen Recognition by MR1-Reactive T Cells; MAIT Cells, Metabolites, and Remaining Mysteries.

Authors:  Alexandra J Corbett; Wael Awad; Huimeng Wang; Zhenjun Chen
Journal:  Front Immunol       Date:  2020-08-27       Impact factor: 7.561

Review 8.  Vaccination Against Tuberculosis: Revamping BCG by Molecular Genetics Guided by Immunology.

Authors:  Stefan H E Kaufmann
Journal:  Front Immunol       Date:  2020-02-27       Impact factor: 7.561

9.  Human MAIT Cells Respond to Staphylococcus aureus with Enhanced Anti-Bacterial Activity.

Authors:  Andrew J R Cooper; Jonah Clegg; Féaron C Cassidy; Andrew E Hogan; Rachel M McLoughlin
Journal:  Microorganisms       Date:  2022-01-12
  9 in total

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