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  MAIT cells as attractive vaccine targets

Downey, M., Kapłonek, P., & Seeberger, P. H. (2019). MAIT cells as attractive vaccine targets. FEBS Letters, 593, 1627-1640. doi:10.1002/1873-3468.13488.

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Item Permalink: http://hdl.handle.net/21.11116/0000-0003-E757-7 Version Permalink: http://hdl.handle.net/21.11116/0000-0004-5D6D-B
Genre: Journal Article

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 Creators:
Downey, Michael1, Author              
Kapłonek, Paulina1, Author              
Seeberger, Peter H.2, Author              
Affiliations:
1Peter H. Seeberger - Vaccine Development, Biomolekulare Systeme, Max Planck Institute of Colloids and Interfaces, Max Planck Society, ou_1863308              
2Peter H. Seeberger, Biomolekulare Systeme, Max Planck Institute of Colloids and Interfaces, Max Planck Society, ou_2040285              

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Free keywords: MAIT cells, vaccines, therapeutics, immunomodulation, bacterial infection, antiviral, anti-tumorigenic
 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 Accepted Article This article is protected by copyright. All rights reserved. in an MR1-independent fashion. Based on our summary of recent advances concerning both MR1-mediated and MR1-independent MAIT cell immune responses,

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Language(s): eng - English
 Dates: 2019-06-052019-06-272019
 Publication Status: Published in print
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 Identifiers: DOI: 10.1002/1873-3468.13488
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Title: FEBS Letters
  Other : FEBS Lett.
Source Genre: Journal
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Publ. Info: Chichester : Wiley
Pages: - Volume / Issue: 593 Sequence Number: - Start / End Page: 1627 - 1640 Identifier: ISSN: 0014-5793
ISSN: 1873-3468 (online)