Author:
Nelson Adam G.,Wang Huimeng,Dewar Phoebe M.,Eddy Eleanor M.,Li Songyi,Lim Xin Yi,Patton Timothy,Zhou Yuchen,Pediongco Troi J.,Meehan Lucy J.,Meehan Bronwyn S.,Mak Jeffrey Y. W.,Fairlie David P.,Stent Andrew W.,Kjer-Nielsen Lars,McCluskey James,Eckle Sidonia B. G.,Corbett Alexandra J.,Souter Michael N. T.,Chen Zhenjun
Abstract
IntroductionMucosal-associated invariant T (MAIT) cells are a population of innate-like T cells, which mediate host immunity to microbial infection by recognizing metabolite antigens derived from microbial riboflavin synthesis presented by the MHC-I-related protein 1 (MR1). Namely, the potent MAIT cell antigens, 5-(2-oxopropylideneamino)-6-D-ribitylaminouracil (5-OP-RU) and 5-(2-oxoethylideneamino)-6-D-ribitylaminouracil (5-OE-RU), form via the condensation of the riboflavin precursor 5-amino-6-D-ribitylaminouracil (5-A-RU) with the reactive carbonyl species (RCS) methylglyoxal (MG) and glyoxal (G), respectively. Although MAIT cells are abundant in humans, they are rare in mice, and increasing their abundance using expansion protocols with antigen and adjuvant has been shown to facilitate their study in mouse models of infection and disease. MethodsHere, we outline three methods to increase the abundance of MAIT cells in C57BL/6 mice using a combination of inflammatory stimuli, 5-A-RU and MG.ResultsOur data demonstrate that the administration of synthetic 5-A-RU in combination with one of three different inflammatory stimuli is sufficient to increase the frequency and absolute numbers of MAIT cells in C57BL/6 mice. The resultant boosted MAIT cells are functional and can provide protection against a lethal infection of Legionella longbeachae.ConclusionThese results provide alternative methods for expanding MAIT cells with high doses of commercially available 5-A-RU (± MG) in the presence of various danger signals.
Subject
Immunology,Immunology and Allergy
Cited by
1 articles.
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