Synthetic 5-amino-6-Dribitylaminouracil paired with inflammatory stimuli facilitates MAIT cell expansion in vivo.

Nelson, Adam G.; Huimeng Wang; Dewar, Phoebe M.; Eddy, Eleanor M.; Songyi Li; Xin Yi Lim; Patton, Timothy; Yuchen Zhou; 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.; Zhenjun Chen

Introduction: Mucosal-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. Methods: Here,we outline threemethods to increase the abundance of MAIT cells in C57BL/6 mice using a combination of inflammatory stimuli, 5-A-RU and MG. Results: Our 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. Conclusion: These 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.

MICROBIOLOGICAL synthesis; LABORATORY mice; T cells; CELL populations; ANIMAL disease models

Frontiers in Immunology, 2023, p1

1664-3224

Academic Journal

10.3389/fimmu.2023.1109759