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MAIT cells derived ligands signal via VEGFR2 to promote tissue repair and liver regeneration

Sayaf, K.; Lett, M.; Powell, K.; Tasin, I.; Garner, L.; Bhandari, A.; Ramamurthy, N.; Russo, F. P.; Klenerman, P.; Hackstein, C.-P.

2026-03-25 immunology
10.64898/2026.03.23.713159 bioRxiv
Show abstract

MAIT are a highly versatile population of innate-like T cells that have been implicated in promoting tissue repair-associated process in a variety of tissue and diseases settings in the last years. While certain specific effector molecules responsible for MAIT-cell mediated have been identified, the mechanisms by which MAIT cells exert repair functions remain incompletely understood. Here, we show that hepatic MAIT cells express VEGFA, VEGFB and vimentin, an alternative ligand for the VEGFA-receptor VEGFR2 in both, regenerating and heathy tissue. Expression and secretion of these factors were induced in vitro by combined T cell receptor and cytokine stimulation. Supernatants of activated MAIT cells were able to promote proliferation of different epithelial and endothelial cells, including a liver sinusoidal endothelial-derived cell line in an VEGFR2-dependent manner. Together, our findings expand our understanding of MAIT cell function, especially in the liver and open new opens avenues for exploring MAIT therapeutic potential in modulating tissue repair.

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