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Am J Pathol ; 194(7): 1248-1261, 2024 Jul.
Article in English | MEDLINE | ID: mdl-38599461

ABSTRACT

Mucosal-associated invariant T (MAIT) cells are essential in defending against infection. Sepsis is a systemic inflammatory response to infection and a leading cause of death. The relationship between the overall competency of the host immune response and disease severity is not fully elucidated. This study identified a higher proportion of circulating MAIT17 with expression of IL-17A and retinoic acid receptor-related orphan receptor γt in patients with sepsis. The proportion of MAIT17 was correlated with the severity of sepsis. Single-cell RNA-sequencing analysis revealed an enhanced expression of lactate dehydrogenase A (LDHA) in MAIT17 in patients with sepsis. Cell-culture experiments demonstrated that phosphoinositide 3-kinase-LDHA signaling was required for retinoic acid receptor-related orphan receptor γt expression in MAIT17. Finally, the elevated levels of plasma IL-18 promoted the differentiation of circulating MAIT17 cells in sepsis. In summary, this study reveals a new role of circulating MAIT17 in promoting sepsis severity and suggests the phosphoinositide 3-kinase-LDHA signaling as a driving force in MAIT17 responses.


Subject(s)
Cell Differentiation , Mucosal-Associated Invariant T Cells , Sepsis , Humans , Sepsis/immunology , Sepsis/pathology , Sepsis/blood , Mucosal-Associated Invariant T Cells/immunology , Mucosal-Associated Invariant T Cells/metabolism , Male , Female , Middle Aged , Severity of Illness Index , Aged , Interleukin-17/metabolism , Interleukin-17/blood , Signal Transduction , Phosphatidylinositol 3-Kinases/metabolism
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