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T cells, as well as interleukins released by lymphocytes, can induce NPP formation of NPP ( + T cells, derived from splenocytes of acid-treated male mice, into nave mice, indicating that CD4 + T cells participate in FMS pathogenesis ( + mucosal-associated invariant T (MAIT) cells was increased in FMS patients with FMS and suggested this population as a potential biomarker ( + T cells, including IL-17A, IL-22, IL-9, TNF-, and IFN- ( + FOXP3 + ) was reduced, accompanied by increased IL-5 secretion from Th2 cells