Author/Authors :
Lee، نويسنده , , Jin-Soo and Lee، نويسنده , , Wonwoo and Kim، نويسنده , , Sang-Hyun and Kang، نويسنده , , Youna and Lee، نويسنده , , Naeun and Shin، نويسنده , , Min-Sun and Kang، نويسنده , , Seong Wook and Kang، نويسنده , , Insoo، نويسنده ,
Abstract :
Th17 cells produce IL-17 that plays an important role in host defense. However, little is known about whether aging affects human Th17 cells. Here we demonstrated that healthy elderly people (age ≥ 65) had a decreased frequency of IL-17-producing cells in memory CD4+ T cells compared to healthy young people (age ≤ 40) while both groups had similar frequencies of IFN-γ-producing cells in the same memory cell subset as measured by flow cytometry. In contrast, the healthy elderly had increased differentiation of IL-17-producing effector cells but not IFN-γ-producing cells from naive CD4+ T cells compared to the healthy young. The results of ELISA also showed similar findings with increased IL-17 production from naive CD4+ T cells and decreased IL-17 production from memory CD4+ T cells in the elderly compared to the young. These findings indicate that aging differentially affects naive and memory Th17 cell responses in humans.
Keywords :
CD4+ T cells , aging , human , IL-17 , T helper 17 (Th17) cells