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Percentage and function of CD4(+)CD25(+) regulatory T cells in patients with hyperthyroidism

The current study observed the percentage of peripheral blood (PB) CD4(+)CD25(+) regulatory T cells (Tregs) and the influence of CD4(+)CD25(+) Tregs on the proliferation of naïve CD4 T cells in patients with hyperthyroidism. Furthermore, preliminary discussions are presented on the action mechanism...

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Detalles Bibliográficos
Autores principales: Jiang, Ting-Jun, Cao, Xue-Liang, Luan, Sha, Cui, Wan-Hui, Qiu, Si-Huang, Wang, Yi-Chao, Zhao, Chang-Jiu, Fu, Peng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5783454/
https://www.ncbi.nlm.nih.gov/pubmed/29207121
http://dx.doi.org/10.3892/mmr.2017.8154
Descripción
Sumario:The current study observed the percentage of peripheral blood (PB) CD4(+)CD25(+) regulatory T cells (Tregs) and the influence of CD4(+)CD25(+) Tregs on the proliferation of naïve CD4 T cells in patients with hyperthyroidism. Furthermore, preliminary discussions are presented on the action mechanism of CD4(+)CD25(+) Tregs on hyperthyroidism attacks. The present study identified that compared with the percentage of PB CD4(+)CD25(+) Tregs in healthy control subjects, no significant changes were observed in the percentage of PB CD4(+)CD25(+) Tregs in patients with hyperthyroidism (P>0.05). For patients with hyperthyroidism, CD4(+)CD25(+) Tregs exhibited significantly reduced inhibition of the proliferation of naïve CD4 T cells and decreased secretion capacity on the cytokines of CD4 T cells, compared with those of healthy control subjects (P<0.05). In addition, it was demonstrated that thyroid function of patients with hyperthyroidism was significantly improved (P<0.05) subsequent to receiving medication. Compared with the percentage of PB CD4(+)CD25(+) Tregs in patients with hyperthyroidism before treatment, no significant changes were observed in the percentage of PB CD4(+)CD25(+) Tregs in hyperthyroidism patients following treatment (P>0.05). In the patients with hyperthyroidism, following treatment, CD4(+)CD25(+) Tregs exhibited significantly increased inhibition of the proliferation of naïve CD4 T cells and increased secretion capacity of CD4 T cell cytokines, compared with those of the patients with hyperthyroidism prior to treatment (P<0.05). PB CD4(+)CD25(+) Tregs function was decreased in patients with hyperthyroidism, and its non-proportional decrease may be closely associated with the occurrence and progression of hyperthyroidism.