FOXP3型
医学
1型糖尿病
胰岛
白细胞介素2受体
胰岛素
小岛
糖尿病
调节性T细胞
内科学
不利影响
免疫学
内分泌学
免疫系统
T细胞
作者
Natalia Marek-Trzonkowska,Małgorzata Myśliwiec,Anita Dobyszuk,Marcelina Grabowska,Ilona Derkowska,Jolanta Juścińska,Radosław Owczuk,Agnieszka Szadkowska,Piotr Witkowski,Wojciech Młynarski,Przemysława Jarosz‐Chobot,Artur Bossowski,Janusz Siebert,Piotr Trzonkowski
标识
DOI:10.1016/j.clim.2014.03.016
摘要
It is hypothesized that CD4(+)CD25(+)FoxP3(+) regulatory T cells (Tregs) can prevent destruction of pancreatic islets protecting from type 1 diabetes (DM1). Here we present results of one year follow-up of 12 DM1 children treated with autologous expanded ex vivo Tregs. Patients received either a single or double Tregs infusion up to the total dose of 30×10(6)/kg. No severe adverse effects were observed. The treatment did not impair post-immunization antibody responses. Tregs infusion was followed by increase in Tregs number in peripheral blood. Most of the patients responded to the therapy with increase in C-peptide levels (8/12 and 4/6 after the first and the second dose, respectively). Tregs administration resulted also in lower requirement for exogenous insulin (8/12 treated patients versus 2/10 untreated controls in remission) with two children completely insulin independent at one year. Repetitive administration of Tregs is safe and can prolong survival of β-cells in DM1 (registration: ISRCTN06128462).
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