Therapy of type 1 diabetes with CD4+CD25high CD127-regulatory T cells prolongs survival of pancreatic islets - Results of one year follow-up

被引:346
作者
Marek-Trzonkowska, Natalia [1 ]
Mysliwiec, Malgorzata [2 ]
Dobyszuk, Anita [3 ]
Grabowska, Marcelina [3 ]
Derkowska, Ilona [2 ]
Juscinska, Jolanta [4 ]
Owczuk, Radoslaw [5 ]
Szadkowska, Agnieszka [6 ]
Witkowski, Piotr [7 ]
Mlynarski, Wojciech [6 ]
Jarosz-Chobot, Przemyslawa [8 ]
Bossowski, Artur [9 ]
Siebert, Janusz [1 ]
Trzonkowski, Piotr [3 ]
机构
[1] Med Univ Gdansk, Dept Family Med, PL-80210 Gdansk, Poland
[2] Med Univ Gdansk, Dept Pediat Diabetol & Endocrinol, PL-80210 Gdansk, Poland
[3] Med Univ Gdansk, Dept Clin Immunol & Transplantol, PL-80210 Gdansk, Poland
[4] Reg Ctr Blood Donat & Treatment, PL-180210 Gdansk, Poland
[5] Med Univ Gdansk, Dept Anesthesiol & Crit Care, PL-80210 Gdansk, Poland
[6] Med Univ Lodz, Dept Pediat Oncol Hematol & Diabetol, PL-91738 Lodz, Poland
[7] Univ Chicago, Dept Surg, Sect Transplantat, Chicago, IL 60637 USA
[8] Med Univ Silesia, Dept Pediat Endocrinol & Diabet, PL-40055 Katowice, Poland
[9] Med Univ Bialystok, Dept Pediat Endocrinol & Diabetol, PL-15089 Bialystok, Poland
关键词
Type 1 diabetes mellitus; CD4+CD25+T regulatory cells; Tregs; Immunotherapy; REGULATORY CELLS; IMMUNOSENESCENCE; PLASTICITY; DISEASE;
D O I
10.1016/j.clim.2014.03.016
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
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 x 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 beta-cells in DM1 (registration: ISRCTN06128462). (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:23 / 30
页数:8
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