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从溃疡性结肠炎患者的白细胞分离产物中制备功能保存的CD4+ CD25高调节性T细胞,适用于调节性T细胞转移疗法。

Preparation of functionally preserved CD4+ CD25high regulatory T cells from leukapheresis products from ulcerative colitis patients, applicable to regulatory T-cell transfer therapy.

作者信息

Sumida Y, Nakamura K, Kanayama K, Akiho H, Teshima T, Takayanagi R

机构信息

Department of Medicine and Bioregulatory Science, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.

出版信息

Cytotherapy. 2008;10(7):698-710. doi: 10.1080/14653240802345812.

Abstract

BACKGROUND

Ulcerative colitis (UC) is an intractable disease; therefore new therapies need to be developed. CD4(+) CD25(high) regulatory T cells (Treg) significantly ameliorate colitis in animal models. In active UC patients, although Treg are functionally preserved, their proportion in peripheral blood decreases. Thus Treg transfer therapy is expected to be efficacious for UC. During leukapheresis for UC, Treg are depleted, as well as colitogenic effector leukocytes. We therefore designed a leukapheresis/Treg transfer therapy in which Treg are isolated from leukapheresis products and transfused to patients, and studied large-scale germ-free methods of Treg preparation.

METHODS

Using the CliniMACS cell selection system, we conducted Treg isolation experiments from leukapheresis products in which B and CD8(+) T cells were depleted, followed by positive selection of CD25(+) cells. In some experiments, isolated Treg or non-Treg were expanded with interleukin-2 (IL-2) +/- transforming growth factor (TGF)-beta1. Expression of a Treg-specific marker, FOXP3, and gut-homing receptors, and suppressor activity of isolated or cultured cells, were analyzed.

RESULTS

CD4(+) CD25(high) T cells were collected and efficiently enriched with a good recovery rate. Isolated cells preferentially expressed FOXP3 and significantly suppressed T-cell proliferation in vitro. In addition, isolated Treg could be efficiently expanded, and Treg could be induced from non-Treg with TGF-beta1 in vitro. TGF-beta1 significantly up-regulated alphaEbeta7 and alpha4beta7 integrins.

DISCUSSION

We have established a method of Treg isolation from leukapheresis products that can be used clinically; therefore, Treg transfer therapy is feasible in combination with leukapheresis for UC. Expansion or induction of Treg in vitro may be another approach to Treg-based immunotherapy.

摘要

背景

溃疡性结肠炎(UC)是一种难治性疾病,因此需要开发新的治疗方法。CD4(+) CD25(高表达)调节性T细胞(Treg)在动物模型中可显著改善结肠炎。在活动期UC患者中,尽管Treg功能保留,但外周血中其比例下降。因此,Treg转移疗法有望对UC有效。在UC患者进行白细胞单采时,Treg以及致结肠炎效应白细胞均会被清除。因此,我们设计了一种白细胞单采/Treg转移疗法,即从白细胞单采产物中分离Treg并输给患者,并研究了大规模无菌制备Treg的方法。

方法

使用CliniMACS细胞分选系统,我们从已清除B细胞和CD8(+) T细胞的白细胞单采产物中进行Treg分离实验,随后对CD25(+)细胞进行阳性分选。在一些实验中,分离出的Treg或非Treg用白细胞介素-2(IL-2)±转化生长因子(TGF)-β1进行扩增。分析分离或培养细胞的Treg特异性标志物FOXP3、肠道归巢受体的表达以及抑制活性。

结果

收集到了CD4(+) CD25(高表达) T细胞,并以良好的回收率有效富集。分离出的细胞优先表达FOXP3,并在体外显著抑制T细胞增殖。此外,分离出的Treg可有效扩增,并且在体外可通过TGF-β1从非Treg诱导出Treg。TGF-β1显著上调αEβ7和α4β7整合素。

讨论

我们建立了一种可用于临床的从白细胞单采产物中分离Treg的方法;因此,Treg转移疗法与UC白细胞单采联合应用是可行的。体外扩增或诱导Treg可能是基于Treg的免疫治疗的另一种方法。

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