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杀伤性人工抗原呈递细胞:一种清除特定T细胞的新策略。

Killer artificial antigen-presenting cells: a novel strategy to delete specific T cells.

作者信息

Schütz Christian, Fleck Martin, Mackensen Andreas, Zoso Alessia, Halbritter Dagmar, Schneck Jonathan P, Oelke Mathias

机构信息

Department of Internal Medicine I, University of Regensburg, Germany.

出版信息

Blood. 2008 Apr 1;111(7):3546-52. doi: 10.1182/blood-2007-09-113522. Epub 2007 Dec 20.

Abstract

Several cell-based immunotherapy strategies have been developed to specifically modulate T cell-mediated immune responses. These methods frequently rely on the utilization of tolerogenic cell-based antigen-presenting cells (APCs). However, APCs are highly sensitive to cytotoxic T-cell responses, thus limiting their therapeutic capacity. Here, we describe a novel bead-based approach to modulate T-cell responses in an antigen-specific fashion. We have generated killer artificial APCs (kappaaAPCs) by coupling an apoptosis-inducing alpha-Fas (CD95) IgM mAb together with HLA-A2 Ig molecules onto beads. These kappaaAPCs deplete targeted antigen-specific T cells in a Fas/Fas ligand (FasL)-dependent fashion. T-cell depletion in cocultures is rapidly initiated (30 minutes), dependent on the amount of kappaaAPCs and independent of activation-induced cell death (AICD). kappaaAPCs represent a novel technology that can control T cell-mediated immune responses, and therefore has potential for use in treatment of autoimmune diseases and allograft rejection.

摘要

已经开发了几种基于细胞的免疫疗法策略来特异性调节T细胞介导的免疫反应。这些方法通常依赖于使用耐受性的基于细胞的抗原呈递细胞(APC)。然而,APC对细胞毒性T细胞反应高度敏感,从而限制了它们的治疗能力。在这里,我们描述了一种基于珠子的新方法,以抗原特异性方式调节T细胞反应。我们通过将诱导凋亡的α-Fas(CD95)IgM单克隆抗体与HLA-A2 Ig分子偶联到珠子上,生成了杀伤性人工APC(kappaaAPC)。这些kappaaAPC以Fas/Fas配体(FasL)依赖的方式耗尽靶向抗原特异性T细胞。共培养中的T细胞耗竭迅速开始(30分钟),取决于kappaaAPC的数量,并且独立于活化诱导的细胞死亡(AICD)。kappaaAPC代表了一种可以控制T细胞介导的免疫反应的新技术,因此具有用于治疗自身免疫性疾病和同种异体移植排斥反应的潜力。

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