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Selective deletion of antigen-specific CD8+ T cells by MHC class I tetramers coupled to the type I ribosome-inactivating protein saporin.通过与 I 型核糖体失活蛋白皂草素偶联的 MHC I 类四聚体选择性删除抗原特异性 CD8 + T 细胞。
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HLA class I epitope discovery in type 1 diabetes.1型糖尿病中HLA I类表位的发现
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Antigen recognition induces phosphatidylserine exposure on the cell surface of human CD8+ T cells.抗原识别可诱导人CD8 + T细胞表面暴露磷脂酰丝氨酸。
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Membrane-bound CD95 ligand expressed on human antigen-presenting cells prevents alloantigen-specific T cell response without impairment of viral and third-party T cell immunity.人抗原呈递细胞上表达的膜结合型CD95配体可预防同种异体抗原特异性T细胞反应,而不会损害病毒和第三方T细胞免疫。
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TNF receptor superfamily-induced cell death: redox-dependent execution.肿瘤坏死因子受体超家族诱导的细胞死亡:氧化还原依赖性执行过程
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Autoimmunity in the era of genomics and proteomics.基因组学和蛋白质组学时代的自身免疫
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The evolution of adaptive immune systems.适应性免疫系统的进化
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Autoreactive CD8 T cells associated with beta cell destruction in type 1 diabetes.与1型糖尿病中β细胞破坏相关的自身反应性CD8 T细胞。
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9
CD8+ T cell-mediated HLA-A*0201-restricted cytotoxicity to transaldolase peptide 168-176 in patients with multiple sclerosis.多发性硬化症患者中CD8 + T细胞介导的针对转醛醇酶肽168 - 176的HLA - A*0201限制性细胞毒性作用
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How do CD4+CD25+ regulatory T cells control autoimmunity?CD4+CD25+调节性T细胞是如何控制自身免疫的?
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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.

DOI:10.1182/blood-2007-09-113522
PMID:18096763
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2275020/
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。