Killer Artificial Antigen Presenting Cells (KaAPC) for Efficient In Vitro Depletion of Human Antigen-specific T Cells

被引:8
|
作者
Schuetz, Christian [1 ]
Fleck, Martin [2 ,3 ]
Schneck, Jonathan P. [1 ]
Oelke, Mathias [1 ]
机构
[1] Johns Hopkins Univ, Inst Cell Engn, Dept Pathol, Baltimore, MD 21218 USA
[2] Univ Regensburg, Dept Internal Med 1, D-93053 Regensburg, Germany
[3] Asklepios Med Ctr, Dept Rheumatol, Chicago, IL USA
来源
关键词
Immunology; Issue; 90; Autoimmunity; Apoptosis; antigen-specific CD8+T cells; HLA-A2-Ig; Fas/FasL; KaAPC; DENDRITIC CELLS; ELIMINATION; DISEASES;
D O I
10.3791/51859
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Current treatment of T cell mediated autoimmune diseases relies mostly on strategies of global immunosuppression, which, in the long term, is accompanied by adverse side effects such as a reduced ability to control infections or malignancies. Therefore, new approaches need to be developed that target only the disease mediating cells and leave the remaining immune system intact. Over the past decade a variety of cell based immunotherapy strategies to modulate T cell mediated immune responses have been developed. Most of these approaches rely on tolerance-inducing antigen presenting cells (APC). However, in addition to being technically difficult and cumbersome, such cellbased approaches are highly sensitive to cytotoxic T cell responses, which limits their therapeutic capacity. Here we present a protocol for the generation of non-cellular killer artificial antigen presenting cells (KaAPC), which allows for the depletion of pathologic T cells while leaving the remaining immune system untouched and functional. KaAPC is an alternative solution to cellular immunotherapy which has potential for treating autoimmune diseases and allograft rejections by regulating undesirable T cell responses in an antigen specific fashion.
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页数:5
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