Designer T cells by T cell receptor replacement

被引:83
|
作者
Sommermeyer, Daniel
Neudorfer, Julia
Weinhold, Monika
Leisegang, Matthias
Engels, Boris
Noessner, Elfriede
Heemskerk, Mirjam H. M.
Charo, Jehad
Schendel, Dolores J.
Blankenstein, Thomas
Bernhard, Helga
Uckert, Wolfgang
机构
[1] Max Delbruck Ctr Mol Med, D-13092 Berlin, Germany
[2] Tech Univ Munich, Klinikum Rechts Isar, Dept Hematol Oncol, D-8000 Munich, Germany
[3] Inst Immunol, Berlin, Germany
[4] Humboldt Univ, Inst Biol, D-1086 Berlin, Germany
[5] GSF Natl Res Ctr Environm & Hlth, Inst Mol Immunol, Munich, Germany
[6] Leiden Univ, Ctr Med, Dept Hematol, Lab Expt Hematol, NL-2300 RA Leiden, Netherlands
[7] GSF Natl Res Ctr Environm & Hlth, Clin Cooperat Grp Antigen Specif Immunotherapy, Munich, Germany
[8] Tech Univ Munich, D-8000 Munich, Germany
关键词
gene therapy; T cells; TCR; TCR replacement;
D O I
10.1002/eji.200636539
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
T cell receptor (TCR) gene transfer is a convenient method to produce antigen-specific T cells for adoptive therapy. However, the expression of two TCR in T cells could impair their function or cause unwanted effects by mixed TCR heterodimers. With five different TCR and four different T cells, either mouse or human, we show that some TCR are strong - in terms of cell surface expression - and replace weak TCR on the cell surface, resulting in exchange of antigen specificity. Two strong TCR are co-expressed. A mouse TCR replaces human TCR on human T cells. Even though it is still poorly understood why some TCR alpha/beta combinations are preferentially expressed on T cells, our data suggest that, in the future, designer T cells with exclusive tumor reactivity can be generated by T cell engineering.
引用
收藏
页码:3052 / 3059
页数:8
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