Trogocytosis of chimeric antigen receptors between T cells is regulated by their transmembrane domains

被引:1
|
作者
Barbera, Stefano [1 ]
Schuiling, Matthijs J. A. [1 ]
Sanjaya, Nathaniel A. [1 ]
Pietilae, Ilkka
Saren, Tina [1 ]
Essand, Magnus [1 ]
Dimberg, Anna [1 ]
机构
[1] Uppsala Univ, Dept Immunol Genet & Pathol, Sci Life Lab, Uppsala, Sweden
基金
瑞典研究理事会;
关键词
MHC CLASS-II; MEMBRANE-FRAGMENTS; SURFACE MOLECULES; TARGET-CELLS; CAPTURE; COMPLEXES; PROTEIN;
D O I
10.1126/sciimmunol.ado2054
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Trogocytosis is an exchange of membrane-associated molecules between cells that can either halt or boost immune responses. However, the mechanism that regulates trogocytosis in T cells and its consequences are not yet clear. Here, we demonstrate that T cells can exchange chimeric antigen receptors (CARs) by trogocytosis, thereby arming recipient T cells with the capacity to respond to tumor antigens by up-regulating proteins associated with a cytotoxic response and killing of target cells. We demonstrate that although trogocytosis is dependent on cell-cell contact, the exchange of a specific cell membrane protein does not require a cognate binding partner on the surface of recipient cells. Instead, the probability that a protein is exchanged by trogocytosis is determined by its transmembrane domain. This finding opens new avenues for modulating this process in CAR-T cells.
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页数:13
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