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Deciphering new mechanisms on T-cell costimulation by human mast cells
被引:3
|作者:
Frossi, Barbara
[1
]
Mion, Francesca
[1
]
Pucillo, Carlo
[1
]
机构:
[1] Univ Udine, Dept Med & Biol Sci, Immunol Lab, I-33100 Udine, Italy
关键词:
APC;
costimulation;
mast cell;
T-cell activation;
LANGERHANS CELLS;
DIFFERENTIATION;
STIMULATION;
SUPERFAMILY;
CHEMOKINES;
TOLERANCE;
MOLECULES;
IMMUNITY;
D O I:
10.1002/eji.201646390
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
It is well established that full activation of T cells to recognize a specific antigen requires additional signals. These secondary signals are generated by the interaction of costimulatory molecules expressed on APCs. Classical APCs include DCs, macrophages, Langerhans cells, and B cells. However, in recent years, several haematopoietic and nonhaematopoietic cells have been described to express MHC class II antigens and, in appropriate conditions, costimulatory molecules. In this issue, Suurmond et al. [Eur. J. Immunol. 2016. 46: 1132-1141] show, for the first time, that human mast cells not only express costimulatory molecules of the TNF-receptor and CD28 families, but can also costimulate T cells through a yet-to-be-defined CD28-independent interaction.
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页码:1105 / 1108
页数:4
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