细胞毒性T细胞
细胞生物学
串扰
启动(农业)
抗原提呈细胞
T细胞
免疫系统
树突状细胞
抗原
获得性免疫系统
化学
生物
免疫学
体外
生物化学
物理
发芽
植物
光学
作者
Claire Hivroz,Karine Chemin,Marie Tourret,Armelle Bohineust
标识
DOI:10.1615/critrevimmunol.v32.i2.30
摘要
Dendritic cells (DCs) are professional antigen-presenting cells (APCs) with the unique property of inducing priming and differentiation of naïve CD4+ and CD8+ T cells into helper and cytotoxic effectors. Their efficiency is due to their unique ability to process antigen, express costimulatory molecules, secrete cytokines, and migrate to tissues or lymphoid organs to prime T cells. DCs also play an important role in T-cell peripheral tolerance. There is ample evidence that the DC ability to present antigens is regulated by CD4+ helper T cells. Indeed, interactions between surface receptors and ligands expressed respectively by T cells and DCs, as well as T-cell-derived cytokines modify DC functions. This T-cell-induced modification of DCs has been called "education" or "licensing." This intimate crosstalk between DCs and T lymphocytes is key in establishing appropriate adaptive immune responses. It requires cognate interactions between T lymphocytes and DCs, which are organized in time and space by structures called immunological synapses. Here we discuss the particular aspects of immunological synapses formed between T cells and DCs and the role these organized interactions have in T-cell-DC crosstalk.
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