Secondary T cell-T cell synaptic interactions drive the differentiation of protective CD8+ T cells

被引:123
作者
Gerard, Audrey [1 ]
Khan, Omar [1 ]
Beemiller, Peter [1 ]
Oswald, Erin [1 ]
Hu, Joyce [2 ]
Matloubian, Mehrdad [2 ]
Krummel, Matthew F. [1 ]
机构
[1] Univ Calif San Francisco, Dept Pathol, San Francisco, CA 94140 USA
[2] Univ Calif San Francisco, Dept Med, Div Rheumatol, San Francisco, CA USA
基金
美国国家卫生研究院;
关键词
LYMPH-NODES; DENDRITIC CELLS; IMMUNOLOGICAL SYNAPSE; IMMUNE-RESPONSE; NAIVE CELLS; MEMORY; EFFECTOR; INFECTION; DYNAMICS; PROLIFERATION;
D O I
10.1038/ni.2547
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Immunization results in the differentiation of CD8(+) T cells, such that they acquire effector abilities and convert into a memory pool. Priming of T cells takes place via an immunological synapse formed with an antigen-presenting cell (APC). By disrupting synaptic stability at different times, we found that the differentiation of CD8(+) T cells required cell interactions beyond those made with APCs. We identified a critical differentiation period that required interactions between primed T cells. We found that T cell-T cell synapses had a major role in the generation of protective CD8(+) T cell memory. T cell-T cell synapses allowed T cells to polarize critical secretion of interferon-gamma (IFN-gamma) toward each other. Collective activation and homotypic clustering drove cytokine sharing and acted as regulatory stimuli for T cell differentiation.
引用
收藏
页码:356 / 363
页数:8
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