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鉴定新生记忆 CD8 T 细胞及其发生过程建模。

Identification of Nascent Memory CD8 T Cells and Modeling of Their Ontogeny.

机构信息

Team Dracula, Inria, 69603 Villeurbanne, France; Institut Camille Jordan, Université de Lyon, Université Claude Bernard Lyon 1, CNRS UMR 5208, 43 Boulevard du 11 novembre 1918, 69622 Villeurbanne Cedex, France.

CIRI, ICL, INSERM U1111, Université Claude Bernard Lyon 1, CNRS UMR 5308, École Normale Supérieure de Lyon, Université de Lyon, 69007 Lyon, France.

出版信息

Cell Syst. 2017 Mar 22;4(3):306-317.e4. doi: 10.1016/j.cels.2017.01.014. Epub 2017 Feb 22.

DOI:10.1016/j.cels.2017.01.014
PMID:28237797
Abstract

Primary immune responses generate short-term effectors and long-term protective memory cells. The delineation of the genealogy linking naive, effector, and memory cells has been complicated by the lack of phenotypes discriminating effector from memory differentiation stages. Using transcriptomics and phenotypic analyses, we identify Bcl2 and Mki67 as a marker combination that enables the tracking of nascent memory cells within the effector phase. We then use a formal approach based on mathematical models describing the dynamics of population size evolution to test potential progeny links and demonstrate that most cells follow a linear naive→early effector→late effector→memory pathway. Moreover, our mathematical model allows long-term prediction of memory cell numbers from a few early experimental measurements. Our work thus provides a phenotypic means to identify effector and memory cells, as well as a mathematical framework to investigate their genealogy and to predict the outcome of immunization regimens in terms of memory cell numbers generated.

摘要

原发性免疫应答产生短期效应器和长期保护性记忆细胞。由于缺乏区分效应器和记忆分化阶段的表型,因此对连接幼稚、效应器和记忆细胞的谱系进行了描述。我们使用转录组学和表型分析,确定了 Bcl2 和 Mki67 作为标记组合,可用于在效应器阶段内跟踪新出现的记忆细胞。然后,我们使用基于描述群体大小演化动态的数学模型的正式方法来测试潜在的后代关系,并证明大多数细胞遵循线性幼稚→早期效应器→晚期效应器→记忆途径。此外,我们的数学模型允许从少数早期实验测量中对记忆细胞数量进行长期预测。因此,我们的工作提供了一种表型方法来识别效应器和记忆细胞,以及一种数学框架来研究它们的谱系,并根据生成的记忆细胞数量预测免疫接种方案的结果。

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