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体外从脐血 CD34+ 造血祖细胞生成人类树突状细胞亚群。

In Vitro Generation of Human Dendritic Cell Subsets from CD34+ Cord Blood Progenitors.

机构信息

Institut Cochin, INSERM U1016, CNRS UMR8104, Université de Paris Cité, Paris, France.

King's College London, Centre for Inflammation Biology and Cancer Immunology, London, UK.

出版信息

Methods Mol Biol. 2023;2618:121-132. doi: 10.1007/978-1-0716-2938-3_9.

Abstract

Dendritic cells (DCs) are professional antigen-presenting cells controlling the activation of T cells and thus regulating adaptive immune response against pathogens or tumors. Modeling human DC differentiation and function is crucial for our understanding of immune response and the development of new therapies. Considering DC rarity in human blood, in vitro systems allowing their faithful generation are needed. This chapter will describe a DC differentiation method based on the co-culture of CD34 cord blood progenitors together with mesenchymal stromal cells (eMSCs) engineered to deliver growth factors and chemokines.

摘要

树突状细胞(DCs)是专业的抗原呈递细胞,控制着 T 细胞的激活,从而调节针对病原体或肿瘤的适应性免疫反应。模拟人类 DC 分化和功能对于我们理解免疫反应和开发新疗法至关重要。考虑到人类血液中 DC 的稀有性,需要有能够忠实生成它们的体外系统。本章将描述一种基于 CD34 脐血祖细胞与工程化的间充质基质细胞(eMSCs)共培养的 DC 分化方法,该方法可以传递生长因子和趋化因子。

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