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基于分泌产物的单细胞分选用于功能定义的细胞治疗。

Single-cell sorting based on secreted products for functionally defined cell therapies.

作者信息

Miwa Hiromi, Dimatteo Robert, de Rutte Joseph, Ghosh Rajesh, Di Carlo Dino

机构信息

Department of Bioengineering, University of California - Los Angeles, Los Angeles, CA 90095 USA.

Department of Chemical and Biomolecular Engineering, University of California - Los Angeles, Los Angeles, CA 90095 USA.

出版信息

Microsyst Nanoeng. 2022 Jul 22;8:84. doi: 10.1038/s41378-022-00422-x. eCollection 2022.

Abstract

Cell therapies have emerged as a promising new class of "living" therapeutics over the last decade and have been particularly successful for treating hematological malignancies. Increasingly, cellular therapeutics are being developed with the aim of treating almost any disease, from solid tumors and autoimmune disorders to fibrosis, neurodegenerative disorders and even aging itself. However, their therapeutic potential has remained limited due to the fundamental differences in how molecular and cellular therapies function. While the structure of a molecular therapeutic is directly linked to biological function, cells with the same genetic blueprint can have vastly different functional properties (e.g., secretion, proliferation, cell killing, migration). Although there exists a vast array of analytical and preparative separation approaches for molecules, the functional differences among cells are exacerbated by a lack of functional potency-based sorting approaches. In this context, we describe the need for next-generation single-cell profiling microtechnologies that allow the direct evaluation and sorting of single cells based on functional properties, with a focus on secreted molecules, which are critical for the in vivo efficacy of current cell therapies. We first define three critical processes for single-cell secretion-based profiling technology: (1) partitioning individual cells into uniform compartments; (2) accumulating secretions and labeling via reporter molecules; and (3) measuring the signal associated with the reporter and, if sorting, triggering a sorting event based on these reporter signals. We summarize recent academic and commercial technologies for functional single-cell analysis in addition to sorting and industrial applications of these technologies. These approaches fall into three categories: microchamber, microfluidic droplet, and lab-on-a-particle technologies. Finally, we outline a number of unmet needs in terms of the discovery, design and manufacturing of cellular therapeutics and how the next generation of single-cell functional screening technologies could allow the realization of robust cellular therapeutics for all patients.

摘要

在过去十年中,细胞疗法已成为一类前景广阔的新型“活性”疗法,尤其在治疗血液系统恶性肿瘤方面取得了显著成功。越来越多的细胞疗法正在研发中,其目标是治疗几乎任何疾病,从实体瘤、自身免疫性疾病到纤维化、神经退行性疾病,甚至衰老本身。然而,由于分子疗法和细胞疗法作用方式的根本差异,它们的治疗潜力仍然有限。虽然分子疗法的结构与生物学功能直接相关,但具有相同基因蓝图的细胞可能具有截然不同的功能特性(例如,分泌、增殖、细胞杀伤、迁移)。尽管存在大量用于分子的分析和制备分离方法,但由于缺乏基于功能效力的分选方法,细胞之间的功能差异进一步加剧。在此背景下,我们描述了对下一代单细胞分析微技术的需求,这些技术能够基于功能特性对单细胞进行直接评估和分选,重点关注分泌分子,因为分泌分子对当前细胞疗法的体内疗效至关重要。我们首先定义了基于单细胞分泌分析技术的三个关键过程:(1)将单个细胞分隔到均匀的隔室中;(2)通过报告分子积累分泌物并进行标记;(3)测量与报告分子相关的信号,如果要进行分选,则根据这些报告分子信号触发分选事件。我们总结了近期用于功能单细胞分析的学术和商业技术,以及这些技术的分选和工业应用。这些方法可分为三类:微腔、微流控液滴和颗粒上实验室技术。最后,我们概述了细胞疗法在发现、设计和制造方面的一些未满足需求,以及下一代单细胞功能筛选技术如何能够为所有患者实现强大的细胞疗法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c675/9304353/ad13d3c88776/41378_2022_422_Fig1_HTML.jpg

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