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用于转化免疫学的体外微生理模型。

In vitro micro-physiological models for translational immunology.

作者信息

Ramadan Qasem, Gijs Martin A M

机构信息

Bioelectronics Laboratory, Institute of Microelectronics, 11 Science Park II, Singapore 117685.

出版信息

Lab Chip. 2015 Feb 7;15(3):614-36. doi: 10.1039/c4lc01271b.

Abstract

The immune system is a source of regulation of the human body and is key for its stable functioning. Animal models have been successfully used for many years to study human immunity and diseases and provided significant contributions to the development of powerful new therapies. However, such models inevitably display differences from the human metabolism and disease state and therefore may correlate poorly with the human conditions. This explains the interest for the use of in vitro models of human cells, which have better potential to assist in understanding the physiological events that characterize the immune response in humans. Microfluidic technologies offer great capabilities to create miniaturized in vivo-like physiological models that mimic tissue-tissue interactions and simulate the body metabolism in both the healthy and diseased states. The micro-scale features of these microfluidic systems allow positioning heterogeneous cellular cultures in close proximity to each other in a dynamic fluidic environment, thereby allowing efficient cell-cell interactions and effectively narrowing the gap between in vivo and in vitro conditions. Due to the relative simplicity of these systems, compared to animal models, it becomes possible to investigate cell signaling by monitoring the metabolites transported from one tissue to another in real time. This allows studying detailed physiological events and in consequence understanding the influence of metabolites on a specific tissue/organ function as well as on the healthy/diseased state modulation. Numerous in vitro models of human organs have been developed during the last few years, aiming to mimic as closely as possible the in vivo characteristics of such organs. This technology is still in its infancy, but is promised a bright future in industrial and medical applications. Here we review the recent literature, in which functional microphysiological models have been developed to mimic tissues and to explore multi-tissue interactions, focusing in particular on the study of immune reactions, inflammation and the development of diseases. Also, an outlook on the opportunities and issues for further translational development of functional in vitro models in immunology will be presented.

摘要

免疫系统是人体调节的一个来源,对其稳定运作至关重要。多年来,动物模型已成功用于研究人类免疫和疾病,并为强大的新疗法的开发做出了重大贡献。然而,此类模型不可避免地与人类新陈代谢和疾病状态存在差异,因此与人类情况的相关性可能较差。这就解释了人们对使用人类细胞体外模型的兴趣,这类模型在协助理解表征人类免疫反应的生理事件方面具有更大潜力。微流控技术具有强大的能力,可创建小型化的类体内生理模型,模拟组织与组织之间的相互作用,并在健康和患病状态下模拟身体新陈代谢。这些微流控系统的微观特征允许在动态流体环境中将异质细胞培养物彼此紧密定位,从而实现高效的细胞间相互作用,并有效缩小体内和体外条件之间的差距。由于这些系统相对简单,与动物模型相比,通过实时监测从一个组织运输到另一个组织的代谢物来研究细胞信号传导成为可能。这有助于研究详细的生理事件,进而了解代谢物对特定组织/器官功能以及对健康/疾病状态调节的影响。在过去几年中,已经开发了许多人类器官的体外模型,旨在尽可能紧密地模拟此类器官的体内特征。这项技术仍处于起步阶段,但在工业和医学应用中前景光明。在这里,我们回顾了最近的文献,其中已开发出功能性微生理模型来模拟组织并探索多组织相互作用,特别关注免疫反应、炎症和疾病发展的研究。此外,还将展望功能性体外模型在免疫学中进一步转化发展的机遇和问题。

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