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免疫性疾病和精准医学的人源化小鼠模型。

Humanized mouse models of immunological diseases and precision medicine.

机构信息

The Jackson Laboratory, 600 Main Street, Bar Harbor, ME, 04609, USA.

The Jackson Laboratory, 1650 Santa Ana Avenue, Sacramento, CA, 95838, USA.

出版信息

Mamm Genome. 2019 Jun;30(5-6):123-142. doi: 10.1007/s00335-019-09796-2. Epub 2019 Mar 7.

Abstract

With the increase in knowledge resulting from the sequencing of the human genome, the genetic basis for the underlying differences in individuals, their diseases, and how they respond to therapies is starting to be understood. This has formed the foundation for the era of precision medicine in many human diseases that is beginning to be implemented in the clinic, particularly in cancer. However, preclinical testing of therapeutic approaches based on individual biology will need to be validated in animal models prior to translation into patients. Although animal models, particularly murine models, have provided significant information on the basic biology underlying immune responses in various diseases and the response to therapy, murine and human immune systems differ markedly. These fundamental differences may be the underlying reason why many of the positive therapeutic responses observed in mice have not translated directly into the clinic. There is a critical need for preclinical animal models in which human immune responses can be investigated. For this, many investigators are using humanized mice, i.e., immunodeficient mice engrafted with functional human cells, tissues, and immune systems. We will briefly review the history of humanized mice, the remaining limitations, approaches to overcome them and how humanized mouse models are being used as a preclinical bridge in precision medicine for evaluation of human therapies prior to their implementation in the clinic.

摘要

随着人类基因组测序带来的知识增长,个体之间潜在差异、疾病以及对治疗反应的遗传基础开始被理解。这为许多人类疾病的精准医学时代奠定了基础,该时代开始在临床上实施,特别是在癌症领域。然而,基于个体生物学的治疗方法的临床前测试需要在转化为患者之前在动物模型中进行验证。尽管动物模型,特别是鼠模型,为各种疾病的免疫反应基础生物学和治疗反应提供了重要信息,但鼠类和人类的免疫系统有显著差异。这些根本差异可能是许多在小鼠中观察到的积极治疗反应未能直接转化为临床的原因。迫切需要能够研究人类免疫反应的临床前动物模型。为此,许多研究人员正在使用人源化小鼠,即植入功能性人类细胞、组织和免疫系统的免疫缺陷小鼠。我们将简要回顾人源化小鼠的历史、尚存的局限性、克服这些局限性的方法以及人源化小鼠模型如何作为精准医学的临床前桥梁,在将治疗方法应用于临床之前评估人类治疗方法。

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