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Humanized Mouse Models of Rheumatoid Arthritis for Studies on Immunopathogenesis and Preclinical Testing of Cell-Based Therapies

机译:类风湿关节炎的人源化小鼠模型用于免疫病理学研究和基于细胞的疗法的临床前测试

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摘要

Rodent models of rheumatoid arthritis (RA) have been used over decades to study the immunopathogenesis of the disease and to explore intervention strategies. Nevertheless, mouse models of RA reach their limit when it comes to testing of new therapeutic approaches such as cell-based therapies. Differences between the human and the murine immune system make it difficult to draw reliable conclusions about the success of immunotherapies. To overcome this issue, humanized mouse models have been established that mimic components of the human immune system in mice. Two main strategies have been pursued for humanization: the introduction of human transgenes such as human leukocyte antigen molecules or specific T cell receptors, and the generation of mouse/human chimera by transferring human cells or tissues into immunodeficient mice. Recently, both approaches have been combined to achieve more sophisticated humanized models of autoimmune diseases. This review discusses limitations of conventional mouse models of RA-like disease and provides a closer look into studies in humanized mice exploring their usefulness and necessity as preclinical models for testing of cell-based therapies in autoimmune diseases such as RA.
机译:类风湿关节炎(RA)的啮齿动物模型已经使用了数十年,以研究该疾病的免疫发病机制并探索干预策略。然而,在测试新的治疗方法(例如基于细胞的治疗)时,RA的小鼠模型已达到其极限。人类和鼠类免疫系统之间的差异使得很难得出有关免疫疗法成功的可靠结论。为了克服这个问题,已经建立了模仿小鼠中人类免疫系统成分的人源化小鼠模型。追求人性化的两种主要策略是:引入人类转基因,例如人类白细胞抗原分子或特定的T细胞受体,以及通过将人类细胞或组织转移到免疫缺陷小鼠中来产生小鼠/人类嵌合体。近来,两种方法已被组合以实现自身免疫性疾病的更复杂的人源化模型。这篇综述讨论了传统的类RA小鼠模型的局限性,并提供了对人源化小鼠研究的更深入研究,探索它们作为临床前模型来测试自身免疫性疾病(如RA)中基于细胞的疗法的有效性和必要性。

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