Mouse Models of Alopecia Areata: C3H/HeJ Mice Versus the Humanized AA Mouse Model

Q2 Medicine
Amos Gilhar , Rimma Laufer Britva , Aviad Keren , Ralf Paus
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引用次数: 0

Abstract

The C3H/HeJ model has long dominated basic alopecia areata (AA) in vivo research and has been used as proof-of-principle that Jak inhibitors are suitable agents for AA management in vivo. However, its histologic features are not typical of human AA, and it is questionable whether it is sufficiently clinically predictive for evaluating the therapeutic effects of candidate AA agents. Instead, the humanized mouse model of AA has been used to functionally demonstrate the role of key immune cells in AA pathogenesis and to discover human-specific pharmacologic targets in AA management. Therefore, we advocate the use of both models in future preclinical AA research.

斑秃小鼠模型:C3H/HeJ小鼠与人源化AA小鼠模型
C3H/HeJ模型长期以来主导着基础斑秃(AA)的体内研究,并被用作Jak抑制剂是体内AA治疗的合适药物的原理证明。然而,其组织学特征并非人类AA的典型特征,因此是否足以用于临床预测评估候选AA药物的治疗效果尚存疑问。相反,AA人源化小鼠模型已被用于功能性地证明关键免疫细胞在AA发病机制中的作用,并发现AA治疗中人类特异性的药理学靶点。因此,我们提倡在未来的临床前AA研究中同时使用这两种模型。
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期刊介绍: Journal of Investigative Dermatology Symposium Proceedings (JIDSP) publishes peer-reviewed, invited papers relevant to all aspects of cutaneous biology and skin disease. Papers in the JIDSP are often initially presented at a scientific meeting. Potential topics include biochemistry, biophysics, carcinogenesis, cellular growth and regulation, clinical research, development, epidemiology and other population-based research, extracellular matrix, genetics, immunology, melanocyte biology, microbiology, molecular and cell biology, pathology, pharmacology and percutaneous absorption, photobiology, physiology, and skin structure.
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