Department of Immunology and Microbiology, School of Life Science, Beijing University of Chinese Medicine, Beijing, China.
Experimental Research Center, China Academy of Chinese Medical Sciences, Beijing, China.
J Cosmet Dermatol. 2024 Jul;23(7):2478-2489. doi: 10.1111/jocd.16279. Epub 2024 Apr 5.
Skin 16S microbiome diversity analysis indicates that the Staphylococcus genus, especially Staphylococcus aureus (S. aureus), plays a crucial role in the inflammatory lesions of acne. However, current animal models for acne do not fully replicate human diseases, especially pustular acne, which limits the development of anti-acne medications.
The aim is to develop a mouse model for acne, establishing an animal model that more closely mimics the clinical presentation of pustular acne. This will provide a new research platform for screening anti-acne drugs and evaluating the efficacy of clinical anti-acne experimental treatments.
Building upon the existing combination of acne-associated Cutibacterium acnes (C. acnes) with artificial sebum, we will inject a mixture of S. aureus and C. acnes locally into the dermis in a 3:7 ratio.
We found that the acne animal model with mixed bacterial infection better replicates the dynamic evolution process of human pustular acne. Compared to the infection with C. acnes alone, mixed bacterial infection resulted in pustules with a distinct yellowish appearance, resembling pustular acne morphology. The lesions exhibited redness, vascular dilation, and noticeable congestion, along with evident infiltration of inflammatory cells. This induced higher levels of inflammation, as indicated by a significant increase in the secretion of inflammatory factors such as IL-1β and TNF-α.
This model can reflect the clinical symptoms and development of human pustular acne, overcoming the limitations of animal models commonly used in basic research to study this situation. It provides support for foundational research and the development of new acne medications.
皮肤 16S 微生物多样性分析表明,葡萄球菌属,尤其是金黄色葡萄球菌(S. aureus),在痤疮的炎症病变中起着关键作用。然而,目前的痤疮动物模型不能完全复制人类疾病,尤其是脓疱性痤疮,这限制了抗痤疮药物的发展。
目的是开发一种痤疮的小鼠模型,建立一种更能模拟脓疱性痤疮临床表现的动物模型。这将为筛选抗痤疮药物和评估临床抗痤疮实验治疗的疗效提供一个新的研究平台。
在现有的痤疮相关的痤疮丙酸杆菌(C. acnes)与人工皮脂联合应用的基础上,我们将以 3:7 的比例将金黄色葡萄球菌和 C. acnes 的混合物局部注射到真皮中。
我们发现混合细菌感染的痤疮动物模型更好地复制了人类脓疱性痤疮的动态演变过程。与单独感染 C. acnes 相比,混合细菌感染导致脓疱呈现出明显的黄色外观,类似于脓疱性痤疮的形态。病变表现出红肿、血管扩张和明显的充血,以及明显的炎症细胞浸润。这导致了更高水平的炎症,表现为促炎因子如 IL-1β和 TNF-α的分泌显著增加。
该模型可以反映人类脓疱性痤疮的临床症状和发展,克服了用于研究这种情况的基础研究中常用的动物模型的局限性。它为基础研究和新的痤疮药物的开发提供了支持。