银屑病疾病模型

疾病简介

银屑病(psoriasis)是一种常见并易复发的慢性炎症性皮肤病,具有特征性红色丘疹、斑块及银白色鳞屑,顽固难治,频繁复发,罹患终身等特点,其发病原因及发病机制均尚未完全明晰,目前认为是遗传和环境因素共同作用导致。

疾病模型

南模生物长期致力于自身免疫性疾病相关研究,开发了多种银屑病小鼠模型,为相关药物的药效评估和安全性评价提供了强有力的工具。

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Fig.1 Body weight (A) and body weight change (B) of IMQ induced Psoriasis model in hIL17A/hIL17F mice. (n=6). 

Test article 1 and test article 2 are from a collaborator.

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Fig.2 IMQ induced Psoriasis model in hIL17A/hIL17F mice. (A) ear thickness (B) skin thickness (C) clinical score (n=6). 

Test article 1 and test article 2 are from a collaborator. Mean ± SEM. t-test, *P < 0.05, **P < 0.01, ***P < 0.001.

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Fig.3 IMQ induced Psoriasis model in hIL17A/hIL17F mice. 

At the study endpoint, back skin samples were harvested and stained with H&E. Representative H&E staining images of the back skin from mice and histological changes were quantified using Baker system.  Results indicated that Bimekizumab significantly reduced skin lesions in IMQ induced Psoriasis model in hIL17A/hIL17F mice (n=6). 

Test article 1 and test article 2 are from a collaborator. Mean ± SEM. t-test, ***P < 0.001.

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Fig.4 IMQ induced Psoriasis model in hIL17A/hIL17F mice. 

At the study endpoint, back skin samples were harvested and hIL17F was tested by qPCR. Results indicated that Bimekizumab significantly reduced hIL17F expression level in IMQ induced Psoriasis model in hIL17A/hIL17F mice(n=6). 

Test article 1 and test article 2 are from a collaborator. Mean ± SEM. t-test, *P < 0.05.

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Fig.1 IMQ induced Psoriasis model in Balb/c. (A) body weight and (B) body weight change. *P<0.05, **P<0.01, ***P<0.001 vs G2.

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Fig.2 IMQ induced Psoriasis model in Balb/c. (A) ear thickness (B) skin thickness (C) cumulative score of PASI. ***P<0.001, *P<0.05 vs G2.

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Fig.3 IMQ induced Psoriasis model in Balb/c. (A) erythema score, (B) skin thickness score and (C) scabby score. ***P<0.001, **P<0.01, *P<0.05 vs G2.

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Fig.4 IMQ induced Psoriasis model in Balb/c. (A) spleen weight, (B) spleen index, (C) spleen image and (D) dorsal image on day3. ***P<0.001 vs G2.

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Fig.5 IMQ induced Psoriasis model in Balb/c. (A) serum TNF-α, (B) serum IL-23 and (C) serum IL-17A. ***P<0.001,  *P<0.05 vs G2.

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Fig.6 IMQ induced Psoriasis model in Balb/c. (A) Tnf-α (B) Il-23 (C) Il-17 mRNA expression of skin. (n=5). ***P<0.001, **P<0.01 vs G2.

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Fig.7 IMQ induced Psoriasis model in Balb/c. (A) Pathological Score (B) Epidermis thickness (C) typical pathology image. ****P<0.001, **P<0.01 vs G2.

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Fig.1 IMQ induced Psoriasis model based on hIL23A mice.

  • Rat IL-23因子诱导的SD大鼠银屑病模型

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Fig.1 rIL23-induced Psoriasis model in SD Rat. (A) Body weight. (B) Body weight change.

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Fig.2 rIL23-induced Psoriasis model in SD Rat. (A) Ear thickness. (B) Ear thickness change. (C) PASI score.

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Fig.3 Representative photo of rIL23-induced Psoriasis model in SD Rat. 

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Fig.4 rIL23-induced Psoriasis model in SD Rat. (A) Representative photo of H&E staining. (B) Baker score. 


  • Human IL-23因子诱导的SD大鼠银屑病模型

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Fig.1 hIL23-induced Psoriasis model in SD Rat. (A) Body weight. (B) Body weight change.

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Fig.2 hIL23-induced Psoriasis model in SD Rat. (A) Ear thickness. (B) Ear thickness change. (C) PASI score.

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Fig.3 Representative photo of hIL23-induced Psoriasis model in SD Rat.

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Fig.4 hIL23-induced Psoriasis model in SD Rat. (A) Representative photo of H&E staining. (B) Baker score. 

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