Animal models of psoriasis for novel drug discovery: a literature update
- Zih-Chan Lin 1, Shih-Chun Yang 2, Thi Thu Phuong Tran 3, Jia-You Fang 4,5,6
- 1Chronic Diseases and Health Promotion Research Center, Chang Gung University of Science and Technology, Puzi, Taiwan.
- 2Department of Microbiology, Soochow University, Taipei, Taiwan.
- 3Department of Life Sciences, University of Science and Technology of Hanoi, Hanoi, Vietnam.
- 4Pharmaceutics Laboratory, Graduate Institute of Natural Products, Chang Gung University, Taoyuan, Taiwan.
- 5Research Center for Food and Cosmetic Safety and Center for Drug Research and Development, Chang Gung University of Science and Technology, Taoyuan, Taiwan.
- 6Department of Anesthesiology, Chang Gung Memorial Hospital, Taoyuan, Taiwan.
- 0Chronic Diseases and Health Promotion Research Center, Chang Gung University of Science and Technology, Puzi, Taiwan.
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Summary
This summary is machine-generated.This review evaluates preclinical psoriasis models, finding no single system perfectly mimics the human condition. Combining complementary models and advanced techniques like CRISPR/Cas9 is crucial for future therapeutic development in psoriasis research.
Area Of Science
- Dermatology and immunology research focusing on preclinical models for psoriasis.
Background
- Psoriasis is a chronic, immune-mediated inflammatory skin disease with complex pathogenesis.
- Effective therapeutics depend on preclinical models that accurately replicate disease mechanisms.
Purpose Of The Study
- To review and evaluate current in vivo psoriasis models.
- To assess the utility of gene editing technologies in model development.
- To highlight limitations and future directions for psoriasis research models.
Main Methods
- Comprehensive literature search of PubMed, Scopus, and Google Scholar (Jan 2015-Mar 2025).
- Evaluation of spontaneous mutation, transgenic, knockout, xenotransplantation, cytokine-induced, and imiquimod-induced models.
- Assessment of CRISPR/Cas9 gene editing applications in creating targeted psoriasis models.
Main Results
- No single in vivo model fully replicates human psoriasis.
- Imiquimod-induced models are practical but better represent acute inflammation.
- Key histological and immunological features of psoriasis are variably reproduced across models.
Conclusions
- Multimodel validation strategies are essential for translational relevance.
- Humanized systems and genome editing advancements hold promise for future research.
- Combining complementary models and human-derived components can enhance translational applicability.
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