Question-Driven Selection of Psoriasis Animal Models: A Structured Narrative Review of 48 Model Records.

IF 4.6 2区 医学 Q2 IMMUNOLOGY
Journal of Inflammation Research Pub Date : 2026-10-12 eCollection Date: 2026-01-01 DOI:10.2147/JIR.S641713
Tong Zhao, Xianbin Zhao, Donglian Du, Zehua Qin, Songqi Tang, Min Xiao
{"title":"Question-Driven Selection of Psoriasis Animal Models: A Structured Narrative Review of 48 Model Records.","authors":"Tong Zhao, Xianbin Zhao, Donglian Du, Zehua Qin, Songqi Tang, Min Xiao","doi":"10.2147/JIR.S641713","DOIUrl":null,"url":null,"abstract":"<p><p>Animal models connect psoriasis mechanisms to preclinical testing, but no model is informative for every question. This structured narrative review used PubMed, supplemented by reference-list screening and manual checks, to identify 29 original studies contributing 48 model records. One reviewer conducted screening and extraction, with targeted verification by a second reviewer. Within the selected records, IMQ- and IL-23-induced models primarily addressed acute inflammatory pathways, genetically engineered and composite models tested defined perturbations, humanized models examined human immune responses, and relapse models examined post-resolution reactivation. Composite designs were the largest category (22/48, 45.8%), whereas TRM were experimentally assessed in 6/48 (12.5%). We integrated model construction, disease-stage suitability and mechanism-evidence patterns into a conceptual question-driven framework linking prespecified objectives to candidate initial models, complementary validation and interpretation boundaries. The framework is a hypothesis-generating planning aid that has not undergone independent validation. Focused questions may be addressed with a single model, whereas complex mechanistic or translational questions require complementary models and comparison with human data.</p>","PeriodicalId":16107,"journal":{"name":"Journal of Inflammation Research","volume":"19 ","pages":"641713"},"PeriodicalIF":4.6000,"publicationDate":"2026-10-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13674558/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Inflammation Research","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.2147/JIR.S641713","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Animal models connect psoriasis mechanisms to preclinical testing, but no model is informative for every question. This structured narrative review used PubMed, supplemented by reference-list screening and manual checks, to identify 29 original studies contributing 48 model records. One reviewer conducted screening and extraction, with targeted verification by a second reviewer. Within the selected records, IMQ- and IL-23-induced models primarily addressed acute inflammatory pathways, genetically engineered and composite models tested defined perturbations, humanized models examined human immune responses, and relapse models examined post-resolution reactivation. Composite designs were the largest category (22/48, 45.8%), whereas TRM were experimentally assessed in 6/48 (12.5%). We integrated model construction, disease-stage suitability and mechanism-evidence patterns into a conceptual question-driven framework linking prespecified objectives to candidate initial models, complementary validation and interpretation boundaries. The framework is a hypothesis-generating planning aid that has not undergone independent validation. Focused questions may be addressed with a single model, whereas complex mechanistic or translational questions require complementary models and comparison with human data.

银屑病动物模型的问题驱动选择:48个模型记录的结构化叙述回顾。
动物模型将牛皮癣机制与临床前测试联系起来,但没有一个模型能回答所有问题。这篇结构化的叙述性综述使用PubMed,辅以参考文献列表筛选和人工检查,确定了29项原始研究,贡献了48条模型记录。一位审稿人进行筛选和提取,由另一位审稿人进行有针对性的验证。在选定的记录中,IMQ-和il -23诱导的模型主要解决急性炎症途径,基因工程和复合模型测试定义的扰动,人源化模型检查人类免疫反应,复发模型检查解决后再激活。复合设计是最大的类别(22/48,45.8%),而TRM是实验评估的6/48(12.5%)。我们将模型构建、疾病阶段适用性和机制-证据模式整合到一个概念性问题驱动的框架中,将预先指定的目标与候选初始模型、互补验证和解释边界联系起来。该框架是一种未经独立验证的假设生成规划辅助工具。重点问题可以用单一模型解决,而复杂的机制或翻译问题需要补充模型并与人类数据进行比较。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Journal of Inflammation Research
Journal of Inflammation Research Immunology and Microbiology-Immunology
CiteScore
6.10
自引率
2.20%
发文量
658
审稿时长
16 weeks
期刊介绍: An international, peer-reviewed, open access, online journal that welcomes laboratory and clinical findings on the molecular basis, cell biology and pharmacology of inflammation.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书