{"title":"Assessing Lupus-Like Disease in Murine Model Systems.","authors":"Hui Yin Lee, Teja Celhar, Anna-Marie Fairhurst","doi":"10.1002/cpz1.272","DOIUrl":null,"url":null,"abstract":"<p><p>Systemic Lupus Erythematosus (SLE) is a complex and heterogenous autoimmune disease, where genetics, immunology, and environmental factors all play a role. Murine models have contributed critical information on mechanisms of disease and prospective therapeutics. The key features that have been used to study the disease include the development of anti-nuclear autoantibodies (ANAs), splenomegaly, and kidney disease. The loss of tolerance and subsequent autoimmune features, and the progression to severe disease, are all dependent on immune dysregulation. In this article, we will describe the methods used to evaluate the underlying immunological features of the disease, as a more sensitive strategy to understand the disease itself and the mechanisms of potential novel therapeutics. © 2021 The Authors. Current Protocols published by Wiley Periodicals LLC. Basic Protocol 1: End study protocols for tissue harvesting Basic Protocol 2: End study protocols for tissue processing Basic Protocol 3: Immunophenotyping using flow cytometry protocols Support Protocol: Tissue processing for cold storage Basic Protocol 4: Additional tissue processing for later analyses Basic Protocol 5: Analysis of serum auto-antibodies by ELISAs (ANAs, snRNP, and dsDNA).</p>","PeriodicalId":11174,"journal":{"name":"Current Protocols","volume":"1 11","pages":"e272"},"PeriodicalIF":0.0000,"publicationDate":"2021-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/cpz1.272","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Systemic Lupus Erythematosus (SLE) is a complex and heterogenous autoimmune disease, where genetics, immunology, and environmental factors all play a role. Murine models have contributed critical information on mechanisms of disease and prospective therapeutics. The key features that have been used to study the disease include the development of anti-nuclear autoantibodies (ANAs), splenomegaly, and kidney disease. The loss of tolerance and subsequent autoimmune features, and the progression to severe disease, are all dependent on immune dysregulation. In this article, we will describe the methods used to evaluate the underlying immunological features of the disease, as a more sensitive strategy to understand the disease itself and the mechanisms of potential novel therapeutics. © 2021 The Authors. Current Protocols published by Wiley Periodicals LLC. Basic Protocol 1: End study protocols for tissue harvesting Basic Protocol 2: End study protocols for tissue processing Basic Protocol 3: Immunophenotyping using flow cytometry protocols Support Protocol: Tissue processing for cold storage Basic Protocol 4: Additional tissue processing for later analyses Basic Protocol 5: Analysis of serum auto-antibodies by ELISAs (ANAs, snRNP, and dsDNA).
在小鼠模型系统中评估狼疮样疾病。
系统性红斑狼疮(SLE)是一种复杂的异质自身免疫性疾病,遗传、免疫和环境因素都起着重要作用。小鼠模型在疾病机制和前瞻性治疗方面提供了重要信息。用于研究该疾病的关键特征包括抗核自身抗体(ANAs)的发展、脾肿大和肾脏疾病。耐受性的丧失和随后的自身免疫特征,以及向严重疾病的进展,都依赖于免疫失调。在这篇文章中,我们将描述用于评估疾病潜在免疫学特征的方法,作为一种更敏感的策略来了解疾病本身和潜在的新疗法的机制。©2021作者。当前协议由Wiley期刊有限责任公司发布。基本协议1:组织收获的结束研究协议基本协议2:组织处理的结束研究协议基本协议3:使用流式细胞术协议进行免疫表型分析支持协议:冷冻组织处理基本协议4:后续分析的额外组织处理基本协议5:通过elisa (ANAs, snRNP和dsDNA)分析血清自身抗体。
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