April L Raftery, Céline Pattaroni, Nicola L Harris, Evelyn Tsantikos, Margaret L Hibbs
{"title":"影响并发肠道和肺部炎症的环境和炎症因素。","authors":"April L Raftery, Céline Pattaroni, Nicola L Harris, Evelyn Tsantikos, Margaret L Hibbs","doi":"10.1007/s00011-024-01953-x","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Crohn's disease and chronic obstructive pulmonary disease (COPD) are chronic inflammatory diseases that affect the gut and lung respectively and can occur comorbidly.</p><p><strong>Methods: </strong>Using the SHIP-1<sup>-/-</sup> model of Crohn's-like ileitis and chronic lung inflammation, the two diseases were co-investigated.</p><p><strong>Results: </strong>Contrary to prior literature, Crohn's-like ileitis was not fully penetrant in SHIP-1<sup>-/-</sup> mice, and housing in a specific pathogen-free facility was completely protective. Indeed, ileal tissue from SHIP-1<sup>-/-</sup> mice without overt ileitis was similar to control ilea. However, SHIP-1<sup>-/-</sup> mice with ileitis exhibited increased granulocytes in ileal tissue together with T cell lymphopenia and they lacked low abundance Bifidobacteria, suggesting this bacterium protects against ileitis. Lung disease, as defined by inflammation in lung washes, emphysema, and lung consolidation, was present in SHIP-1<sup>-/-</sup> mice regardless of ileitis phenotype; however, there was a shift in the nature of lung inflammation in animals with ileitis, with increased G-CSF and neutrophils, in addition to type 2 cytokines and eosinophils. Deficiency of G-CSF, which protects against lung disease, protected against the development of ileitis in SHIP-1<sup>-/-</sup> mice.</p><p><strong>Conclusions: </strong>These studies have defined environmental, immune, and inflammatory factors that predispose to ileitis, and have identified that comorbid lung disease correlates with a granulocyte signature.</p>","PeriodicalId":13550,"journal":{"name":"Inflammation Research","volume":" ","pages":""},"PeriodicalIF":4.8000,"publicationDate":"2024-10-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Environmental and inflammatory factors influencing concurrent gut and lung inflammation.\",\"authors\":\"April L Raftery, Céline Pattaroni, Nicola L Harris, Evelyn Tsantikos, Margaret L Hibbs\",\"doi\":\"10.1007/s00011-024-01953-x\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Crohn's disease and chronic obstructive pulmonary disease (COPD) are chronic inflammatory diseases that affect the gut and lung respectively and can occur comorbidly.</p><p><strong>Methods: </strong>Using the SHIP-1<sup>-/-</sup> model of Crohn's-like ileitis and chronic lung inflammation, the two diseases were co-investigated.</p><p><strong>Results: </strong>Contrary to prior literature, Crohn's-like ileitis was not fully penetrant in SHIP-1<sup>-/-</sup> mice, and housing in a specific pathogen-free facility was completely protective. Indeed, ileal tissue from SHIP-1<sup>-/-</sup> mice without overt ileitis was similar to control ilea. However, SHIP-1<sup>-/-</sup> mice with ileitis exhibited increased granulocytes in ileal tissue together with T cell lymphopenia and they lacked low abundance Bifidobacteria, suggesting this bacterium protects against ileitis. Lung disease, as defined by inflammation in lung washes, emphysema, and lung consolidation, was present in SHIP-1<sup>-/-</sup> mice regardless of ileitis phenotype; however, there was a shift in the nature of lung inflammation in animals with ileitis, with increased G-CSF and neutrophils, in addition to type 2 cytokines and eosinophils. Deficiency of G-CSF, which protects against lung disease, protected against the development of ileitis in SHIP-1<sup>-/-</sup> mice.</p><p><strong>Conclusions: </strong>These studies have defined environmental, immune, and inflammatory factors that predispose to ileitis, and have identified that comorbid lung disease correlates with a granulocyte signature.</p>\",\"PeriodicalId\":13550,\"journal\":{\"name\":\"Inflammation Research\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":4.8000,\"publicationDate\":\"2024-10-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Inflammation Research\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1007/s00011-024-01953-x\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CELL BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Inflammation Research","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s00011-024-01953-x","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0
摘要
背景:克罗恩病和慢性阻塞性肺疾病(COPD)是分别影响肠道和肺部的慢性炎症性疾病,可同时发生:方法:利用SHIP-1-/-克罗恩回肠炎和慢性肺部炎症模型,对这两种疾病进行联合研究:结果:与之前的文献相反,克罗恩病样回肠炎在SHIP-1-/-小鼠中并不具有完全的渗透性,而饲养在特定的无病原体设施中则具有完全的保护性。事实上,没有明显回肠炎的SHIP-1-/-小鼠的回肠组织与对照组回肠组织相似。然而,患有回肠炎的 SHIP-1-/- 小鼠回肠组织中的粒细胞增多,同时出现 T 细胞淋巴细胞减少症,而且它们缺乏低丰度双歧杆菌,这表明双歧杆菌对回肠炎有保护作用。无论回肠炎表型如何,SHIP-1-/-小鼠都会出现肺部疾病,表现为肺洗液中的炎症、肺气肿和肺固缩;然而,回肠炎动物肺部炎症的性质发生了变化,除了 2 型细胞因子和嗜酸性粒细胞外,G-CSF 和中性粒细胞也增加了。G-CSF对肺部疾病有保护作用,而SHIP-1-/-小鼠缺乏G-CSF则可防止回肠炎的发生:这些研究确定了易导致回肠炎的环境、免疫和炎症因素,并发现合并肺部疾病与粒细胞特征相关。
Environmental and inflammatory factors influencing concurrent gut and lung inflammation.
Background: Crohn's disease and chronic obstructive pulmonary disease (COPD) are chronic inflammatory diseases that affect the gut and lung respectively and can occur comorbidly.
Methods: Using the SHIP-1-/- model of Crohn's-like ileitis and chronic lung inflammation, the two diseases were co-investigated.
Results: Contrary to prior literature, Crohn's-like ileitis was not fully penetrant in SHIP-1-/- mice, and housing in a specific pathogen-free facility was completely protective. Indeed, ileal tissue from SHIP-1-/- mice without overt ileitis was similar to control ilea. However, SHIP-1-/- mice with ileitis exhibited increased granulocytes in ileal tissue together with T cell lymphopenia and they lacked low abundance Bifidobacteria, suggesting this bacterium protects against ileitis. Lung disease, as defined by inflammation in lung washes, emphysema, and lung consolidation, was present in SHIP-1-/- mice regardless of ileitis phenotype; however, there was a shift in the nature of lung inflammation in animals with ileitis, with increased G-CSF and neutrophils, in addition to type 2 cytokines and eosinophils. Deficiency of G-CSF, which protects against lung disease, protected against the development of ileitis in SHIP-1-/- mice.
Conclusions: These studies have defined environmental, immune, and inflammatory factors that predispose to ileitis, and have identified that comorbid lung disease correlates with a granulocyte signature.
期刊介绍:
Inflammation Research (IR) publishes peer-reviewed papers on all aspects of inflammation and related fields including histopathology, immunological mechanisms, gene expression, mediators, experimental models, clinical investigations and the effect of drugs. Related fields are broadly defined and include for instance, allergy and asthma, shock, pain, joint damage, skin disease as well as clinical trials of relevant drugs.