Eosinophils and T cell surface molecule transcript levels in the blood differentiate eosinophilic esophagitis (EoE) from GERD.

Sathisha Upparahalli Venkateshaiah, Hemanth Kumar Kandikattu, Chandra Sekhar Yadavalli, Anil Mishra
{"title":"Eosinophils and T cell surface molecule transcript levels in the blood differentiate eosinophilic esophagitis (EoE) from GERD.","authors":"Sathisha Upparahalli Venkateshaiah,&nbsp;Hemanth Kumar Kandikattu,&nbsp;Chandra Sekhar Yadavalli,&nbsp;Anil Mishra","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>We recently rereported that blood mRNA levels of T cells and IgE receptors are the novel non-invasive biomarkers for eosinophilic esophagitis (EoE) with the aim to establish the panel of T cells and IgE receptor as the novel non-invasive biomarkers for EoE. In addition to earlier proposed cell surface molecules, we now added T cell receptor CXCR6 and eosinophils expressed cell surface molecules CD101 and CD274 mRNA levels. The mRNA levels of eosinophils cell surface molecule CD101 and CD274 and T cell receptor CXCR6, Vβ11, CD1d and chemokine CXCL16 levels were examined using the blood of normal, EoE and GERD patients. The analysis showed statistically significant induced mRNA levels of CD274, CD101 and reduced CXCR6 will be an additional molecule with respective 95%, 90% and 90% positive predictive value in between EoE and GERD patients. In brief, these additional data will be critical to establish a complete panel of earlier published TCRδ (95%), Jα18 (83%) and FCεRII (100%) non-invasive biomarker to monitor the EoE severity and treatment effect in EoE patients. In conclusion, we now propose both induced and reduced transcript levels of cell surface molecules of the cell surface molecules along with earlier reported molecules that will be useful for monitoring EoE status before and following treatment. Most importantly, the complete predictive non-invasive biomarker panel will also serve to differentiate EoE from GERD.</p>","PeriodicalId":73425,"journal":{"name":"International journal of basic and clinical immunology","volume":"4 1-2","pages":"1-8"},"PeriodicalIF":0.0000,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8457322/pdf/nihms-1739511.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International journal of basic and clinical immunology","FirstCategoryId":"1085","ListUrlMain":"","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

We recently rereported that blood mRNA levels of T cells and IgE receptors are the novel non-invasive biomarkers for eosinophilic esophagitis (EoE) with the aim to establish the panel of T cells and IgE receptor as the novel non-invasive biomarkers for EoE. In addition to earlier proposed cell surface molecules, we now added T cell receptor CXCR6 and eosinophils expressed cell surface molecules CD101 and CD274 mRNA levels. The mRNA levels of eosinophils cell surface molecule CD101 and CD274 and T cell receptor CXCR6, Vβ11, CD1d and chemokine CXCL16 levels were examined using the blood of normal, EoE and GERD patients. The analysis showed statistically significant induced mRNA levels of CD274, CD101 and reduced CXCR6 will be an additional molecule with respective 95%, 90% and 90% positive predictive value in between EoE and GERD patients. In brief, these additional data will be critical to establish a complete panel of earlier published TCRδ (95%), Jα18 (83%) and FCεRII (100%) non-invasive biomarker to monitor the EoE severity and treatment effect in EoE patients. In conclusion, we now propose both induced and reduced transcript levels of cell surface molecules of the cell surface molecules along with earlier reported molecules that will be useful for monitoring EoE status before and following treatment. Most importantly, the complete predictive non-invasive biomarker panel will also serve to differentiate EoE from GERD.

血液中嗜酸性粒细胞和T细胞表面分子转录水平可区分嗜酸性食管炎(EoE)和胃食管反流。
我们最近报道了血液中T细胞和IgE受体的mRNA水平是嗜酸性粒细胞性食管炎(EoE)的新的无创生物标志物,目的是建立T细胞和IgE受体的小组作为EoE的新的无创生物标志物。除了之前提出的细胞表面分子,我们现在添加了T细胞受体CXCR6和嗜酸性粒细胞表达细胞表面分子CD101和CD274 mRNA水平。采用正常、EoE和GERD患者血液检测嗜酸性粒细胞细胞表面分子CD101和CD274 mRNA水平及T细胞受体CXCR6、Vβ11、CD1d和趋化因子CXCL16水平。分析显示,在EoE和GERD患者中,诱导的CD274、CD101和减少的CXCR6 mRNA水平将是具有统计学意义的额外分子,分别为95%、90%和90%的阳性预测值。总之,这些额外的数据对于建立一个完整的早期发表的TCRδ(95%)、Jα18(83%)和FCεRII(100%)的无创生物标志物来监测EoE患者的严重程度和治疗效果至关重要。总之,我们现在提出了诱导和降低细胞表面分子转录水平的细胞表面分子以及早期报道的分子,这些分子将有助于监测治疗前后的EoE状态。最重要的是,完整的预测性非侵入性生物标志物面板也将用于区分EoE和GERD。
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
自引率
0.00%
发文量
0
×
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:481959085
Book学术官方微信