S94 COVID-19感染中中性粒细胞反应功能失调因亚型而异

O. Thein, K. Belchamber, A. Faniyi, J. Hazeldine, F. Grudzinska, MJ Hughes, AE Jasper, L. Crowley, K. Yip, S. Lugg, E. Sapey, D. Parekh, D. Thickett, A. Scott
{"title":"S94 COVID-19感染中中性粒细胞反应功能失调因亚型而异","authors":"O. Thein, K. Belchamber, A. Faniyi, J. Hazeldine, F. Grudzinska, MJ Hughes, AE Jasper, L. Crowley, K. Yip, S. Lugg, E. Sapey, D. Parekh, D. Thickett, A. Scott","doi":"10.1136/thorax-2022-btsabstracts.100","DOIUrl":null,"url":null,"abstract":"S94 Figure 1Comparison of neutrophil effector functions between COVID-19 variants (alpha n=33, delta n=13, omicron n-14). A.% change in phagocytosis significantly increased between alpha and delta patients (p=0.0162). B. Fold change in cells migrated through a transwell pore to IL8 compared to vehicle control significantly reduced in omicron patients compared alpha and delta (vs alpha p=0.0018, vs delta p=0.0370). C. Neutrophil extracellular trap production after stimulation with PMA compared to vehicle control significantly reduced in omicron patients compared to alpha (p=0.0396)[Figure omitted. See PDF]DiscussionOur results showing changes in neutrophil „function and phenotype differ between variants of COVID-19 infection, potentially reflect viral evolution. This change in neutrophil function may contribute to the evolving clinical phenotype observed in patients. Our population of ward-based COVID-19 patients represents the majority of inpatient hospital burden where early intervention may prevent clinical deterioration. Targeting neutrophil function may be an effective way of improving infection outcome in the future.ReferenceBelchamber K, et al. Altered neutrophil phenotype and function in non-ICU hospitalised COVID-19 patients correlated with disease severity. medRxiv, 2021: p. 2021.06.08.21258535.","PeriodicalId":426518,"journal":{"name":"‘The Terminator’ – Neutrophils in respiratory disease","volume":"40 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2022-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"S94 Dysfunctional neutrophil response in COVID-19 infection vary by subtype\",\"authors\":\"O. Thein, K. Belchamber, A. Faniyi, J. Hazeldine, F. Grudzinska, MJ Hughes, AE Jasper, L. Crowley, K. Yip, S. Lugg, E. Sapey, D. Parekh, D. Thickett, A. Scott\",\"doi\":\"10.1136/thorax-2022-btsabstracts.100\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"S94 Figure 1Comparison of neutrophil effector functions between COVID-19 variants (alpha n=33, delta n=13, omicron n-14). A.% change in phagocytosis significantly increased between alpha and delta patients (p=0.0162). B. Fold change in cells migrated through a transwell pore to IL8 compared to vehicle control significantly reduced in omicron patients compared alpha and delta (vs alpha p=0.0018, vs delta p=0.0370). C. Neutrophil extracellular trap production after stimulation with PMA compared to vehicle control significantly reduced in omicron patients compared to alpha (p=0.0396)[Figure omitted. See PDF]DiscussionOur results showing changes in neutrophil „function and phenotype differ between variants of COVID-19 infection, potentially reflect viral evolution. This change in neutrophil function may contribute to the evolving clinical phenotype observed in patients. Our population of ward-based COVID-19 patients represents the majority of inpatient hospital burden where early intervention may prevent clinical deterioration. Targeting neutrophil function may be an effective way of improving infection outcome in the future.ReferenceBelchamber K, et al. Altered neutrophil phenotype and function in non-ICU hospitalised COVID-19 patients correlated with disease severity. medRxiv, 2021: p. 2021.06.08.21258535.\",\"PeriodicalId\":426518,\"journal\":{\"name\":\"‘The Terminator’ – Neutrophils in respiratory disease\",\"volume\":\"40 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-11-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"‘The Terminator’ – Neutrophils in respiratory disease\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1136/thorax-2022-btsabstracts.100\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"‘The Terminator’ – Neutrophils in respiratory disease","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1136/thorax-2022-btsabstracts.100","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

图1 COVID-19变异之间中性粒细胞效应功能的比较(α n=33, δ n=13,组粒n-14)。A. α和δ患者的吞噬百分率变化显著增加(p=0.0162)。B.与对照物相比,组微粒患者通过井间孔迁移到il - 8的细胞折叠变化与α和δ相比显著减少(α p=0.0018, δ p=0.0370)。C.与对照组相比,经PMA刺激后,组微粒患者的中性粒细胞胞外陷阱生成显著减少(p=0.0396)[图略]。我们的研究结果显示,中性粒细胞功能和表型的变化在COVID-19感染的变体之间存在差异,这可能反映了病毒的进化。这种中性粒细胞功能的改变可能有助于患者观察到的临床表型的演变。我们的病房COVID-19患者群体代表了住院患者负担的大部分,早期干预可以防止临床恶化。靶向中性粒细胞功能可能是未来改善感染结果的有效途径。参考文献belchamber K等。非icu住院COVID-19患者中性粒细胞表型和功能改变与疾病严重程度相关中华医学杂志,2021:p. 2021.06.08.21258535。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
S94 Dysfunctional neutrophil response in COVID-19 infection vary by subtype
S94 Figure 1Comparison of neutrophil effector functions between COVID-19 variants (alpha n=33, delta n=13, omicron n-14). A.% change in phagocytosis significantly increased between alpha and delta patients (p=0.0162). B. Fold change in cells migrated through a transwell pore to IL8 compared to vehicle control significantly reduced in omicron patients compared alpha and delta (vs alpha p=0.0018, vs delta p=0.0370). C. Neutrophil extracellular trap production after stimulation with PMA compared to vehicle control significantly reduced in omicron patients compared to alpha (p=0.0396)[Figure omitted. See PDF]DiscussionOur results showing changes in neutrophil „function and phenotype differ between variants of COVID-19 infection, potentially reflect viral evolution. This change in neutrophil function may contribute to the evolving clinical phenotype observed in patients. Our population of ward-based COVID-19 patients represents the majority of inpatient hospital burden where early intervention may prevent clinical deterioration. Targeting neutrophil function may be an effective way of improving infection outcome in the future.ReferenceBelchamber K, et al. Altered neutrophil phenotype and function in non-ICU hospitalised COVID-19 patients correlated with disease severity. medRxiv, 2021: p. 2021.06.08.21258535.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
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:604180095
Book学术官方微信