• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

粒细胞髓系来源抑制细胞水平低可能是严重 COVID-19 患者随访中生存的良好标志物。

Low Levels of Granulocytic Myeloid-Derived Suppressor Cells May Be a Good Marker of Survival in the Follow-Up of Patients With Severe COVID-19.

机构信息

Department of Laboratory Medicine, Virgen Macarena University Hospital, Seville, Spain.

Department of Medical Biochemistry and Molecular Biology, School of Medicine, University of Seville, Seville, Spain.

出版信息

Front Immunol. 2022 Jan 28;12:801410. doi: 10.3389/fimmu.2021.801410. eCollection 2021.

DOI:10.3389/fimmu.2021.801410
PMID:35154077
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8835351/
Abstract

Infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) causes a disease (coronavirus disease 2019, COVID-19) that may develop into a systemic disease with immunosuppression and death in its severe form. Myeloid-derived suppressive cells (MDSCs) are inhibitory cells that contribute to immunosuppression in patients with cancer and infection. Increased levels of MDSCs have been found in COVID-19 patients, although their role in the pathogenesis of severe COVID-19 has not been clarified. For this reason, we raised the question whether MDSCs could be useful in the follow-up of patients with severe COVID-19 in the intensive care unit (ICU). Thus, we monitored the immunological cells, including MDSCs, in 80 patients admitted into the ICU. After 1, 2, and 3 weeks, we examined for a possible association with mortality (40 patients). Although the basal levels of circulating MDSCs did not discriminate between the two groups of patients, the last measurement before the endpoint (death or ICU discharge) showed that patients discharged alive from the ICU had lower levels of granulocytic MDSCs (G-MDSCs), higher levels of activated lymphocytes, and lower levels of exhausted lymphocytes compared with patients who had a bad evolution (death). In conclusion, a steady increase of G-MDSCs during the follow-up of patients with severe COVID-19 was found in those who eventually died.

摘要

严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)感染可导致疾病(2019 年冠状病毒病,COVID-19),在严重感染形式下可能发展为伴有免疫抑制和死亡的全身性疾病。髓系来源的抑制细胞(MDSCs)是抑制性细胞,可导致癌症和感染患者的免疫抑制。在 COVID-19 患者中发现 MDSCs 水平升高,尽管其在严重 COVID-19 发病机制中的作用尚未阐明。因此,我们提出了一个问题,即 MDSCs 是否可以在重症 COVID-19 患者的 ICU 随访中发挥作用。因此,我们监测了包括 MDSCs 在内的 80 名 ICU 入院患者的免疫细胞。在第 1、2 和 3 周后,我们检查了它们与死亡率(40 名患者)的可能相关性。虽然循环 MDSCs 的基础水平不能区分两组患者,但在终点(死亡或 ICU 出院)之前的最后一次测量显示,从 ICU 出院存活的患者的粒性 MDSCs(G-MDSCs)水平较低,活化淋巴细胞水平较高,耗竭性淋巴细胞水平较低,而病情恶化(死亡)的患者则相反。总之,在对严重 COVID-19 患者进行随访期间,最终死亡的患者体内 G-MDSCs 持续增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfce/8835351/94f35c0db90c/fimmu-12-801410-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfce/8835351/c22c604a8acd/fimmu-12-801410-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfce/8835351/9c7e04731a82/fimmu-12-801410-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfce/8835351/925677c7245c/fimmu-12-801410-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfce/8835351/94f35c0db90c/fimmu-12-801410-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfce/8835351/c22c604a8acd/fimmu-12-801410-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfce/8835351/9c7e04731a82/fimmu-12-801410-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfce/8835351/925677c7245c/fimmu-12-801410-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfce/8835351/94f35c0db90c/fimmu-12-801410-g004.jpg

相似文献

1
Low Levels of Granulocytic Myeloid-Derived Suppressor Cells May Be a Good Marker of Survival in the Follow-Up of Patients With Severe COVID-19.粒细胞髓系来源抑制细胞水平低可能是严重 COVID-19 患者随访中生存的良好标志物。
Front Immunol. 2022 Jan 28;12:801410. doi: 10.3389/fimmu.2021.801410. eCollection 2021.
2
Increased Blood Monocytic Myeloid Derived Suppressor Cells but Low Regulatory T Lymphocytes in Patients with Mild COVID-19.轻度 COVID-19 患者血液中单核细胞来源的髓样抑制细胞增加,但调节性 T 淋巴细胞减少。
Viral Immunol. 2021 Nov;34(9):639-645. doi: 10.1089/vim.2021.0044. Epub 2021 Sep 16.
3
Mild and Asymptomatic COVID-19 Convalescents Present Long-Term Endotype of Immunosuppression Associated With Neutrophil Subsets Possessing Regulatory Functions.轻度和无症状 COVID-19 恢复期患者表现出与具有调节功能的中性粒细胞亚群相关的长期免疫抑制终末表型。
Front Immunol. 2021 Sep 29;12:748097. doi: 10.3389/fimmu.2021.748097. eCollection 2021.
4
Myeloid-Derived Suppressor Cells as a Potential Biomarker and Therapeutic Target in COVID-19.髓系来源的抑制细胞作为 COVID-19 的潜在生物标志物和治疗靶点。
Front Immunol. 2021 Jun 18;12:697405. doi: 10.3389/fimmu.2021.697405. eCollection 2021.
5
Expansion of myeloid-derived suppressor cells in patients with severe coronavirus disease (COVID-19).骨髓来源的抑制性细胞在重症冠状病毒病(COVID-19)患者中的扩增。
Cell Death Differ. 2020 Nov;27(11):3196-3207. doi: 10.1038/s41418-020-0572-6. Epub 2020 Jun 8.
6
Circulating myeloid-derived suppressor cells may be a useful biomarker in the follow-up of unvaccinated COVID-19 patients after hospitalization.循环髓系来源的抑制性细胞可能是 COVID-19 未接种疫苗患者出院后随访的一个有用的生物标志物。
Front Immunol. 2023 Nov 14;14:1266659. doi: 10.3389/fimmu.2023.1266659. eCollection 2023.
7
Elevated frequencies of CD14HLA-DR MDSCs in COVID-19 patients.新冠病毒肺炎患者中CD14+HLA-DR髓系来源抑制细胞频率升高。
Aging (Albany NY). 2021 Feb 26;13(5):6236-6246. doi: 10.18632/aging.202571.
8
CD4+ T effector memory cell dysfunction is associated with the accumulation of granulocytic myeloid-derived suppressor cells in glioblastoma patients.CD4 + T效应记忆细胞功能障碍与胶质母细胞瘤患者中粒细胞性髓源性抑制细胞的积累有关。
Neuro Oncol. 2016 Jun;18(6):807-18. doi: 10.1093/neuonc/nov280. Epub 2015 Nov 17.
9
Correlation of myeloid-derived suppressor cells with C-reactive protein, ferritin and lactate dehydrogenase levels in patients with severe COVID-19.重症 COVID-19 患者骨髓源性抑制细胞与 C 反应蛋白、铁蛋白和乳酸脱氢酶水平的相关性。
Scand J Immunol. 2022 Jan;95(1):e13108. doi: 10.1111/sji.13108. Epub 2021 Oct 15.
10
Severe COVID-19 Is Characterized by an Impaired Type I Interferon Response and Elevated Levels of Arginase Producing Granulocytic Myeloid Derived Suppressor Cells.严重的 COVID-19 表现为 I 型干扰素反应受损和产生精氨酸酶的粒细胞髓系来源抑制细胞水平升高。
Front Immunol. 2021 Jul 14;12:695972. doi: 10.3389/fimmu.2021.695972. eCollection 2021.

引用本文的文献

1
DAP1-2: a synthetic peptide targeting IL-1R1 receptor effectively suppresses IL-1β in vitro.DAP1-2:一种靶向 IL-1R1 受体的合成肽,可有效抑制体外的 IL-1β。
Immunol Res. 2024 Aug;72(4):788-796. doi: 10.1007/s12026-024-09485-6. Epub 2024 May 2.
2
The Functional Roles of MDSCs in Severe COVID-19 Pathogenesis.髓系来源抑制细胞在重症 COVID-19 发病机制中的功能作用。
Viruses. 2023 Dec 23;16(1):27. doi: 10.3390/v16010027.
3
Circulating myeloid-derived suppressor cells may be a useful biomarker in the follow-up of unvaccinated COVID-19 patients after hospitalization.

本文引用的文献

1
Increased Blood Monocytic Myeloid Derived Suppressor Cells but Low Regulatory T Lymphocytes in Patients with Mild COVID-19.轻度 COVID-19 患者血液中单核细胞来源的髓样抑制细胞增加,但调节性 T 淋巴细胞减少。
Viral Immunol. 2021 Nov;34(9):639-645. doi: 10.1089/vim.2021.0044. Epub 2021 Sep 16.
2
Management of infectious complications associated with coronavirus infection in severe patients admitted to ICU.重症监护病房收治的冠状病毒感染患者感染相关并发症的管理。
Med Intensiva (Engl Ed). 2021 Nov;45(8):485-500. doi: 10.1016/j.medine.2021.08.013. Epub 2021 Aug 24.
3
Myeloid phenotypes in severe COVID-19 predict secondary infection and mortality: a pilot study.
循环髓系来源的抑制性细胞可能是 COVID-19 未接种疫苗患者出院后随访的一个有用的生物标志物。
Front Immunol. 2023 Nov 14;14:1266659. doi: 10.3389/fimmu.2023.1266659. eCollection 2023.
4
Suppressive myeloid cells in SARS-CoV-2 and co-infection.抑制性髓系细胞在 SARS-CoV-2 和合并感染中的作用。
Front Immunol. 2023 Jul 20;14:1222911. doi: 10.3389/fimmu.2023.1222911. eCollection 2023.
5
Advances in the study of myeloid-derived suppressor cells in infectious lung diseases.感染性肺病中髓源性抑制细胞研究进展。
Front Immunol. 2023 Mar 29;14:1125737. doi: 10.3389/fimmu.2023.1125737. eCollection 2023.
6
Myeloid-derived suppressor cells and vaccination against pathogens.髓系来源的抑制细胞与病原体疫苗接种。
Front Cell Infect Microbiol. 2022 Sep 29;12:1003781. doi: 10.3389/fcimb.2022.1003781. eCollection 2022.
7
Myeloid-derived suppressor cells in COVID-19: A review.COVID-19 中的髓系来源抑制细胞:综述。
Clin Immunol. 2022 May;238:109024. doi: 10.1016/j.clim.2022.109024. Epub 2022 Apr 27.
重症 COVID-19 的髓系表型可预测继发感染和死亡率:一项初步研究。
Ann Intensive Care. 2021 Jul 14;11(1):111. doi: 10.1186/s13613-021-00896-4.
4
Myeloid-Derived Suppressor Cells as a Potential Biomarker and Therapeutic Target in COVID-19.髓系来源的抑制细胞作为 COVID-19 的潜在生物标志物和治疗靶点。
Front Immunol. 2021 Jun 18;12:697405. doi: 10.3389/fimmu.2021.697405. eCollection 2021.
5
Risk factors for mortality in critically ill patients with COVID-19: a multicenter retrospective case-control study.COVID-19 重症患者死亡的危险因素:一项多中心回顾性病例对照研究。
BMC Infect Dis. 2021 Jun 24;21(1):602. doi: 10.1186/s12879-021-06300-7.
6
Circulating myeloid-derived suppressor cells and regulatory T cells as immunological biomarkers in refractory/relapsed diffuse large B-cell lymphoma: translational results from the R2-GDP-GOTEL trial.循环髓系来源的抑制细胞和调节性 T 细胞作为复发/难治性弥漫性大 B 细胞淋巴瘤的免疫生物学标志物:R2-GDP-GOTEL 试验的转化研究结果。
J Immunother Cancer. 2021 Jun;9(6). doi: 10.1136/jitc-2020-002323.
7
The understanding of the immunopathology in COVID-19 infection.对 COVID-19 感染中免疫病理学的理解。
Scand J Clin Lab Invest. 2021 Jul;81(4):255-263. doi: 10.1080/00365513.2021.1892817. Epub 2021 May 25.
8
Immune Profile in Patients With COVID-19: Lymphocytes Exhaustion Markers in Relationship to Clinical Outcome.新型冠状病毒肺炎患者的免疫特征:淋巴细胞耗竭标志物与临床结局的关系
Front Cell Infect Microbiol. 2021 Apr 15;11:646688. doi: 10.3389/fcimb.2021.646688. eCollection 2021.
9
Decreased T Cell Levels in Critically Ill Coronavirus Patients: Single-Center, Prospective and Observational Study.危重症冠状病毒患者T细胞水平降低:单中心前瞻性观察研究
J Inflamm Res. 2021 Apr 9;14:1331-1340. doi: 10.2147/JIR.S303117. eCollection 2021.
10
Predictive factors of six-week mortality in critically ill patients with SARS-CoV-2: A multicenter prospective study.新型冠状病毒肺炎危重症患者6周死亡率的预测因素:一项多中心前瞻性研究。
Med Intensiva (Engl Ed). 2021 Mar 8;46(4):179-91. doi: 10.1016/j.medin.2021.02.013.