• 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

新型冠状病毒肺炎患者的免疫学评估:CD4+和 CD16+细胞可能预测疾病严重程度和预后。

Immunological evaluation of patients with 2019 novel coronavirus pneumonia: CD4+ and CD16+ cells may predict severity and prognosis.

机构信息

Science and Research branch, AJA University of Medical Sciences, Tehran, Iran.

Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

出版信息

PLoS One. 2022 Aug 5;17(8):e0268712. doi: 10.1371/journal.pone.0268712. eCollection 2022.

DOI:10.1371/journal.pone.0268712
PMID:35930526
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9355202/
Abstract

PURPOSE

Available but insufficient evidence shows that changes may occur in the immune system following coronavirus disease 2019 (COVID-19). The present study aimed at evaluating immunological changes in patients with severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) pneumonia compared with the control group.

METHOD

The present study was performed on 95 patients with COVID-19 (32 severe and 63 moderate cases) and 22 healthy controls. Relationship between immune cells, disease severity and lung involvement was assessed. Binary logistic regression and ROC curve tests were used for statistical analysis.

RESULTS

A significant decrease was observed in CD20+ cell counts of the patients. To differentiate patients from healthy individuals, the cutoff point for the CD4+ cell count was 688 /μL, sensitivity 0.96, and specificity 0.84. An increase in CD4+ cells reduces the odds of severe disease (odds ratio = 0.82, P = 0.047) and death (odds ratio = 0.74, P = 0.029). CD4+ cells play a pivotal role in the severity of lung involvement (P = 0.03). In addition to CD4+ cells, Fc gamma receptor III (FcγRIII) (CD16) also played a significant prognosis (odds ratio = 0.55, P = 0.047). In severe cases, C-reactive protein, Blood urea nitrogen, and Creatine phosphokinase levels, as well as neutrophil counts, were significantly higher than those of moderate ones whereas lymphocyte count in severe cases was lower than that of moderate ones.

CONCLUSION

The number of total T-cells and B-cells in patients with COVID-19 was lower than that of controls; however, their NK cells increased. FcγRIII and CD4+ cells are of great importance due to their association with COVID-19 prognosis.

摘要

目的

有证据表明,新冠肺炎(COVID-19)后,免疫系统可能会发生变化。本研究旨在评估严重急性呼吸综合征冠状病毒-2(SARS-CoV-2)肺炎患者与对照组之间的免疫变化。

方法

本研究纳入 95 例 COVID-19 患者(32 例重症,63 例轻症)和 22 例健康对照者。评估免疫细胞与疾病严重程度和肺部受累的关系。采用二项逻辑回归和 ROC 曲线检验进行统计学分析。

结果

患者的 CD20+细胞计数显著下降。为了将患者与健康个体区分开来,CD4+细胞计数的截断值为 688/μL,敏感性为 0.96,特异性为 0.84。CD4+细胞的增加降低了发生重症疾病的几率(比值比=0.82,P=0.047)和死亡的几率(比值比=0.74,P=0.029)。CD4+细胞在肺部受累的严重程度中起着关键作用(P=0.03)。除 CD4+细胞外,FcγRIII(CD16)也具有显著的预后意义(比值比=0.55,P=0.047)。在重症病例中,C 反应蛋白、血尿素氮、肌酸磷酸激酶水平以及中性粒细胞计数均显著高于轻症病例,而重症病例的淋巴细胞计数则低于轻症病例。

结论

COVID-19 患者的总 T 细胞和 B 细胞数量低于对照组,但其 NK 细胞增加。FcγRIII 和 CD4+细胞因其与 COVID-19 预后相关而非常重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/118d/9355202/24d411515666/pone.0268712.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/118d/9355202/dea245e964bf/pone.0268712.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/118d/9355202/24d411515666/pone.0268712.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/118d/9355202/dea245e964bf/pone.0268712.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/118d/9355202/24d411515666/pone.0268712.g002.jpg

相似文献

1
Immunological evaluation of patients with 2019 novel coronavirus pneumonia: CD4+ and CD16+ cells may predict severity and prognosis.新型冠状病毒肺炎患者的免疫学评估:CD4+和 CD16+细胞可能预测疾病严重程度和预后。
PLoS One. 2022 Aug 5;17(8):e0268712. doi: 10.1371/journal.pone.0268712. eCollection 2022.
2
Clinical and Immune Features of Hospitalized Pediatric Patients With Coronavirus Disease 2019 (COVID-19) in Wuhan, China.中国武汉 2019 年冠状病毒病(COVID-19)住院儿科患者的临床和免疫特征。
JAMA Netw Open. 2020 Jun 1;3(6):e2010895. doi: 10.1001/jamanetworkopen.2020.10895.
3
Clinical Characteristics and Immune Injury Mechanisms in 71 Patients with COVID-19.71 例 COVID-19 患者的临床特征和免疫损伤机制。
mSphere. 2020 Jul 15;5(4):e00362-20. doi: 10.1128/mSphere.00362-20.
4
[Value of interleukin-6 and CD4 T-lymphocytopenia in assessing the severity and prognosis of coronavirus disease 2019].[白细胞介素-6及CD4 T淋巴细胞减少在评估2019冠状病毒病严重程度及预后中的价值]
Zhonghua Wei Zhong Bing Ji Jiu Yi Xue. 2020 Oct;32(10):1165-1170. doi: 10.3760/cma.j.cn121430-20200521-00395.
5
Immune dysfunction following COVID-19, especially in severe patients.新冠病毒感染后免疫功能障碍,尤其是在重症患者中。
Sci Rep. 2020 Sep 28;10(1):15838. doi: 10.1038/s41598-020-72718-9.
6
The clinical course and its correlated immune status in COVID-19 pneumonia.新型冠状病毒肺炎的临床过程及其相关免疫状态。
J Clin Virol. 2020 Jun;127:104361. doi: 10.1016/j.jcv.2020.104361. Epub 2020 Apr 12.
7
Poor Survival in COVID-19 Associated with Lymphopenia and Higher Neutrophile-Lymphocyte Ratio.COVID-19 相关的低生存率与淋巴细胞减少和更高的中性粒细胞与淋巴细胞比值相关。
Isr Med Assoc J. 2021 Mar;23(3):153-159.
8
Baseline T-lymphocyte subset absolute counts can predict both outcome and severity in SARS-CoV-2 infected patients: a single center study.基线 T 淋巴细胞亚群绝对计数可预测 SARS-CoV-2 感染患者的结局和严重程度:一项单中心研究。
Sci Rep. 2021 Jun 17;11(1):12762. doi: 10.1038/s41598-021-90983-0.
9
Lymphocyte Subset Alteration and Monocyte CD4 Expression Reduction in Patients with Severe COVID-19.严重 COVID-19 患者的淋巴细胞亚群改变和单核细胞 CD4 表达减少。
Viral Immunol. 2021 Jun;34(5):342-351. doi: 10.1089/vim.2020.0166. Epub 2020 Nov 23.
10
Clinical characteristics and peripheral immunocyte subsets alteration of 85 COVID-19 deaths.COVID-19 死亡 85 例的临床特征及外周免疫细胞亚群改变。
Aging (Albany NY). 2021 Mar 12;13(5):6289-6297. doi: 10.18632/aging.202819.

引用本文的文献

1
Coronary artery calcification: Effects on severity and survival in patients with COVID-19.冠状动脉钙化:对新型冠状病毒肺炎患者病情严重程度和生存情况的影响
J Res Med Sci. 2022 Dec 23;27:89. doi: 10.4103/jrms.jrms_584_21. eCollection 2022.

本文引用的文献

1
Autoantibodies in moderate and critical cases of COVID-19.新冠病毒肺炎中重度和危重症病例中的自身抗体。
Clin Transl Sci. 2021 Sep;14(5):1625-1626. doi: 10.1111/cts.13036. Epub 2021 May 2.
2
Antinuclear antibodies in COVID 19.新型冠状病毒肺炎中的抗核抗体
Clin Transl Sci. 2021 Sep;14(5):1627-1628. doi: 10.1111/cts.13026. Epub 2021 May 1.
3
Understanding the role of neutrophils in acute respiratory distress syndrome.了解中性粒细胞在急性呼吸窘迫综合征中的作用。
Biomed J. 2021 Aug;44(4):439-446. doi: 10.1016/j.bj.2020.09.001. Epub 2020 Sep 10.
4
COVID-19 and Immunological Dysregulation: Can Autoantibodies be Useful?COVID-19 与免疫失调:自身抗体是否有用?
Clin Transl Sci. 2021 Mar;14(2):502-508. doi: 10.1111/cts.12908. Epub 2021 Jan 20.
5
Comorbidity and its Impact on Patients with COVID-19.合并症及其对COVID-19患者的影响。
SN Compr Clin Med. 2020;2(8):1069-1076. doi: 10.1007/s42399-020-00363-4. Epub 2020 Jun 25.
6
An immunotherapeutic method for COVID-19 patients: a soluble ACE2-Anti-CD16 VHH to block SARS-CoV-2 Spike protein.用于 COVID-19 患者的免疫治疗方法:一种可溶性 ACE2-Anti-CD16 VHH 以阻断 SARS-CoV-2 刺突蛋白。
Hum Vaccin Immunother. 2021 Jan 2;17(1):92-97. doi: 10.1080/21645515.2020.1787066. Epub 2020 Jul 14.
7
Immunology of COVID-19: Current State of the Science.COVID-19 的免疫学:科学现状。
Immunity. 2020 Jun 16;52(6):910-941. doi: 10.1016/j.immuni.2020.05.002. Epub 2020 May 6.
8
Targets of T Cell Responses to SARS-CoV-2 Coronavirus in Humans with COVID-19 Disease and Unexposed Individuals.COVID-19 疾病患者和未接触者体内针对 SARS-CoV-2 冠状病毒的 T 细胞反应的靶标。
Cell. 2020 Jun 25;181(7):1489-1501.e15. doi: 10.1016/j.cell.2020.05.015. Epub 2020 May 20.
9
COVID-19-associated immune thrombocytopenia.新型冠状病毒肺炎相关免疫性血小板减少症
Br J Haematol. 2020 Jul;190(2):e61-e64. doi: 10.1111/bjh.16850. Epub 2020 Jun 8.
10
Detection of SARS-CoV-2-Specific Humoral and Cellular Immunity in COVID-19 Convalescent Individuals.新型冠状病毒感染恢复期个体中 SARS-CoV-2 特异性体液和细胞免疫的检测。
Immunity. 2020 Jun 16;52(6):971-977.e3. doi: 10.1016/j.immuni.2020.04.023. Epub 2020 May 3.