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评价不同感染阶段 COVID-19 患者外周血 CD3、CD4、CD8 T 细胞及 IgG、IgM 抗体水平。

Evaluation of the Levels of Peripheral CD3, CD4, and CD8 T Cells and IgG and IgM Antibodies in COVID-19 Patients at Different Stages of Infection.

机构信息

Research Center, King Fahad Medical City, Riyadh, Kingdom of Saudi Arabia.

Department of Basic Medical Sciences, College of Medicine, Dar Al-Uloom University, Riyadh, Kingdom of Saudi Arabia.

出版信息

Microbiol Spectr. 2022 Feb 23;10(1):e0084521. doi: 10.1128/spectrum.00845-21.

DOI:10.1128/spectrum.00845-21
PMID:35196808
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8865559/
Abstract

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection affects the stimulatory levels of cellular-mediated immunity, which plays an essential role in controlling SARS-CoV-2 infection. In fact, several studies have shown the association of lymphopenia with severe COVID-19 in patients. The aim of this study is to investigate the response of the immune system, including cell-mediated immunity and antibody production, during different stages of SARS-CoV-2 infection. Peripheral blood and serum samples were collected from patients with moderate infection, patients under medication (hospitalized), patients who had recovered, and healthy individuals ( = 80). Flow cytometry analysis was performed on peripheral blood samples to determine the cellular immunity profile of each patient. The data showed a significant reduction in the levels of CD3, CD4, and CD8 T cells and CD45 cells in the moderate and under-medication groups, suggesting lymphopenia in those patients. Also, enzyme-linked immunosorbent assay (ELISA) was conducted on the serum samples to measure the levels of antibodies, including IgM and IgG, in each patient. The results revealed a significant increase in the levels of IgM in the moderate infection and under-medication patients, thus indicating the production of IgM during the first week of infection. Furthermore, changes in the levels of IgG were significantly detected among recovered patients, indicating therefore a remarkable increase during the recovery stage of SARS-CoV-2 infection and thus a strong humoral-mediated immunity. In summary, the results of this study may help us to understand the main role of the cellular immune responses, including CD3, CD4, and CD8 T cells, against SARS-CoV-2 infection. This understanding might support the development of SARS-CoV-2 treatments and vaccines in the near future. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) emerged in late 2019 in China. This virus is a serious threat to people not only in China but also worldwide, where it has been detected in over 222 countries. It has been reported that ∼3.4% of SARS-CoV-2-infected patients have died. The significance of our study relies on the fact that an enzyme-linked immunosorbent assay and flow cytometry were used to measure the levels of antibodies and cellular immune response, respectively, from clinical samples of patients infected with SARS-CoV-2.

摘要

严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)感染会影响细胞介导的免疫刺激水平,而细胞介导的免疫在控制 SARS-CoV-2 感染方面起着至关重要的作用。事实上,多项研究表明,淋巴细胞减少与 COVID-19 患者的重症有关。本研究旨在探讨免疫系统对 SARS-CoV-2 感染不同阶段的反应,包括细胞介导的免疫和抗体产生。从中度感染的患者、接受药物治疗(住院)的患者、已康复的患者和健康个体(共 80 人)中采集外周血和血清样本。对患者外周血样本进行流式细胞术分析,以确定每位患者的细胞免疫特征。数据显示,中度感染和接受药物治疗的患者组的 CD3、CD4 和 CD8 T 细胞和 CD45 细胞水平显著降低,表明这些患者存在淋巴细胞减少症。此外,对血清样本进行酶联免疫吸附测定(ELISA)以测量每位患者的抗体水平,包括 IgM 和 IgG。结果表明,中度感染和接受药物治疗的患者的 IgM 水平显著升高,表明在感染的第一周内产生了 IgM。此外,在康复患者中还检测到 IgG 水平的显著变化,表明在 SARS-CoV-2 感染的康复阶段 IgG 显著增加,从而产生了强大的体液免疫。总之,本研究的结果可能有助于我们了解细胞免疫反应(包括 CD3、CD4 和 CD8 T 细胞)对 SARS-CoV-2 感染的主要作用。这一认识可能有助于在不久的将来开发 SARS-CoV-2 的治疗方法和疫苗。

严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)于 2019 年末在中国出现。该病毒不仅对中国,而且对全球范围内的人们都是一个严重的威胁,在全球超过 222 个国家都检测到了该病毒。据报道,约 3.4%的 SARS-CoV-2 感染患者死亡。本研究的意义在于使用酶联免疫吸附测定法和流式细胞术分别从 SARS-CoV-2 感染患者的临床样本中测量了抗体和细胞免疫反应的水平。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f74/8865559/c60b653c7290/spectrum.00845-21-f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f74/8865559/bf46daf029f1/spectrum.00845-21-f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f74/8865559/7b6cbae93907/spectrum.00845-21-f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f74/8865559/c60b653c7290/spectrum.00845-21-f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f74/8865559/bf46daf029f1/spectrum.00845-21-f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f74/8865559/7b6cbae93907/spectrum.00845-21-f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f74/8865559/c60b653c7290/spectrum.00845-21-f003.jpg

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2
Immunological memory to SARS-CoV-2 assessed for up to 8 months after infection.对感染后长达 8 个月的 SARS-CoV-2 进行免疫记忆评估。
Science. 2021 Feb 5;371(6529). doi: 10.1126/science.abf4063. Epub 2021 Jan 6.
3
Different Innate and Adaptive Immune Responses to SARS-CoV-2 Infection of Asymptomatic, Mild, and Severe Cases.
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Biomedicines. 2024 Jan 29;12(2):312. doi: 10.3390/biomedicines12020312.
4
Clinical features of omicron SARS-CoV-2 variants infection associated with co-infection and ICU-acquired infection in ICU patients.奥密克戎 SARS-CoV-2 变异株感染的临床特征与 ICU 患者合并感染和 ICU 获得性感染相关。
Front Public Health. 2024 Jan 5;11:1320340. doi: 10.3389/fpubh.2023.1320340. eCollection 2023.
5
Clinical characteristics associated with recurrent viral RNA positivity in patients within two weeks after recovering from the first SARS-CoV-2 infection.与首次感染 SARS-CoV-2 康复后两周内病毒 RNA 再次阳性相关的临床特征。
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6
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Clin Exp Med. 2023 Dec;23(8):5307-5313. doi: 10.1007/s10238-023-01176-0. Epub 2023 Aug 28.
7
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Cell. 2020 Nov 12;183(4):996-1012.e19. doi: 10.1016/j.cell.2020.09.038. Epub 2020 Sep 16.
7
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8
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Microb Pathog. 2020 Nov;148:104484. doi: 10.1016/j.micpath.2020.104484. Epub 2020 Sep 9.
9
Adaptive immune responses to SARS-CoV-2 infection in severe versus mild individuals.严重与轻度个体对 SARS-CoV-2 感染的适应性免疫反应。
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10
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