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Profiles of Peripheral Immune Cells of Uncomplicated COVID-19 Cases with Distinct Viral RNA Shedding Periods.
Putri, Denise Utami; Wang, Cheng-Hui; Tseng, Po-Chun; Lee, Wen-Sen; Chen, Fu-Lun; Kuo, Han-Pin; Lee, Chih-Hsin; Lin, Chiou-Feng.
  • Putri DU; Pulmonary Research Center, Wanfang Hospital, Taipei Medical University, Taipei 116, Taiwan.
  • Wang CH; Department of Laboratory Medicine, Wanfang Hospital, Taipei Medical University, Taipei 116, Taiwan.
  • Tseng PC; School of Medical Laboratory Science and Biotechnology, College of Medical Science and Technology, Taipei Medical University, Taipei 110, Taiwan.
  • Lee WS; Department of Microbiology and Immunology, School of Medicine, College of Medicine, Taipei Medical University, Taipei 110, Taiwan.
  • Chen FL; Core Laboratory of Immune Monitoring, Office of Research and Development, Taipei Medical University, Taipei 110, Taiwan.
  • Kuo HP; Divisions of Infectious Diseases, Department of Internal Medicine, Wanfang Hospital, Taipei Medical University, Taipei 116, Taiwan.
  • Lee CH; Divisions of Infectious Diseases, Department of Internal Medicine, Wanfang Hospital, Taipei Medical University, Taipei 116, Taiwan.
  • Lin CF; Divisions of Pulmonary Medicine, Department of Internal Medicine, School of Medicine, College of Medicine, Taipei Medical University, Taipei 110, Taiwan.
Viruses ; 13(3)2021 03 19.
Article in English | MEDLINE | ID: covidwho-1143617
ABSTRACT
The heterogeneity of immune response to COVID-19 has been reported to correlate with disease severity and prognosis. While so, how the immune response progress along the period of viral RNA-shedding (VRS), which determines the infectiousness of disease, is yet to be elucidated. We aim to exhaustively evaluate the peripheral immune cells to expose the interplay of the immune system in uncomplicated COVID-19 cases with different VRS periods and dynamic changes of the immune cell profile in the prolonged cases. We prospectively recruited four uncomplicated COVID-19 patients and four healthy controls (HCs) and evaluated the immune cell profile throughout the disease course. Peripheral blood mononuclear cells (PBMCs) were collected and submitted to a multi-panel flowcytometric assay. CD19+-B cells were upregulated, while CD4, CD8, and NK cells were downregulated in prolonged VRS patients. Additionally, the pro-inflammatory-Th1 population showed downregulation, followed by improvement along the disease course, while the immunoregulatory cells showed upregulation with subsequent decline. COVID-19 patients with longer VRS expressed an immune profile comparable to those with severe disease, although they remained clinically stable. Further studies of immune signature in a larger cohort are warranted.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: RNA, Viral / Leukocytes, Mononuclear / B-Lymphocytes / T-Lymphocytes / Virus Shedding / SARS-CoV-2 / COVID-19 Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study Limits: Adult / Female / Humans / Male / Middle aged / Young adult Language: English Year: 2021 Document Type: Article Affiliation country: V13030514

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Full text: Available Collection: International databases Database: MEDLINE Main subject: RNA, Viral / Leukocytes, Mononuclear / B-Lymphocytes / T-Lymphocytes / Virus Shedding / SARS-CoV-2 / COVID-19 Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study Limits: Adult / Female / Humans / Male / Middle aged / Young adult Language: English Year: 2021 Document Type: Article Affiliation country: V13030514