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Published on: February 16, 2022
The laboratory tests and host immunity of COVID-19 patients with different severity of illness
Feng Wang1, Hongyan Hou1, Ying Luo1
1Department of Laboratory Medicine.
Insights
Investigating host immunity in COVID-19 patients reveals inconsistent T cell numbers and function. Hyperfunction of CD4+ and CD8+ T cells correlates with severe SARS-CoV-2 infection outcomes.
Area of Science:
- Immunology
- Virology
- Infectious Diseases
Background:
- The global outbreak of COVID-19 (caused by SARS-CoV-2) necessitates understanding host immune responses.
- The specific alterations in host immunity among COVID-19 patients with varying illness severity remain largely uncharacterized.
Purpose of the Study:
- To compare routine laboratory tests and host immune profiles in COVID-19 patients across different severity levels.
- To elucidate the relationship between immune cell dynamics and COVID-19 disease progression.
Main Methods:
- Analysis of routine laboratory tests and immune cell populations (CD4+, CD8+ T cells, B cells, Tregs) in 65 SARS-CoV-2-positive patients.
- Assessment of T cell activation markers (HLA-DR, CD45RO, CD28) and cytokine production (IFN-γ).
- Evaluation of regulatory T cell (Treg) percentages and immune cell activation markers.
Main Results:
- Severe and extremely severe COVID-19 cases showed elevated ferritin, lactate dehydrogenase, and D-dimer levels.
- Absolute counts of CD4+ T cells, CD8+ T cells, and B cells decreased with increasing illness severity.
- Increased T cell activation markers (HLA-DR, CD45RO) and IFN-γ production were observed in severe cases, alongside decreased CD28 expression and Treg percentages in extremely severe cases.
- Extremely severe patients exhibited increased IL-2R, IL-6, IL-10, and decreased DC and B cell activation.
Conclusions:
- COVID-19 patients exhibit variable T cell numbers and functions.
- Hyperfunction of CD4+ and CD8+ T cells is linked to the pathogenesis of extremely severe SARS-CoV-2 infection.
Abstract:
BACKGROUNDThe coronavirus disease 2019 (COVID-19), infected by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has caused a severe outbreak throughout the world. The host immunity of COVID-19 patients is unknown.METHODSThe routine laboratory tests and host immunity in COVID-19 patients with different severity of illness were compared after patient admission.RESULTSA total of 65 SARS-CoV-2-positive patients were classified as having mild (n = 30), severe (n = 20), and extremely severe (n = 15) illness. Many routine laboratory tests, such as ferritin, lactate dehydrogenase, and D-dimer, were increased in severe and extremely severe patients. The absolute numbers of CD4+ T cells, CD8+ T cells, and B cells were gradually decreased with increased severity of illness. The activation markers such as HLA-DR and CD45RO expressed on CD4+ and CD8+ T cells were increased in severe and extremely severe patients compared with mild patients. The costimulatory molecule CD28 had opposite results. The percentage of natural Tregs was decreased in extremely severe patients. The percentage of IFN-γ-producing CD8+ T cells was increased in both severe and extremely severe patients compared with mild patients. The percentage of IFN-γ-producing CD4+ T cells was increased in extremely severe patients. IL-2R, IL-6, and IL-10 were all increased in extremely severe patients. The activation of DC and B cells was decreased in extremely severe patients.CONCLUSIONThe number and function of T cells are inconsistent in COVID-19 patients. The hyperfunction of CD4+ and CD8+ T cells is associated with the pathogenesis of extremely severe SARS-CoV-2 infection.FUNDINGThis work was funded by the National Mega Project on Major Infectious Disease Prevention (2017ZX10103005-007) and the Fundamental Research Funds for the Central Universities (2019kfyRCPY098).
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