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.

JCI Insight
|April 24, 2020
PubMed

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.

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