Different T cell related immunological profiles in COVID-19 patients compared to healthy controls

Armin Mahmoud Salehi Khesht1, Vahid Karpisheh2, Balsam Qubais Saeed3

  • 1Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran; Department of Biochemistry, Faculty of Materials Engineering, Islamic Azad University, Najafabad Branch, Najafabad, Iran.

Insights

Severe COVID-19 disease alters T lymphocyte balance, increasing inflammatory Th1/Th17 cells while decreasing regulatory Treg cells and their function. This impacts cellular immunity and disease pathogenesis.

Area of Science:

  • Immunology
  • Cellular Immunity
  • COVID-19 Pathogenesis

Background:

  • Cellular immunity, particularly T lymphocytes, is crucial in pathological conditions and COVID-19 pathogenesis.
  • Understanding T lymphocyte frequency and function in SARS-CoV-2 patients is vital for disease comprehension.

Purpose of the Study:

  • To examine the frequency and function of T lymphocytes in SARS-CoV-2 patients across different disease severities compared to healthy individuals.
  • To investigate the impact of COVID-19 severity on T cell cytokine secretion and regulatory T cell (Treg) inhibitory activity.

Main Methods:

  • Comparative analysis of T lymphocyte populations (Th1, Th2, Th17, Treg) in asymptomatic recovered, non-ICU hospitalized, ICU hospitalized COVID-19 patients, and normal subjects.
  • Assessment of cytokine secretion (IL-17, IFN-γ, IL-10, IL-4) and Treg cell inhibitory function post-purification.

Main Results:

  • Severe COVID-19 (ICU patients) showed increased Th1 and Th17 cells, alongside decreased Th2 and Treg cells.
  • Elevated IL-17 and IFN-γ secretion, with reduced IL-10 and IL-4, was observed in severe cases.
  • Treg cell inhibitory activity was significantly diminished in severe COVID-19 patients.

Conclusions:

  • Severe COVID-19 is characterized by an amplified inflammatory response (Th1/Th17) and a weakened anti-inflammatory/regulatory response (Th2/Treg).
  • The imbalance in T cell subsets and function contributes to the pathogenesis of severe SARS-CoV-2 infection.

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