NKG2A Expression among CD8 Cells Is Associated with COVID-19 Progression in Hypertensive Patients: Insights from the
Renata Moll-Bernardes1, Sérgio C Fortier1,2, Andréa S Sousa1,3
1D'Or Institute for Research and Education, Rio de Janeiro 22281-100, Brazil.
Insights
Hypertension patients with COVID-19 and higher CD8+ NKG2A MFI on admission faced severe disease progression. This immune marker, along with clinical factors, indicates a high risk, suggesting T cell exhaustion in severe cases.
Area of Science:
- Immunology
- Virology
- Cardiology
Background:
- Cardiovascular comorbidities and immune dysregulation are linked to severe COVID-19.
- Hypertension is a significant risk factor for adverse COVID-19 outcomes.
- Understanding immune cell profiles in hypertensive COVID-19 patients is crucial for predicting disease severity.
Purpose of the Study:
- To investigate the immune cell profile in hospitalized hypertensive patients with COVID-19.
- To identify immune cell subsets associated with progression to severe COVID-19.
- To explore the relationship between immune markers and clinical variables in predicting disease severity.
Main Methods:
- A logistic regression model was used to analyze data from 156 hospitalized hypertensive patients with COVID-19.
- Clinical variables and immune cell subsets were assessed on admission.
- The primary outcome was progression to severe COVID-19 disease.
Main Results:
- Obesity, diabetes, low oxygen saturation, lung CT findings, elevated C-reactive protein, and altered lymphocyte counts (total, CD4+, CD8+, CD4/CD8 ratio) were associated with severe COVID-19.
- Increased CD8+ NKG2A MFI (Mean Fluorescence Intensity) on admission was significantly linked to a higher risk of progression.
- CD8+ HLA-DR MFI also showed association with disease progression.
Conclusions:
- Increased CD8+ NKG2A MFI at hospital admission is a key indicator of severe COVID-19 progression risk in hypertensive patients.
- Findings support the hypothesis of T cell exhaustion in severe COVID-19, evidenced by NKG2A expression.
- These insights may offer potential therapeutic targets for mitigating severe acute respiratory syndrome coronavirus 2 infection.
Abstract:
Cardiovascular comorbidities and immune-response dysregulation are associated with COVID-19 severity. We aimed to explore the key immune cell profile and understand its association with disease progression in 156 patients with hypertension that were hospitalized due to COVID-19. The primary outcome was progression to severe disease. The probability of progression to severe disease was estimated using a logistic regression model that included clinical variables and immune cell subsets associated with the primary outcome. Obesity; diabetes; oxygen saturation; lung involvement on computed tomography (CT) examination; the C-reactive protein concentration; total lymphocyte count; proportions of CD4+ and CD8+ T cells; CD4/CD8 ratio; CD8+ HLA-DR MFI; and CD8+ NKG2A MFI on admission were all associated with progression to severe COVID-19. This study demonstrated that increased CD8+ NKG2A MFI at hospital admission, in combination with some clinical variables, is associated with a high risk of COVID-19 progression in hypertensive patients. These findings reinforce the hypothesis of the functional exhaustion of T cells with the increased expression of NKG2A in patients with severe COVID-19, elucidating how severe acute respiratory syndrome coronavirus 2 infection may break down the innate antiviral immune response at an early stage of the disease, with future potential therapeutic implications.
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