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The immune inflammation factors associated with disease severity and poor prognosis in patients with COVID-19: A
Yanli Kang1, Shifa Lu2, Ruifang Zhong1
1Department of Clinical Laboratory, Fujian Provincial Hospital, Shengli Clinical Medical College of Fujian Medical University, Fuzhou, China.
Insights
Severe COVID-19 involves immune dysregulation, with increased IL-6, IL-8, IL-10, and IFN-γ. Lower CD8+ T-cell and NK cell counts predict poor outcomes, highlighting their potential as biomarkers for disease progression.
Area of Science:
- Immunology
- Virology
- Clinical Medicine
Background:
- Coronavirus disease 2019 (COVID-19) is linked to immune system dysfunction and cytokine storms.
- Understanding peripheral immune responses is crucial for COVID-19 pathogenesis and prognosis.
Purpose of the Study:
- To analyze immune response characteristics in COVID-19 patients.
- To identify immunological markers for disease severity and progression.
Main Methods:
- Retrospective analysis of immunoglobulins, complement, lymphocyte subsets (CD3+, CD4+, CD8+, NK, CD19+, CD45+), and cytokines (IL-2, IL-4, IL-5, IL-6, IL-8, IL-10, IL-17, IL-12p, IL-1β, TNF-α, IFN-α, IFN-γ) in 513 COVID-19 patients.
- Patients categorized into mild/moderate, severe survivors, and severe non-survivors.
Main Results:
- Severe COVID-19 showed elevated IL-6, IL-8, IL-10, and IFN-γ with decreased CD45+, CD3+, CD4+, CD8+, CD19+, and NK cells compared to non-severe cases.
- Non-survivors had higher IL-6, IL-8, IL-10 and lower C3, CD45+, CD3+, CD4+, CD8+, and NK cells than severe survivors.
- Age, IL-8, IL-10, CD8+ cells, and NK cells were independent risk factors for COVID-19 severity.
Conclusions:
- Immune factors like IL-6, IL-8, IL-10, CD8+ T-cells, and NK cells are associated with COVID-19 severity and progression.
- These immune markers can potentially be used for monitoring and predicting COVID-19 outcomes.
- Tumor presence, older age, high IL-8/IL-10, and low CD8+/NK cell levels correlate with shorter survival times.
Abstract:
Coronavirus disease 2019 (COVID-19) is associated with immune dysregulation and cytokine storm. It is essential to explore the immune response characteristics of peripheral circulation in COVID-19 patients to reveal pathogenesis and predict disease progression. In this study, the levels of total immunoglobulins (IgG, IgM, IgA), complement (C3, C4),lymphocyte subsets (CD3+ cell,CD4+ cell,CD8+ cell, NK cell, CD19+ cell and CD45+ cell) and cytokines (IL-2, IL-4, IL-5, IL-6, IL-8, IL-10, IL-17, IL-12p, IL-1β, TNF-α, IFN-α and IFN-γ) were retrospectively analyzed in COVID-19 patients. A total of 513 patients were enrolled in this study, cases were distributed according to clinical status as mild or moderate (n = 212), severe survivors (n = 197) and severe non-survivors (n = 104). IL-6, IL-8, IL-10 and IFN-γ were increased in severe patients compared with non-severe patients, despite decreased CD45+ cell, CD3+ cell, CD4+ cell, CD8+ cell, CD19+ cell, and NK cell. Compared with severe survivors, the levels of L-6, IL-8 and IL-10 in non-survivors increased significantly, and levels of C3, CD45+ cell, CD3+ cell,CD4+ cell,CD8+ cell, and NK cell decreased. Moreover, age, IL-8, IL-10, CD8+cells and NK cell were independent risk factors for the severity of COVID-19. Multivariable regression showed increasing odds ratio of in-hospital death associated with tumor, older age, higher IL-8 level, and decreasing odds ratio of in-hospital death associated with increased levels of CD8+cell and NK cell. Finally, patients with tumor, or high IL-6 or high IL-10 expression and lower CD8+ or lower NK levels exhibited a significantly shorter survival time. In conclusion, our study provides findings of the immunological characteristics associated with disease severity to predict the progression of COVID-19. The immune inflammation factors, such as IL-6, IL-8, IL-10, CD8+ cell and NK cell, could serve as excellent biomarkers for monitoring or predicting COVID-19 progression therapeutic to COVID-19 patients.
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