Immune Response Profiling in COVID-19 Patients

Summary

Immune response profiling in COVID-19 patients encompasses systematic analyses of both innate and adaptive components, integrating cellular, humoral and molecular measurements. Quantification of lymphocyte subsets (CD4+ and CD8+ T cells, B cells, natural killer cells), multiplex cytokine and chemokine panels, and high-resolution transcriptomic or proteomic assays have revealed characteristic patterns of lymphopaenia, hyperinflammatory cytokine release (“cytokine storm”) and T cell exhaustion. Longitudinal studies demonstrate persistent remodelling of naïve and memory T cell pools beyond acute illness, while multi-parameter signatures have identified prognostic biomarkers to stratify patient risk and guide immunomodulatory therapy. Advances in single-cell sequencing and integrated omics have illuminated mechanisms of viral pathogenesis, informed vaccine optimisation and underpinned personalised management strategies worldwide.

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Immune Response Profiling in COVID-19 Patients publication trend

The graph below shows the total number of articles in immune response profiling in covid-19 patients across all publications each year (not limited to Nature Index journals).

Technical terms

CD8+ T cell: A subset of cytotoxic lymphocytes that recognise infected cells via the major histocompatibility complex and mediate targeted cell killing.

Cytokine storm: An excessive and dysregulated release of pro-inflammatory cytokines leading to systemic inflammation and tissue damage.

Naïve T cell: A mature T lymphocyte that has not yet encountered its specific antigen and circulates awaiting activation.

Lymphopaenia: A reduction in the absolute number of lymphocytes in peripheral blood, often correlating with impaired immune competence.

Biomarker: A measurable biological indicator used to predict clinical outcomes, monitor disease progression or guide therapeutic decisions.

References

  1. Immunophenotyping characteristics and outcome of COVID‐19 patients: peripheral blood CD8+T cell as a prognostic biomarker for patients with Nirmatrelvir. Frontiers in Immunology (2023).
  2. Inflammatory Response in COVID-19 Depending on the Severity of the Disease and the Vaccination Status. International Journal of Molecular Sciences (2023).
  3. Prospective and Longitudinal Analysis of Lymphocyte Subpopulations in SARS-CoV-2 Positive and Negative Pneumonia: Potential Role of Decreased Naïve CD8+ in COVID-19 Patients. Viruses (2024).

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