Using T-Cell Subsets to Better Characterize Immunoresiliency and Immunodeficiency in Patients with Recurrent
Justine Hung1, Bryan Vonasek2, Daniel Rosenberg1
1Department of Medicine, University of Wisconsin-Madison, Madison, WI 53706, USA.
Common Variable Immunodeficiency Disease (CVID) and other immunodeficiencies can be assessed using CD4/CD8 T cell ratios and Immune Health Grades. These biomarkers may help track disease severity and inform clinical decisions for patients with immune deficiencies.
Area of Science:
- Immunology
- Biomarker Discovery
- Clinical Assessment
Background:
- Common Variable Immunodeficiency Disease (CVID) and other immunodeficiencies present with subtle and variable clinical manifestations.
- Current biomarkers for quantifying immunodeficiency severity are not well understood.
- There is a need for reliable quantitative biomarkers to assess immunodeficiency severity.
Observation:
- The CD4/CD8 T cell ratio, particularly in the context of HIV literature, correlates with immunologic function and comorbidity.
- Immune Health Grades (IHG) offer a novel ranking system derived from diverse NIH cohorts.
- Most CVID patients exhibit not only antibody deficiencies but also abnormal CD4/CD8 ratios and cellular abnormalities.
Findings:
- Review of HIV literature indicates CD4/CD8 T cell ratios are more informative than CD4 counts alone for assessing immunologic status.
- Analysis of USIDNET data categorizes nine molecular immunodeficiencies, including CVID subtypes, based on CD4/CD8 ratios (low, normal, high).
- Two illustrative cases demonstrate how CD4/CD8 ratios and IHG can refine clinical assessment and management strategies.
Implications:
- Abnormalities in CD4/CD8 ratios and IHG may serve as clinically accessible biomarkers for grouping and monitoring immunodeficiencies.
- These biomarkers offer a quantifiable method to track disease progression or improvement in patients with immune deficiencies.
- Integrating CD4/CD8 ratios and IHG into clinical practice can enhance diagnostic accuracy and therapeutic guidance for immunodeficient patients.
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