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Distinct CD8 T Cell Populations with Differential Exhaustion Profiles Associate with Secondary Complications in
Adam Klocperk1,2,3, David Friedmann4,5,6, Alexandra Emilia Schlaak7
1Center for Chronic Immunodeficiency (CCI), Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany. adam.klocperk@fnmotol.cz.
Insights
Common variable immunodeficiency (CVID) involves skewed CD8 T cells, showing exhaustion and activation. These changes correlate with CVID complications, offering insights into disease mechanisms and patient risk assessment.
Area of Science:
- Immunology
- Cellular Biology
Background:
- Common variable immunodeficiency (CVID) is a primary immunodeficiency with varied clinical outcomes.
- Understanding T cell dynamics is crucial for CVID pathogenesis.
Purpose of the Study:
- To analyze CD8 T cell homeostasis in CVID patients.
- To compare CD8 T cell profiles between infection-only CVID and CVID with dysregulation/autoimmunity.
Main Methods:
- Flow and mass cytometry on peripheral blood from 40 CVID patients and 17 healthy donors.
- Evaluation of CD8 T cell phenotypes, including exhaustion and activation markers.
Main Results:
- CVID patients exhibit CD8 T cell skewing: loss of naive, increased effector memory, and expanded exhausted populations.
- Activated, IL-10-producing CD8 T cells with immunoregulatory features were observed.
- Exhaustion markers correlate with interstitial lung disease and autoimmune cytopenias.
- Activation markers predict non-infectious diarrhea.
Conclusions:
- CD8 T cells in CVID patients display advanced differentiation, exhaustion, activation, and regulatory functions.
- CD8 T cell phenotyping may aid in CVID risk assessment.
- This study provides insights into T cell exhaustion and regulation in CVID.
Purpose:
Common variable immunodeficiency (CVID) is the most frequent symptomatic primary immunodeficiency, with heterogeneous clinical presentation. Our goal was to analyze CD8 T cell homeostasis in patients with infection only CVID, compared to those additionally affected by dysregulatory and autoimmune phenomena.
Methods:
We used flow and mass cytometry evaluation of peripheral blood of 40 patients with CVID and 17 healthy donors.
Results:
CD8 T cells are skewed in patients with CVID, with loss of naïve and increase of effector memory stages, expansion of cell clusters with high functional exhaustion scores, and a highly activated population of cells with immunoregulatory features, producing IL-10. These findings correlate to clinically widely used B cell-based EURO classification. Features of exhaustion, including loss of CD127 and CD28, and expression of TIGIT and PD-1 in CD8 T cells are strongly associated with interstitial lung disease and autoimmune cytopenias, whereas CD8 T cell activation with elevated HLA-DR and CD38 expression predict non-infectious diarrhea.
Conclusion:
We demonstrate features of advanced differentiation, exhaustion, activation, and immunoregulatory capabilities within CD8 T cells of CVID patients. Assessment of CD8 T cell phenotype may allow risk assessment of CVID patients and provide new insights into CVID pathogenesis, including a better understanding of mechanisms underlying T cell exhaustion and regulation.
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