Cytotoxic CD161 - CD8 + T EMRA cells contribute to the pathogenesis of systemic lupus erythematosus
Systemic lupus erythematosus (SLE) is a prototypical autoimmune disease affecting multiple organs and tissues with high cellular heterogeneity. CD8 T cell activity is involved in the SLE pathogenesis. However, the cellular heterogeneity and the underlying mechanisms of CD8 T cells in SLE remain to b...
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Veröffentlicht in: | EBioMedicine 2023-04, Vol.90, p.104507 |
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Zusammenfassung: | Systemic lupus erythematosus (SLE) is a prototypical autoimmune disease affecting multiple organs and tissues with high cellular heterogeneity. CD8
T cell activity is involved in the SLE pathogenesis. However, the cellular heterogeneity and the underlying mechanisms of CD8
T cells in SLE remain to be identified.
Single-cell RNA sequencing (scRNA-seq) of PBMCs from a SLE family pedigree (including 3 HCs and 2 SLE patients) was performed to identify the SLE-associated CD8
T cell subsets. Flow cytometry analysis of a SLE cohort (including 23 HCs and 33 SLE patients), qPCR analysis of another SLE cohort (including 30 HCs and 25 SLE patients) and public scRNA-seq datasets of autoimmune diseases were employed to validate the finding. Whole-exome sequencing (WES) of this SLE family pedigree was used to investigate the genetic basis in dysregulation of CD8
T cell subsets identified in this study. Co-culture experiments were performed to analyze the activity of CD8
T cells.
We elucidated the cellular heterogeneity of SLE and identified a new highly cytotoxic CD8
T cell subset, CD161
CD8
T
cell subpopulation, which was remarkably increased in SLE patients. Meanwhile, we discovered a close correlation between mutation of DTHD1 and the abnormal accumulation of CD161
CD8
T
cells in SLE. DTHD1 interacted with MYD88 to suppress its activity in T cells and DTHD1 mutation promoted MYD88-dependent pathway and subsequently increased the proliferation and cytotoxicity of CD161
CD8
T
cells. Furthermore, the differentially expressed genes in CD161
CD8
T
cells displayed a strong out-of-sample prediction for case-control status of SLE.
This study identified DTHD1-associated expansion of CD161
CD8
T
cell subpopulation is critical for SLE. Our study highlights genetic association and cellular heterogeneity of SLE pathogenesis and provides a mechanistical insight into the diagnosis and treatment of SLE.
Stated in the Acknowledgements section of the manuscript. |
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ISSN: | 2352-3964 |