Lupus & antiphospholipid syndrome

Single-cell transcriptome analyses reveal disturbed decidual homoeostasis in obstetric antiphospholipid syndrome

Ann Rheum DisPublished Mechanistic study

Authors' conclusion

This study provided a comprehensive decidual cell landscape and identified aberrant decidual microenvironment in OAPS

Study context

Population
First-trimester decidua from patients with obstetric APS and healthy controlsplus larger validation cohort
Participants
5 vs 5
Comparison
Obstetric APS vs healthy controls
  • Obstetric antiphospholipid syndrome (OAPS)n = 5
  • Healthy controls (HCs)n = 5reference
Outcome
Cellular compositions and molecular features of decidual cells (single-cell RNA sequencing (scRNA-seq))
Follow-up
First trimester
Methodological detailssingle-cell RNA sequencing, validation with flow cytometry, immunohistochemical staining and immunofluorescence in a larger cohort
  • Single-cell RNA sequencing
  • Validation with flow cytometry, immunohistochemical staining and immunofluorescence in a larger cohort

Main finding

As reported in the abstract

Decidual cell composition and molecular features
  • Higher ratio of macrophages but lower ratio of decidual natural killer (dNK) cells in OAPS vs HCs
  • Vascular endothelial cells shrank in OAPS decidua, with upregulated chemokine expression and conspicuous responses to IFN-γ and TNF-α
  • OAPS macrophages: stronger phagocytosis, complement activation signals, more reliance on glycolysis
  • OAPS dNK cells more activated, with enhanced cytotoxicity and IFN-γ production; downregulated granules possibly associated with suppressed glycolysis
  • Stromal cells in prosenescent state with weakened immune surveillance for senescent cells in OAPS
  • Altered cellular interactions among immune cells and between immune and non-immune cells, especially via chemokines, IFN-γ and TNF-α

Original publication

Single-cell transcriptome analyses reveal disturbed decidual homoeostasis in obstetric antiphospholipid syndrome. Ann Rheum Dis. Published 11 April 2024. doi:10.1136/ard-2023-224930

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