Soluble Tyro-3 and Axl may reflect the current activity and renal involvement in patients with microscopic

Tae Geom Lee1, Taejun Yoon2, Eunhee Ko2

  • 1Department of Medicine, Yonsei University College of Medicine, Seoul, Republic of Korea.

Abstract

Insights

Soluble Tyro-3 (sTyro-3) and sAxl show potential as biomarkers for microscopic polyangiitis (MPA) and granulomatosis with polyangiitis (GPA) activity. These markers correlate with disease severity and renal involvement in patients with ANCA-associated vasculitis (AAV).

Area of Science:

  • Immunology
  • Nephrology
  • Rheumatology

Background:

  • Microscopic polyangiitis (MPA) and granulomatosis with polyangiitis (GPA) are severe forms of antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV).
  • Accurate assessment of current disease activity and organ involvement is crucial for effective management of MPA and GPA.
  • Soluble forms of Tyro-3, Axl, and Mer receptor tyrosine kinases (sTyro-3, sAxl, sMer) are implicated in immune regulation and inflammation.

Purpose of the Study:

  • To investigate the potential of serum sTyro-3, sAxl, and sMer levels to reflect current disease activity in MPA and GPA patients.
  • To determine if these soluble biomarkers correlate with specific disease indices and organ involvement, particularly renal manifestations.

Main Methods:

  • Retrospective review of 76 patients diagnosed with MPA or GPA.
  • Measurement of serum sTyro-3, sAxl, and sMer concentrations at diagnosis.
  • Correlation analysis with established AAV activity indices: Birmingham Vasculitis Activity Score (BVAS), Five-Factor Score, SF-36, and Vasculitis Damage Index. High activity defined as highest BVAS tertile.

Main Results:

  • Serum concentrations of sTyro-3 and sAxl significantly correlated with BVAS and renal manifestation scores.
  • sTyro-3 and sAxl levels independently predicted BVAS scores (β=0.343 and β=0.310, respectively).
  • sTyro-3 and sAxl were independently associated with renal involvement in MPA and GPA (OR 1.003 and OR 1.055, respectively).

Conclusions:

  • Serum sTyro-3 and sAxl levels show potential as biomarkers reflecting current disease activity in MPA and GPA.
  • These markers are associated with both systemic disease activity (BVAS) and specific organ damage (renal involvement).
  • Further prospective studies are warranted to validate sTyro-3 and sAxl as reliable clinical tools for AAV management.

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