Association Between Serum Soluble Programmed Death Ligand 1 Levels and Disease Severity in Patients with

Ayten Yanık1, Ömer Karaşahin1, Rukiye İnan Sarıkaya2

  • 1Department of Infectious Diseases and Clinical Microbiology, Erzurum City Hospital, Erzurum, Turkey.

Insights

Elevated soluble programmed death-ligand 1 (sPD-L1) levels indicate greater severity in Crimean-Congo hemorrhagic fever (CCHF) patients. This biomarker shows strong potential for predicting CCHF disease progression and patient outcomes.

Area of Science:

  • Virology
  • Immunology
  • Clinical Medicine

Background:

  • Crimean-Congo hemorrhagic fever (CCHF) is a severe viral illness associated with coagulopathy and multiorgan failure.
  • The programmed cell death protein 1/programmed death ligand 1 (PD-L1) pathway modulates inflammation, but its role in CCHF, particularly soluble PD-L1 (sPD-L1), is unclear.

Purpose of the Study:

  • To quantify serum sPD-L1 levels in CCHF patients.
  • To assess the association between sPD-L1 levels and CCHF disease severity and prognosis.

Main Methods:

  • A prospective study involving 60 confirmed CCHF adult patients and 30 healthy controls.
  • Serum sPD-L1 levels were measured on admission, alongside routine laboratory tests and clinical data.
  • Disease severity was assessed using the Severity Scoring Index, with statistical analyses including correlation and receiver operating characteristic (ROC) curves.

Main Results:

  • Moderate-to-severe CCHF cases exhibited more frequent neurological symptoms, fever, diarrhea, and bleeding compared to mild cases.
  • Patients with moderate-to-severe CCHF had significantly lower platelet and fibrinogen levels and elevated liver enzymes, LDH, INR, and aPTT.
  • Serum sPD-L1 levels were comparable in healthy controls and mild CCHF cases but significantly higher in moderate-to-severe CCHF cases (AUC: 0.901).

Conclusions:

  • Elevated serum sPD-L1 levels are strongly correlated with increased disease severity in CCHF.
  • sPD-L1 demonstrates significant potential as a prognostic biomarker for CCHF, warranting further investigation in larger cohorts.

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