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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.
Abstract:
Crimean-Congo hemorrhagic fever (CCHF) is a severe viral infection that may lead to coagulopathy and multiorgan failure. Although the programmed cell death protein 1/programmed death ligand 1 (PD-L1) immune checkpoint pathway regulates excessive inflammation, the clinical significance of circulating soluble PD-L1 (sPD-L1) in CCHF is not well defined. The aim for the present study was to measure serum sPD-L1 levels in patients with CCHF and evaluate their association with disease severity and prognosis. This prospective study included 60 adults with confirmed CCHF and 30 healthy controls. Disease severity was classified using the Severity Scoring Index. Serum collected on admission was analyzed for sPD-L1, and routine laboratory values were recorded. Clinical and laboratory differences between severity groups were examined, and correlation and receiver operating characteristic analyses were performed. Neurological symptoms, fever, diarrhea, and bleeding were more common in moderate-to-severe cases. These patients had significantly lower platelet and fibrinogen levels and higher alanine aminotransferase, aspartate aminotransferase, lactate dehydrogenase, international normalized ratio, and activated partial thromboplastin time values. Soluble PD-L1 levels were similar in healthy controls and mild cases but were markedly elevated in moderate-to-severe cases. Soluble PD-L1 accounted for more than half of the variation in severity scores (R2 = 0.556). Receiver operating characteristic analysis revealed strong discriminatory ability (area under the curve: 0.901), with a cutoff of 10.91 ng/mL yielding 96.7% sensitivity and 80% specificity. In conclusion, elevated sPD-L1 levels are closely associated with disease severity in CCHF. Soluble PD-L1 may have prognostic value, although this association should be confirmed in larger studies.
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