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Immune response in Dobrava-Belgrade virus infections
Katerina Tsergouli1, Anna Papa2
1Department of Microbiology, Medical School, Aristotle University of Thessaloniki, 54124, Thessaloniki, Greece.
Dobrava-Belgrade virus (DOBV) infection triggers distinct cytokine profiles in patients. Severe cases show elevated inflammatory markers, while non-severe cases exhibit a delayed immune response.
Area of Science:
- Immunology
- Virology
- Infectious Diseases
Background:
- Dobrava-Belgrade virus (DOBV) causes hemorrhagic fever with renal syndrome (HFRS).
- Hantaviral infections are characterized by increased vascular permeability and thrombocytopenia.
- Understanding the immune response is crucial for managing DOBV infections.
Purpose of the Study:
- To investigate the serum cytokine profiles in hospitalized Greek HFRS patients.
- To correlate cytokine levels with disease severity and clinical outcomes.
- To elucidate the dynamics of the immune response during DOBV infection.
Main Methods:
- Serum samples from 24 hospitalized Greek HFRS patients were analyzed.
- Levels of 27 cytokines were measured.
- Cytokine levels were compared between severe, non-severe, and fatal cases, as well as controls.
Main Results:
- Severe cases showed significantly higher levels of IL-1ra, IL-6, IL-8, IL-9, IL-10, GM-CSF, IP-10, MIP-1b, TNF-α, and VEGF compared to controls.
- Non-severe cases had significantly higher IL-13 and TNF-α levels.
- IP-10 was elevated, and RANTES decreased across all groups. VEGF correlated positively with disease severity. A strong, early immune response was observed in severe cases, while non-severe cases had a weaker, delayed response.
Conclusions:
- Distinct cytokine profiles are associated with DOBV infection severity.
- VEGF is a potential marker for disease severity.
- The timing and strength of the immune response, including Th1/Th2 balance, differ significantly among fatal, severe, and non-severe HFRS cases.
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