1. Role of prostaglandin e2 on defective interferon-γ production during type b acute viral hepatitis
- Author
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Mazzetti M, Giovanni Gasbarrini, Giuseppe Francesco Stefanini, Mario Baraldini, Patrizia Pasini, Pietro Andreone, Gabriella Verucchi, and Carmela Cursaro
- Subjects
Adult ,Male ,medicine.medical_specialty ,Adolescent ,Clinical Biochemistry ,Biology ,medicine.disease_cause ,Peripheral blood mononuclear cell ,Dinoprostone ,Interferon-gamma ,chemistry.chemical_compound ,Interferon ,Internal medicine ,medicine ,Humans ,Prostaglandin E2 ,Cells, Cultured ,Hepatitis B virus ,Hematology ,Interferon-gamma production ,Prostanoid ,Middle Aged ,Hepatitis B ,medicine.disease ,chemistry ,Acute Disease ,Immunology ,Leukocytes, Mononuclear ,Female ,lipids (amino acids, peptides, and proteins) ,Viral hepatitis ,medicine.drug - Abstract
Interferon-gamma (IFN-gamma) and prostaglandin E2 (PGE2) production was evaluated in cultured peripheral blood mononuclear cells taken from patients with type B acute viral hepatitis at the onset of symptoms, at 1st and 2nd week of disease, and from healthy controls. Concanavalin A-stimulated cells cultured for 24, 48 and 72h showed significantly higher IFN-gamma levels compared to basal release in both groups, whereas no statistically significant differences were found in most experimental conditions as regard PGE2 synthesis. No differences were found in IFN-gamma production by comparing patients with acute viral hepatitis to the control group, whereas PGE2 was significantly increased during the disease. IFN-gamma and PGE2 levels did not show any significant change in acute viral hepatitis during the follow-up. A statistically significant correlation was found only in control group between IFN-gamma and PGE2 levels in unstimulated cultures. PGE2 seems to play a central role in regulating interferon production during viral infection. This may suggest a new therapeutic approach in viral hepatitis utilizing a combination of interferon and prostanoid inhibitory substances, above all in patients who do not respond to interferon therapy alone.
- Published
- 1991