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(Circulation. 1996;94:2254-2259.)
© 1996 American Heart Association, Inc.

Articles

Antiviral Treatment With WIN 54 954 Reduces Mortality in Murine Coxsackievirus B3 Myocarditis

J. Fohlman, MD, PhD; K. Pauksen, MD, PhD; T. Hyypia, MD, PhD; G. Eggertsen, MD, PhD; A. Ehrnst, MD, PhD; N.G. Ilback, PhD; G. Friman, MD, PhD

the Department of Infectious Diseases, University Hospital, Uppsala, Sweden (J.F., K.P., N.G.I., G.F.); the Department of Virology, University of Turku, Finland (T.H.); Toxicology and Safety Assessment, Kabi Pharmacia AB, Helsingborg, Sweden (N.G.I.); the Division of Clinical Virology, Huddinge University Hospital, Karolinska Institute, Huddinge, Sweden (A.E.); and the Department of Medical Laboratory Sciences and Technology, Division of Clinical Chemistry, Huddinge Hospital, Huddinge, Sweden (G.E.).

Correspondence to Dr J. Fohlman, Department of Infectious Diseases, University Hospital, 751 85 Uppsala, Sweden.

Background Coxsackieviruses B (CBVs) are dominant causative agents in myocarditis and are associated with pathogenesis in some cases of dilated cardiomyopathy, a clinical entity with a poor survival without heart transplantation.

Methods and Results In vitro, the antiviral agent WIN 54 954 was shown to inhibit replication of CBV3 at a minimal inhibitory concentration value of 0.02 mg/L. Administration of WIN 54 954, 100 mg/kg BID PO, beginning on the day of infection resulted in complete protection from enteroviral mortality (P<.01). WIN 54 954 treatment did not abrogate the inflammatory reaction in the myocardium. No difference was found in the expression of surface lymphocyte subset markers. At 3 weeks, macrophages seemed to dominate the inflammatory reaction, regardless of treatment. There was no difference in CBV3 antibody titers, indicating that WIN 54 954 does not interfere with the development of protective immunity. Complement factors C3 and B were synthesized at a higher level during infection and correlated well with the degree of inflammatory reaction.

Conclusions The results show that WIN 54 954 is a potent antiviral agent with a highly significant effect on survival in CBV-induced myocarditis in the A/J mouse if treatment is started early. It is suggested that the reduction in mortality seen with WIN 54 954 administration is due to an inhibitory effect on virus replication in affected organs that does not interfere with cellular or humoral immunity.

Key Words: isoxazole • viruses • myocarditis • immunohistochemistry • cardiomyopathy

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