1. Proinflammatory Potential of Cytomegalovirus Infection
- Author
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Hans W. Doerr, J. Cinatl, R. Kotchetkov, J.-U. Vogel, and Martin Scholz
- Subjects
Foscarnet ,Ganciclovir ,Chemokine ,virus diseases ,Biology ,medicine.disease_cause ,Molecular biology ,Proinflammatory cytokine ,chemistry.chemical_compound ,Infectious Diseases ,chemistry ,Antigen ,Downregulation and upregulation ,Virology ,medicine ,biology.protein ,Oxidative stress ,medicine.drug ,Cidofovir - Abstract
We observed the effects of antiviral therapy on CMV and/or oxidative-stress-induced stimulation of proinflammatory molecules including interleukin-8 (IL-8), melanoma growth stimulatory activity-α (GRO-α) and intercellular adhesion molecule 1 (ICAM-1) using human foreskin fibroblasts. Ganciclovir, foscarnet or cidofovir completely suppressed virus replication, as demonstrated by CMV late (L) antigen production. These drugs did not influence CMV immediate-early (IE) antigen expression and had no effects on CMV-induced cellular changes in IL-8, GRO-α and ICAM-1 levels. Phosphorothioate oligonucleotide (ISIS 2922) suppressed both CMV IE and L antigen by 99%. ISIS 2922 completely suppressed CMV-induced upregulation of both chemokines and ICAM-1. Induction of oxidative stress by H2O2 upregulated IL-8 expression. Oxidative stress and CMV infection showed synergistic effects on IL-8 expression. ISIS 2922 only partially inhibited the upregulation of IL-8 in infected cells treated with H2O2, whereas cotreatment with ISIS 2922 and antioxidants inhibited the upregulation almost completely. The results showed that inhibition of CMV IE expression alone or in combination with antioxidants is promising for the treatment of CMV disease.
- Published
- 1999
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