J Gen Virol Try Microbiology Online
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Gen Virol 64 (1983), 2317-2321; DOI 10.1099/0022-1317-64-10-2317
© 1983 Society for General Microbiology

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Fish, E. N.
Right arrow Articles by Stebbing, N.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Fish, E. N.
Right arrow Articles by Stebbing, N.
Agricola
Right arrow Articles by Fish, E. N.
Right arrow Articles by Stebbing, N.

Antiviral Activities of Cloned Human Leukocyte Interferons against Herpes Simplex Virus Type 2 Infections of Mice

E. N. Fish, K. Banerjee and N. Stebbing1

Division of Infectious Diseases, Research Institute Hospital for Sick Children, 555 University Avenue, Toronto, Ontario M5G 1X8, Canada
and1 Applied Molecular Genetics, Inc., 1900 Oak Terrace Lane, Thousand Oaks, California 91320, U.S.A.

Human {alpha}-interferons (IFN-{alpha}s) made in bacteria were examined for antiviral activity against herpes simplex virus type 2 (HSV-2) infections of mouse L-cells in vitro, and acute cervicovaginal and lethal systemic HSV-2 infections of BALB/c mice. The recombinant DNA-derived hybrid interferon IFN-{alpha}AD(Bgl) showed pronounced antiviral activity in vitro, exceeding the activity of either of the parental subtypes IFN-{alpha}A and IFN-{alpha}D and that of the other hybrids IFN-{alpha}AD(Pvu). A combination of topical and systemic treatments with IFN-{alpha}A and IFN-{alpha}AD(Bgl) failed to protect mice from subsequent challenge with an acute cervicovaginal infection of HSV-2. Protection from lethal systemic HSV-2 infection in mice was observed when IFN-{alpha}AD(Bgl) and IFN-{alpha}AD(Pvu) were administered systemically, whereas IFN-{alpha}A failed to confer protection. These results suggest that for protection against infection with HSV-2, the routes of introduction of the virus and of the interferon influence the host response to interferon therapy.

Keywords: interferon (HuIFN-{alpha}), cloned IFN, HSV-2, antiviral activities

Received 8 March 1983; accepted 10 June 1983.





HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL MICROBIOLOGY J GEN VIROL
J MED MICROBIOL ALL SGM JOURNALS
Copyright © 1983 by the Society for General Microbiology.