Suppression of Recurrent Genital Herpes Simplex Virus Infection with Recombinant$α_2$Interferon
This double-blind, placebo-controlled study evaluated the efficacy and safety of sc administered recombinant α₂ interferon (IFN-α₂) in the suppression of frequently recurrent genital herpes simplex virus (HSV) infection. Seventy-six otherwise healthy subjects who had eight or more recurrences during...
Saved in:
Published in | The Journal of infectious diseases Vol. 154; no. 3; pp. 437 - 442 |
---|---|
Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
University of Chicago Press
01.09.1986
|
Subjects | |
Online Access | Get full text |
ISSN | 0022-1899 |
DOI | 10.1093/infdis/154.3.437 |
Cover
Summary: | This double-blind, placebo-controlled study evaluated the efficacy and safety of sc administered recombinant α₂ interferon (IFN-α₂) in the suppression of frequently recurrent genital herpes simplex virus (HSV) infection. Seventy-six otherwise healthy subjects who had eight or more recurrences during the preceding year received 1 x$10^6$IU of IFN-α₂, 3 x$10^6$IU of IFN-α₂, or placebo three times per week for 12 weeks. Recipients of the higher dose of IFN-α₂, had fewer outbreaks during the study (2 vs. 3), a shorter period of viral shedding (2 vs. 4 days), less itching (1 vs. 3 days), and a faster healing time (6 vs. 8 days). The lower dose of IFN-α₂ was not effective. Significant side effects (fever, malaise, myalgia, fatigue, and arthralgia) occurred after the first injection of 3 x$10^6$IU of IFN-α₂ in 91% of the subjects, but subsequent injections produced only mild and intermittent side effects that were well tolerated. Mild leukopenia was noted in subjects treated with IFN-α₂. Treatment with IFN-α₂ resulted in moderate suppression and decreased duration of recurrent genital HSV infection in patients with frequent recurrences. |
---|---|
Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
ISSN: | 0022-1899 |
DOI: | 10.1093/infdis/154.3.437 |