Recurrent Genital Herpes and Suppressive Oral Acyclovir Therapy

Relation Between Clinical Outcome and In-Vitro Drug Sensitivity

  1. SANDRA NUSINOFF LEHRMAN, M. D.;
  2. JOHN M. DOUGLAS, M.D.;
  3. LAWRENCE COREY, M.D.; and
  4. DAVID W. BARRY, M.D.
  1. Research Triangle Park, North Carolina; Denver, Colorado; and Seattle, Washington

    Abstract

    To evaluate the association between in-vitro resistance of herpes simplex virus type 2 to acyclovir and breakthrough recurrences of herpes despite chronic suppressive therapy, we determined the in-vitro sensitivity of herpes simplex virus isolated before, during, and after therapy. One hundred eighty-three virus isolates from 107 patients were tested. Before therapy, the median amount of drug required to inhibit 50% of the virus in tissue culture (ID50) was 0.91 µg/mL. The median ID50 after therapy was 0.99. Six isolates from patients with culture-positive breakthrough recurrences were evaluated. The median ID50 was 0.90 µg/mL (range, 0.39 to 1.55). The development of breakthrough recurrences could not be correlated with infection with strains of herpes simplex virus type 2 that were resistant to acyclovir in vitro. Acyclovir-resistant strains are not commonly recovered from patients during acyclovir therapy, nor does there seem to be a high frequency of resistance after 4 months of chronic suppressive therapy.

    Article and Author Information

    • ▸From the Department of Virology, The Wellcome Research Laboratories, Research Triangle Park, North Carolina; Disease Control Service, Denver Department of Health and Hospitals, Denver, Colorado; and the Departments of Laboratory Medicine, Microbiology, and Medicine, University of Washington and Children's Orthopedic Hospital, Seattle, Washington.

    • ▸Requests for reprints should be addressed to Sandra Nusinoff Lehrman, M.D.; Department of Virology, Burroughs Wellcome Company, 3030 Cornwallis Road; Research Triangle Park, NC 27709.

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