The effect of treatment with zidovudine with or without acyclovir on HIV p24 antigenaemia in patients with AIDS or AIDS-related complex. NLM AIDSLINE Important note: Information in this article was accurate in 1993. The state of the art may have changed since the publication date.

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The effect of treatment with zidovudine with or without acyclovir on HIV p24 antigenaemia in patients with AIDS or AIDS-related complex.

AIDS. 1992 Aug;6(8):821-5. Unique Identifier : AIDSLINE MED/93039866
Pedersen C; Cooper DA; Brun-Vezinet F; Doherty R; Skinhoj P; Perol Y; Luthy R; Leibowitch J; Habermehl KO; Varnier OE; et al; Hvidovre Hospital, Copenhagen, Denmark.


Abstract: OBJECTIVE: To evaluate changes in serum HIV p24-antigen levels in a subset of patients who participated in a European/Australian double-blind, placebo-controlled trial evaluating the efficacy of zidovudine (250 mg every 6 h) alone or in combination with acyclovir (800 mg every 6 h) in patients with AIDS, AIDS-related complex (ARC) or Kaposi's sarcoma (KS). DESIGN: Double-blind, placebo-controlled randomized clinical trial of less than or equal to 6 months' therapy. SETTING: Samples were obtained from patients attending teaching hospital outpatient clinics in seven European countries and Australia. SUBJECTS: One hundred and ninety-seven HIV-infected patients (60 with AIDS and 137 with ARC or KS). MAIN OUTCOME MEASURES: Serum HIV p24-antigen levels measured using the Abbott HIV solid-phase enzyme immunoassay. RESULTS: Of 76 ARC/KS patients who were initially HIV p24-antigen-positive, one out of 25 randomized to placebo, eight out of 23 to zidovudine and 11 out of 28 to the zidovudine/acyclovir combination became antigen-negative. The proportion of patients who became antigen-negative was significantly higher in both the zidovudine group (P = 0.016) and the zidovudine/acyclovir group (P = 0.004), compared with the placebo group. There were no statistical differences between the zidovudine and the zidovudine/acyclovir groups. During the trial p24-antigen levels in the zidovudine-treated patients reached their minimum after 4-8 weeks of therapy, and tended to increase gradually thereafter. Disease progression occurred irrespective of whether p24-antigen levels declined during therapy. No association between p24-antigen responses to therapy and baseline disease stage, Karnofsky score or baseline CD4 cell count was detectable. CONCLUSION: Acyclovir does not potentiate the effect of zidovudine on p24-antigen levels. Change in antigen level in response to antiviral therapy needs further investigation before it is used as a surrogate marker for clinical efficacy of antiviral therapy.
Keywords: Acquired Immunodeficiency Syndrome/*DRUG THERAPY/IMMUNOLOGY Acyclovir/PHARMACOLOGY/*THERAPEUTIC USE AIDS-Related Complex/*DRUG THERAPY/IMMUNOLOGY Double-Blind Method Drug Therapy, Combination Human HIV Core Protein p24/*BLOOD/DRUG EFFECTS Zidovudine/PHARMACOLOGY/*THERAPEUTIC USE CLINICAL TRIAL JOURNAL ARTICLE MULTICENTER STUDY RANDOMIZED CONTROLLED TRIALKWDacquiredimmunodeficiencysyndrome/KWDdrugtherapy/immunologyacyclovir/pharmacology/KWDtherapeuticuseaids-relatedcomplex/KWDdrugtherapy/immunologydouble-blindmethoddrugtherapy,combinationhumanhivcoreproteinp24/KWDblood/drugeffectszidovudine/pharmacology/KWDtherapeuticuseclinicaltrialjournalarticlemulticenterstudyrandomizedcontrolledtrial
930228
M9320828

Copyright © 1993 - National Library of Medicine. Reproduced under license with the National Library of Medicine, Bethesda, MD.

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