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Poor efficacy of intradermal administration of recombinant hepatitis B virus immunization in HIV-infected individuals who fail to respond to intramuscular administration of hepatitis B virus vaccine.

Poor efficacy of intradermal administration of recombinant hepatitis B virus immunization in HIV-infected individuals who fail to respond to intramuscular administration of hepatitis B virus vaccine. Research Abstract Details 

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  • Poor efficacy of intradermal administration of recombinant hepatitis B virus immunization in HIV-infected individuals who fail to respond to intramuscular administration of hepatitis B virus vaccine. Abstract Text:

    s d shafranS D Shafran,l d mashinterL D Mashinter,a lindemulderA Lindemulder,g d taylorG D Taylor,i chiuI Chiu,s d shafranS D Shafran,l d mashinterL D Mashinter,a lindemulderA Lindemulder,g d taylorG D Taylor,i chiuI Chiu,

    OBJECTIVE: It is recommended that hepatitis B virus (HBV)-susceptible, HIV-infected persons be immunized for HBV. However, 44-76% of HIV-infected persons fail to respond to a standard series of recombinant HBV vaccine. Intradermal (i.d.) administration of HBV vaccine has been effective in nonresponders to intramuscularly administered vaccine among healthcare workers, haemodialysis patients and renal transplant recipients. We evaluated the immunogenicity of HBV vaccine given by the intradermal route in HIV-infected individuals who failed to respond to two series of HBV vaccine given intramuscularly. METHODS: Recombinant HBV vaccine [10 microg HBV surface antigen (HBsAg)/mL] was administered as 0.25 mL i.d. every 2 weeks for four doses in 12 HIV-infected adults who failed to respond to six doses of HBV vaccine administered by the intramuscular route. Anti-HBs was tested at least 2 weeks following the fourth dose of i.d. administered vaccine, and if the anti-HBs titre was negative or <30 IU/L, a second series of four i.d. doses were administered every 2 weeks. Anti-HBs was measured at least 2 weeks following the second series of i.d. administered HBV vaccine and 6 and 12 months after the last dose. RESULTS: Protective levels of anti-HBs (>10 IU/L) were achieved in six subjects (50%) after four doses. Administration of four additional i.d. doses to the six nonresponders did not result in any additional seroconverters. Five of the six responders had no detectable anti-HBs at 12 months after the last dose of i.d. administered vaccine. CONCLUSIONS: The i.d. route of administration of recombinant HBV vaccine does not appear to be immunogenic in HIV-infected adults who fail to respond to six doses of intramuscularly administered vaccine.

    Poor efficacy of intradermal administration of recombinant hepatitis B virus immunization in HIV-infected individuals who fail to respond to intramuscular administration of hepatitis B virus vaccine. Publishing Authors By Initials

    sd shafranSD Shafran,ld mashinterLD Mashinter,a lindemulderA Lindemulder,gd taylorGD Taylor,i chiuI Chiu,sd shafranSD Shafran,ld mashinterLD Mashinter,a lindemulderA Lindemulder,gd taylorGD Taylor,i chiuI Chiu,

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    Poor efficacy of intradermal administration of recombinant hepatitis B virus immunization in HIV-infected individuals who fail to respond to intramuscular administration of hepatitis B virus vaccine. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: HIV medicine

    VOLUME: 8

    Page Numbers: 295-9

    Journal Abbreviation: HIV Med.

    ISSN: 1464-2662

    DAY: 12

    MONTH: Jul

    YEAR: 2007

    Poor efficacy of intradermal administration of recombinant hepatitis B virus immunization in HIV-infected individuals who fail to respond to intramuscular administration of hepatitis B virus vaccine. Information

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    LANGUAGE: eng

    NlmUniqueID: 100897392

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    Grant and Affiliation Information for Poor efficacy of intradermal administration of recombinant hepatitis B virus immunization in HIV-infected individuals who fail to respond to intramuscular administration of hepatitis B virus vaccine.

    AFFILIATION: Division of Infectious Diseases, Department of Medicine, University of Alberta, Edmonton, Alberta, Canada. sshafran@ualberta.ca

    Country: England

    England Research PublicationEngland Research Publication

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    MEDLINETA: HIV Med

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