CPG 7909 Adjuvant plus Hepatitis B Virus Vaccination in HIV-Infected Adults Achieves Long-Term Seroprotection for Up to 5 Years

• Published in: Clinical infectious diseases Vol. 46; no. 8; pp. 1310 - 1314
• Main Authors: Cooper, C. L., Angel, J. B., Seguin, I., Davis, H. L., Cameron, D. W.
• Format: Journal Article
• Language: English
• Published: Chicago, IL The University of Chicago Press 15.04.2008; University of Chicago Press; Oxford University Press
• Subjects: Adolescent; Adult; Adults; Antibodies; Biological and medical sciences; Dosage; Double-Blind Method; Female; Geometric mean; Hepatitis; Hepatitis B; Hepatitis B Vaccines - administration & dosage; Hepatitis B Vaccines - immunology; Hepatitis B virus; Hepatology; HIV; HIV Infections - immunology; HIV Infections - prevention & control; HIV/AIDS; Human immunodeficiency virus; Human viral diseases; Humans; Immunization; Immunodeficiencies; Immunodeficiencies. Immunoglobulinopathies; Immunopathology; Infections; Infectious diseases; Liver; Male; Medical sciences; Middle Aged; Oligodeoxyribonucleotides - administration & dosage; Oligodeoxyribonucleotides - immunology; Pharmaceutical preparations; Surface antigens; Time Factors; Treatment Outcome; Vaccination; Vaccination - methods; Viral diseases; Viral diseases of the lymphoid tissue and the blood. Aids; Viral hepatitis; Human; Immunopathology; Drug combination; Vaccination; Orthohepadnavirus; Hepatic disease; AIDS; Immune deficiency; Long term; Infection; Prevention; Virus; Viral hepatitis B; Immunoprophylaxis; Hepadnaviridae; Viral disease; Digestive diseases; Adult; Hepatitis B virus
• ISSN: 1058-4838; 1537-6591; 1537-6591
• DOI: 10.1086/533467

Background. Human immunodeficiency virus (HIV)–infected persons are hyporesponsive to hepatitis B virus (HBV) vaccination. CPG 7909 is an oligodeoxynucleotide containing immunostimulatory CpG motifs that activate human B and plasmacytoid dendritic cells via Toll-like receptor 9. We previously reported that addition of CPG 7909 to a commercial HBV vaccine enhanced the kinetics, magnitude, and longevity of the seroprotective response over 48 weeks. We now report data for the 5-year period following vaccination. Methods. A randomized, double-blind, controlled trial was conducted to determine clinical safety and immunogenicity of HBV vaccine in adult HIV-infected subjects receiving effective antiretroviral therapy. HBV-susceptible subjects, one-half of whom had experienced previous vaccination failure, were vaccinated at 0, 1, and 2 months with a double adult dose of recombinant HBV vaccine, with or without 1 mg of CPG 7909 (19 subjects per arm). Titers of antibody to HBV surface antigen (anti-HBs) were measured at 6-month intervals for up to 60 months. Results. The proportion of participants achieving and retaining seroprotection (surface antibody titers, ⩾10 mIU/mL) was greater in CPG 7909 recipients (P<.05 at all time points). Geometric mean anti-HBs titers were higher in the CPG 7909 group than in the control group (without CPG 7909 adjuvant) at all measured time points. Conclusions. The immunostimulatory properties of CPG 7909 present an important strategy in achieving long-term protection in HIV-infected patients and other HBV vaccine–hyporesponsive populations.