4.5 Article

Safety and efficacy of a cytomegalovirus glycoprotein B (gB) vaccine in adolescent girls: A randomized clinical trial

期刊

VACCINE
卷 34, 期 3, 页码 313-319

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.vaccine.2015.11.056

关键词

Cytomegalovirus; Vaccine; Adolescent; CMV gB

资金

  1. NIAID/NIH/HHS [HHSN272200800006C, HHSN272200800002C, HHSN27220080000C, HHSN272200800013C]
  2. Biomedical Advanced Research and Development Authority, Department of Health and Human Services
  3. CTSA grant from NIH [UL1 RR024975-01]
  4. KL2 CCTS Supplement Award [3KL2RR024149-05S1]

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Background: Cytomegalovirus (CMV) is a leading cause of congenital infection and an important target for vaccine development. Methods: CMV seronegative girls between 12 and 17 years of age received CMV glycoprotein B (gB) vaccine with MF59 or saline placebo at 0, 1 and 6 months. Blood and urine were collected throughout the study for evidence of CMV infection based on PCR and/or seroconversion to non-vaccine CMV antigens. Results: 402 CMV seronegative subjects were vaccinated (195 vaccine, 207 placebo). The vaccine was generally well tolerated, although local and systemic adverse events were significantly more common in the vaccine group. The vaccine induced gB antibody in all vaccine recipients with a gB geometric mean titer of 13,400 EU; 95%CI 11,436, 15,700, after 3 doses. Overall, 48 CMV infections were detected (21 vaccine, 27 placebo). In the per protocol population (124 vaccine, 125 placebo) vaccine efficacy was 43%; 95%CI: -36; 76, p = 0.20. The most significant difference was after 2 doses, administered as per protocol; vaccine efficacy 45%, 95%CI: -9; 72, p = 0.08. Conclusion: The vaccine was safe and immunogenic. Although the efficacy did not reach conventional levels of significance, the results are consistent with a previous study in adult women (Pass et al. N Engl J Med 2009;360:1191) using the same formulation. (C) 2015 Elsevier Ltd. All rights reserved.

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