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Vaccines

Serum Bactericidal Antibody Responses of Adults Immunized with the MenB-4C Vaccine against Genetically Diverse Serogroup B Meningococci

Serena Giuntini, Eduardo Lujan, Malick M. Gibani, Christina Dold, Christine S. Rollier, Andrew J. Pollard, Dan M. Granoff
Kathryn M. Edwards, Editor
Serena Giuntini
aCenter for Immunobiology and Vaccine Development, UCSF Benioff Children's Hospital Oakland, Oakland, California, USA
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Eduardo Lujan
aCenter for Immunobiology and Vaccine Development, UCSF Benioff Children's Hospital Oakland, Oakland, California, USA
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Malick M. Gibani
bOxford Vaccine Group, Department of Paediatrics, University of Oxford, and the NIHR Oxford Biomedical Research Centre, Oxford, United Kingdom
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Christina Dold
bOxford Vaccine Group, Department of Paediatrics, University of Oxford, and the NIHR Oxford Biomedical Research Centre, Oxford, United Kingdom
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Christine S. Rollier
bOxford Vaccine Group, Department of Paediatrics, University of Oxford, and the NIHR Oxford Biomedical Research Centre, Oxford, United Kingdom
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Andrew J. Pollard
bOxford Vaccine Group, Department of Paediatrics, University of Oxford, and the NIHR Oxford Biomedical Research Centre, Oxford, United Kingdom
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Dan M. Granoff
aCenter for Immunobiology and Vaccine Development, UCSF Benioff Children's Hospital Oakland, Oakland, California, USA
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Kathryn M. Edwards
Vanderbilt University Medical Center
Roles: Editor
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DOI: 10.1128/CVI.00430-16
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ABSTRACT

MenB-4C is a meningococcal vaccine for the prevention of serogroup B disease. The vaccine contains factor H binding protein (FHbp) and three other antigens that can elicit serum bactericidal antibodies (SBA). For vaccine licensure, efficacy was inferred from the SBA responses against three antigen-specific indicator strains. The relation between those results and broad protection against circulating genetically diverse strains is not known. Twenty adults were immunized with two doses of MenB-4C given 1 to 2 months apart. SBA activity against 3 reference strains and 15 serogroup B test strains (6 from college outbreaks) was measured. Compared to the preimmunization titers, 70%, 95%, and 95% of subjects had ≥4-fold increases in the titers of anti-PorA P1.4, anti-NadA, and anti-FHbp antibodies against the reference strains, respectively. In contrast, only 25 to 45% of the subjects had ≥4-fold increases in responses to 10 of the 15 test strains, including 8 that expressed one to three of the antigens in the vaccine. At 1 month, the majority of subjects with <4-fold titer increases had serum titers of ≥1:4, which are considered sufficient for protection. However, the titers against four strains declined to <1:4 by 4 to 6 months in one-third to greater than 50% of the subjects tested. Clinically relevant isolates are often more resistant to SBA than the indicator strains used to measure antigen-specific SBA. A working model is that the percentage of subjects with titers of ≥1:4 at 1 month postimmunization correlates with short-term protection against that strain, whereas the percentage of subjects with ≥4-fold titer increases represents a more robust response. (The protocol used at the Oxford Vaccine Group has been registered at ClinicalTrials.gov under registration no. NCT02398396.)

FOOTNOTES

    • Received 1 September 2016.
    • Returned for modification 21 September 2016.
    • Accepted 4 November 2016.
    • Accepted manuscript posted online 9 November 2016.
  • Supplemental material for this article may be found at https://doi.org/10.1128/CVI.00430-16 .

  • Copyright © 2017 American Society for Microbiology.

All Rights Reserved .

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Serum Bactericidal Antibody Responses of Adults Immunized with the MenB-4C Vaccine against Genetically Diverse Serogroup B Meningococci
Serena Giuntini, Eduardo Lujan, Malick M. Gibani, Christina Dold, Christine S. Rollier, Andrew J. Pollard, Dan M. Granoff
Clinical and Vaccine Immunology Jan 2017, 24 (1) e00430-16; DOI: 10.1128/CVI.00430-16

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Serum Bactericidal Antibody Responses of Adults Immunized with the MenB-4C Vaccine against Genetically Diverse Serogroup B Meningococci
Serena Giuntini, Eduardo Lujan, Malick M. Gibani, Christina Dold, Christine S. Rollier, Andrew J. Pollard, Dan M. Granoff
Clinical and Vaccine Immunology Jan 2017, 24 (1) e00430-16; DOI: 10.1128/CVI.00430-16
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    • ABSTRACT
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KEYWORDS

Antibody Formation
Blood Bactericidal Activity
Genotype
Meningococcal Vaccines
Neisseria meningitidis, Serogroup B
MenB-4C
Bexsero
complement factor H
FH
FHbp
factor H binding protein
autoantibody
meningococcal vaccine

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