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A Third Dose of Measles-Mumps-Rubella Vaccine to Improve Immunity Against Mumps in Young Adults.
Kaaijk, Patricia; Wijmenga-Monsuur, Alienke J; van Houten, Marlies A; Veldhuijzen, Irene K; Ten Hulscher, Hinke I; Kerkhof, Jeroen; van der Klis, Fiona R; van Binnendijk, Rob S.
Afiliação
  • Kaaijk P; Center for Infectious Disease Control, National Institute for Public Health and the Environment, Bilthoven.
  • Wijmenga-Monsuur AJ; Center for Infectious Disease Control, National Institute for Public Health and the Environment, Bilthoven.
  • van Houten MA; Department of Pediatrics, Spaarne Hospital, Hoofddorp, the Netherlands.
  • Veldhuijzen IK; Center for Infectious Disease Control, National Institute for Public Health and the Environment, Bilthoven.
  • Ten Hulscher HI; Center for Infectious Disease Control, National Institute for Public Health and the Environment, Bilthoven.
  • Kerkhof J; Center for Infectious Disease Control, National Institute for Public Health and the Environment, Bilthoven.
  • van der Klis FR; Center for Infectious Disease Control, National Institute for Public Health and the Environment, Bilthoven.
  • van Binnendijk RS; Center for Infectious Disease Control, National Institute for Public Health and the Environment, Bilthoven.
J Infect Dis ; 221(6): 902-909, 2020 03 02.
Article em En | MEDLINE | ID: mdl-31112277
ABSTRACT

BACKGROUND:

Waning of vaccine-induced immunity is considered to play a central role in the reemergence of mumps among vaccinated young adults. The aim of the present study was to investigate antibody responses and safety of a third dose of measles-mumps-rubella vaccine (MMR-3) in 150 young adults. Antibody levels were related to a surrogate of protection based on preoutbreak serum antibody levels in 31 persons with and 715 without serological evidence of mumps.

METHODS:

Mumps virus-specific immunoglobulin G (IgG) antibody responses and mumps virus-neutralizing antibody responses (based on the focus-reduction neutralizing test) against both the Jeryl Lynn mumps virus vaccine strain (hereafter, the "vaccine strain") and the MuVi/Utrecht.NLD/40.10 outbreak strain (hereafter, the "outbreak strain") were determined, and vaccine safety was evaluated.

RESULTS:

Four weeks following MMR-3 receipt, levels of IgG, anti-vaccine strain, and anti-outbreak strain antibodies increased by a factor of 1.65, 1.34, and 1.35, respectively. Although antibody levels decreased 1 year later, they were still above the baseline level by a factor of 1.37, 1.15, and 1.27, respectively. Based on the surrogate protective antibody cutoff, significantly more participants were protected against mumps virus infection up to 1 year after vaccination (ie, they had antibody levels above the presumed threshold for herd immunity).

CONCLUSIONS:

MMR-3 receipt increased antibody levels that may protect against mumps virus infection for longer than previously assumed and is expected to be a good and safe intervention for controlling a mumps outbreak. CLINICAL TRIALS REGISTRATION 2016-001104-36; NTR5911.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vacina contra Sarampo-Caxumba-Rubéola / Caxumba Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vacina contra Sarampo-Caxumba-Rubéola / Caxumba Idioma: En Ano de publicação: 2020 Tipo de documento: Article