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METHODS:
Young adults aged 18-31 years with documented two doses of MMR vaccine received a third
dose of MMR vaccine between July 2009 and October 2010. Rubella neutralizing antibody titers
were assessed before, 1 month, and 1 year after receipt of a third dose of MMR vaccine.
RESULTS:
Among 679 participants, 1.8% had rubella antibody titers less than 10 U/ml, immediately before
vaccination, approximately 15 years after receipt of a second dose of MMR vaccine. One month
after receipt of a third dose of MMR vaccine, average titers were 4.5 times higher and >50% of
participants had a 4-fold boost. Response was highest among those with titers less than 10 U/ml
prior to vaccination (geometric mean titer ratio = 18.8; 92% seroconversion) and decreased with
increasing pre-vaccination titers. Average titers declined 1 year postvaccination but remained
significantly higher than pre-vaccination levels. The proportion classified as low-positive antibody
levels increased from 3% 1 month postvaccination to 24% 1 year postvaccination.
CONCLUSIONS:
Vaccination with a third dose of MMR vaccine resulted in a robust boosting of rubella neutralizing
antibody response that remained elevated 1 year later. Young adults with low rubella titers are
more likely to benefit from a third dose of MMR vaccine.
Copyright © 2018 Elsevier Ltd. All rights reserved.
KEYWORDS:
Immune response; Rubella; Third-dose measles-mumps-rubella (MMR) vaccine
PMID:
30107992
DOI:
10.1016/j.vaccine.2018.08.010
[Indexed for MEDLINE]
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Publication type
MeSH terms
Adolescent
Adult
Antibodies, Neutralizing/blood*
Antibodies, Viral/blood*
Female
Humans
Immunization Schedule*
Immunization, Secondary/methods*
Male
Measles-Mumps-Rubella Vaccine/administration & dosage*
Rubella/immunology
Rubella/prevention & control
Rubella virus/immunology*
Vaccination
Young Adult
Substances
Antibodies, Neutralizing
Antibodies, Viral
Measles-Mumps-Rubella Vaccine
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Medical
PMID:
29491021
PMCID:
PMC5925731
DOI:
10.1128/JCM.01954-17
[Indexed for MEDLINE]
Free PMC Article
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MeSH terms
Adolescent
Adult
Aged
Antibodies, Viral/blood
British Columbia/epidemiology
Child
Child, Preschool
Disease Outbreaks*
Female
Genes, Viral/genetics
Genetic Variation
Genotype
Humans
Immunoglobulin M/blood
Infant
Male
Measles-Mumps-Rubella Vaccine/genetics
Measles-Mumps-Rubella Vaccine/isolation & purification
Middle Aged
Mumps/diagnosis*
Mumps/epidemiology*
Mumps/virology
Mumps virus/classification
Mumps virus/genetics*
Mumps virus/immunology
RNA, Viral/genetics
Reverse Transcriptase Polymerase Chain Reaction
Vaccination/statistics & numerical data
Young Adult
Substances
Antibodies, Viral
Immunoglobulin M
Measles-Mumps-Rubella Vaccine
RNA, Viral
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HighWire
Europe PubMed Central
PubMed Central
Medical
PMID:
29206078
PMCID:
PMC5893213
DOI:
10.1080/21645515.2017.1412021
[Indexed for MEDLINE]
Free PMC Article
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Publication type
MeSH terms
Adolescent
Adult
Aged
Antibodies, Viral/blood*
Antibodies, Viral/immunology*
Czech Republic
Disease Outbreaks/prevention & control
Female
Humans
Immunization Programs/methods
Male
Measles/immunology
Measles/prevention & control
Measles-Mumps-Rubella Vaccine/immunology
Middle Aged
Mumps/blood
Mumps/immunology*
Mumps/prevention & control*
Mumps virus/immunology
Seroepidemiologic Studies
Surveys and Questionnaires
Vaccination/methods
Young Adult
Substances
Antibodies, Viral
Measles-Mumps-Rubella Vaccine
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Medical
PMID:
29868358
PMCID:
PMC5984205
DOI:
10.1016/j.pmedr.2018.02.005
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Elsevier Science
ClinicalKey
Europe PubMed Central
PubMed Central
J Infect Dis. 2016 Apr 1;213(7):1115-23. doi: 10.1093/infdis/jiv555. Epub 2015 Nov 23.
METHODS:
Measles virus (MeV) neutralizing antibody concentrations, cell-mediated immunity (CMI), and
immunoglobulin G (IgG) antibody avidity were assessed at baseline and 1 month and 1 year after
MMR3 receipt.
RESULTS:
Of 662 subjects at baseline, 1 (0.2%) was seronegative for MeV-neutralizing antibodies (level, <8
mIU/mL), and 23 (3.5%) had low antibody levels (8-120 mIU/mL). One month after MMR3
receipt, 1 subject (0.2%) was seronegative, and 6 (0.9%) had low neutralizing antibodies, with
only 21 of 662 (3.2%) showing a ≥ 4-fold rise in neutralizing antibodies. One year after MMR3
receipt, no subject was seronegative, and 10 of 617 (1.6%) had low neutralizing antibody levels.
CMI analyses showed low levels of spot-forming cells after stimulation, suggesting the presence
of T-cell memory, but the response was minimal after MMR3 receipt. MeV IgG avidity did not
correlate with findings of neutralization analyses.
CONCLUSIONS:
Most subjects were seropositive before MMR3 receipt, and very few had a secondary immune
response after MMR3 receipt. Similarly, CMI and avidity analyses showed minimal qualitative
improvements in immune response after MMR3 receipt. We did not find compelling data to
support a routine third dose of MMR vaccine.
Published by Oxford University Press for the Infectious Diseases Society of America 2015. This work is
written by (a) US Government employee(s) and is in the public domain in the US.
KEYWORDS:
cell-mediated immunity; immunization; measles; measles vaccine immunogenicity;
measles virus antibody avidity; third dose of measles,
mumps, rubella (MMR) vaccine; vaccine-preventable disease
PMID:
26597262
PMCID:
PMC5729920
DOI:
10.1093/infdis/jiv555
[Indexed for MEDLINE]
Free PMC Article
Publication type
MeSH terms
Adolescent
Adult
Antibodies, Neutralizing/blood*
Antibodies, Viral/blood*
Antibody Affinity
Cohort Studies
Female
Humans
Immunity, Cellular/physiology*
Immunization Schedule
Immunoglobulin G/blood*
Longitudinal Studies
Male
Measles virus/immunology*
Measles-Mumps-Rubella Vaccine/administration & dosage
Measles-Mumps-Rubella Vaccine/immunology*
Neutralization Tests
Odds Ratio
Young Adult
Substances
Antibodies, Neutralizing
Antibodies, Viral
Immunoglobulin G
Measles-Mumps-Rubella Vaccine
Grant support
Medical
Author information
1
Department of Urology and Comprehensive Cancer Center, Vienna General Hospital, Medical
University of Vienna, Währinger Gürtel 18-20, 1090 Vienna, Austria. andrea-
ioana.beleni@meduniwien.ac.at.
Abstract
Vaccination against mumps virus (MuV) (mostly measles-mumps-rubella) is routinely performed
in more than 120 countries and has resulted in a distinct decrease of mumps incidence.
However, alteration of mumps epidemiology has been observed in several countries after
implementation of the vaccine but is sparsely documented. Moreover, outbreaks have occurred
after starting vaccination, even in highly vaccinated populations. In the former German
Democratic Republic (DDR) mumps was a notifiable disease but vaccination against mumps was
not implemented. In the five eastern German states forming the DDR until 1990, mumps was not
notifiable until 2001. Except for the lack of reporting between 1990⁻2000, data from Eastern
Germany allow analysis of mumps epidemiology after initiating the vaccination campaign. For the
period from 2001 to 2016 the data show that the incidence of mumps dropped notably after
initiating vaccines, and was accompanied by an increase of the median age of patients with
mumps. In Eastern Germany, no outbreaks were noted, while several outbreaks occurred in
Western Germany, possibly due to a lower vaccination rate. Further literature analysis revealed
that outbreaks were facilitated by waning immunity and crowding. Nevertheless, although
vaccination prevented infection, the course of illness, once infected, was sometimes more
complicated. In comparison to non-vaccinated populations, high rates of complicated courses
occurred and were marked by orchitis, due to higher age of mumps patients. Therefore, refusing
vaccination against mumps increases the risk of severe courses when living in a vaccinated
population.
KEYWORDS:
Jeryl Lynn; Leningrad-Zagreb; Urabe; measles-mumps-rubella vaccination; orchitis;
vaccination effectiveness; waning immunity
PMID:
30065192
PMCID:
PMC6121553
DOI:
10.3390/ijerph15081618
Publication type
Review
MeSH terms
Adolescent
Adult
Aged
Aged, 80 and over
Child
Child, Preschool
Disease Outbreaks/prevention & control
Female
Germany/epidemiology
Humans
Immunization Programs/organization & administration*
Incidence
Infant
Male
Measles/epidemiology*
Measles/prevention & control*
Measles-Mumps-Rubella Vaccine/therapeutic use*
Middle Aged
Mumps/epidemiology*
Mumps/prevention & control*
Vaccination/statistics & numerical data*
Young Adult
Substance
Measles-Mumps-Rubella Vaccine
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Medical
PMID:
26047038
PMCID:
PMC4514281
DOI:
10.1080/21645515.2015.1040967
[Indexed for MEDLINE]
Free PMC Article
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Publication types
Observational Study
Research Support, Non-U.S. Gov't
MeSH terms
Adolescent
Adult
Antibodies, Neutralizing/analysis
Antibodies, Viral/analysis
Epidemics*
Female
Humans
Immunoglobulin G/analysis
Male
Middle Aged
Mumps/epidemiology*
Mumps/immunology*
Mumps/prevention & control
Mumps Vaccine/immunology*
Neutralization Tests
Vaccination
Vaccines, Combined
Young Adult
Substances
Antibodies, Neutralizing
Antibodies, Viral
Immunoglobulin G
Mumps Vaccine
Vaccines, Combined
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Medical
OBJECTIVE:
To describe the outbreak and estimate vaccine effectiveness.
METHODS:
CASE DEFINITION:
unilateral or bilateral swelling of the parotid or other salivary glands for three or more days
without any other apparent cause.
REFERENCE POPULATION:
People attending the 'Parque Goya' High School or with transmission chain origin in the High
School.
OUTBREAK PERIOD:
From two days before the onset of symptoms of the first case to five days after the last case.
Samples were collected for virus confirmation (IgM, urine culture and oropharyngeal exudate),
and isolates were processed for genotyping. A retrospective cohort study was performed in two
high school classrooms to estimate vaccine efficacy. Public health authorities conducted active
surveillance, isolation of cases, and vaccination of susceptible contacts.
RESULTS:
There were 27 cases. Twenty-one (77.8%) were vaccinated with two doses of Measles-Mumps-
Rubella vaccine. Twelve (44%) were confirmed microbiologically. G1 genotype was determined
in six cases. According to the cohort study, vaccine efficacy for one dose was 34% (95%CI: -44
to 70), and was 67% (95%CI: 28 to 83) for two doses.
CONCLUSIONS:
Vaccine effectiveness was lower than expected. Early detection and isolation of cases have been
instrumental in preventing new cases in schools.
PMID:
25475656
DOI:
10.1016/j.eimc.2014.09.011
[Indexed for MEDLINE]
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MeSH terms
Adolescent
Adult
Antibodies, Viral/blood
Child
Contact Tracing
Disease Outbreaks*
Female
Genotype
Humans
Immunoglobulin M/blood
Male
Mumps/epidemiology*
Mumps/immunology
Mumps/prevention & control
Mumps Vaccine/immunology*
Mumps virus/genetics
Mumps virus/immunology
Mumps virus/isolation & purification
Population Surveillance
Retrospective Studies
Schools
Spain/epidemiology
Vaccination/statistics & numerical data
Vaccine Potency*
Young Adult
Substances
Antibodies, Viral
Immunoglobulin M
Mumps Vaccine
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Elsevier Science
Medical
Author information
1
Shiraz Transplant Research Center, Shiraz University of Medical Sciences, Shiraz, Islamic
Republic of Iran; Gastroenterohepatology Research Center, Shiraz University of Medical
Sciences, Shiraz, Islamic Republic of Iran. dehghanism@sums.ac.ir.
Abstract
BACKGROUND/AIMS:
Generally, prevention of infections by vaccination is the least invasive and most cost-effective
approach to reduce the incidence of infections and the morbidity and mortality in transplant
recipients. Genetic diversity and different liver disease among patients contributes to variability in
immune responses to vaccines and pathogens. The aim of this study was to evaluate immunity
status to different vaccinated organisms in pediatric liver-transplant candidates.
RESULTS:
Eighty percent of the patients had protective antibody titers for poliomyelitis, 65.6% for rubella,
62.3% for diphtheria, 60% for tetanus, 57.7% for pertussis, 55.5% for measles, 42.2% for
hepatitis B and 36.7% for mumps.
CONCLUSION:
Overall seroconversion rates were not satisfactory for many infections that may be due to lower
rate of vaccination or even the underlying liver disease that interfere with optimal
immunogenecity of vaccination. Therefore, vaccination charts should be periodically reviewed
and updated, also repeated measurements of serum antibodies and appropriate revaccination if
titers decline is recommended to prevent the vaccine-preventable disease in liver transplant
candidates after transplant.
PMID:
25910330
DOI:
10.5152/tjg.2014.5139
MeSH terms
Adolescent
Antibodies, Bacterial/blood*
Antibodies, Viral/blood*
Bordetella pertussis/immunology
Child
Child, Preschool
Chronic Disease
Clostridium tetani/immunology
Corynebacterium diphtheriae/immunology
Diphtheria-Tetanus-Pertussis Vaccine/administration & dosage
Diphtheria-Tetanus-Pertussis Vaccine/immunology*
Female
Hepatitis B Vaccines/administration & dosage
Hepatitis B Vaccines/immunology*
Hepatitis B virus/immunology
Humans
Immunization Schedule
Immunocompetence
Infant
Liver Diseases/immunology*
Liver Transplantation
Male
Measles virus/immunology
Measles-Mumps-Rubella Vaccine/administration & dosage
Measles-Mumps-Rubella Vaccine/immunology*
Mumps virus/immunology
Poliovirus/immunology
Poliovirus Vaccine, Oral/administration & dosage
Poliovirus Vaccine, Oral/immunology*
Preoperative Care
Rubella virus/immunology
Vaccination
Substances
Antibodies, Bacterial
Antibodies, Viral
Diphtheria-Tetanus-Pertussis Vaccine
Hepatitis B Vaccines
Measles-Mumps-Rubella Vaccine
Poliovirus Vaccine, Oral
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Aves Yayincilik
Medical