2010
DOI: 10.4161/hv.6.11.12849
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Persistence of immune responses after a single dose of Novartis meningococcal serogroup A, C, W-135 and Y CRM-197 conjugate vaccine (Menveo®) or Menactra® among healthy adolescents

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Cited by 76 publications
(60 citation statements)
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“…20,23,31,32 Measures of immunogenicity by rSBA after MenACWY-CRM have yielded much higher titers with prolonged persistence of antibodies. 33 However, the clinical relevance of these differences between serogroup responses are yet to be determined.…”
Section: Discussionmentioning
confidence: 99%
“…20,23,31,32 Measures of immunogenicity by rSBA after MenACWY-CRM have yielded much higher titers with prolonged persistence of antibodies. 33 However, the clinical relevance of these differences between serogroup responses are yet to be determined.…”
Section: Discussionmentioning
confidence: 99%
“…Four clinical trials conducted in adolescents 11-18 y of age [13][14][15] and children 6-10 and 2-5 y of age 12,16 show a trend of high hSBA titers immediately post-vaccination, with an age-and serogroup-specific decline in titers up to 1 year, followed by relatively stable levels up to 5 y post-vaccination. In adolescents and children 2 y of age and older, the waning of bactericidal antibody titers over time was most pronounced for serogroup A, and, to a lesser extent, serogroup C.…”
Section: Persistence Of Antibodies After a Single Dose Of Menacwy-crmmentioning
confidence: 99%
“…[7][8][9][10] This review appraises data from 7 phase 3 and phase 4 studies, with the objective of providing an overview of antibody persistence following primary vaccination with MenACWY-CRM vaccine, and responses to booster doses of the vaccine. 9,10,[11][12][13][14][15][16][17][18][19] Only data pertaining to the recommended dose schedules of MenACWY-CRM in each age group is assessed here : a single dose in children 2-10 y of age, adolescents and adults; 4 doses at 2, 4, 6 and 12 months of age in infants; and 2 doses given to unvaccinated children between 7-23 months of age. All the studies included in this review were conducted in accordance with good clinical practice and International Conference on Harmonisation of Techniques for Requirements for Registration of Pharmaceuticals for Human Use guidelines, and were approved by Institutional Review Boards (IRBs) or Ethics Committees (ECs) in each country, as appropriate, prior to start of the study.…”
Section: Introductionmentioning
confidence: 99%
“…Reactions, n (%) 68 (40) 12 (32) 30 (45) 26 (39) chills, any 16 (9) 3 (8) 5 (8) 8 (12) chills, severe 1 (27) 18 (27) headache, severe 2 (1) 1 ( …”
Section: Methodsmentioning
confidence: 99%