Literature DB >> 25553243

Prevention of rare diseases: how revolutionary techniques can help vulnerable individuals-the example of serogroup B meningococcal infection.

E David McIntosh1, Victor Carey2, Daniela Toneatto2, Peter Dull2, James Wassil2.   

Abstract

In countries with established programmes for vaccination of infants, toddlers and adolescents with meningococcal conjugate vaccines, serogroup B invasive meningococcal disease remains the major cause of septicaemia and meningitis in the paediatric and adolescent age groups. Novartis has developed a serogroup B meningococcal vaccine, 4CMenB, to meet this need. We reviewed all 4CMenB studies. The studies found 4CMenB to be highly immunogenic when administered in all schedules, with protective antibody levels (serum bactericidal antibody titres ≥4 or ≥5 with human complement, hSBA) against serogroup B strains expressing vaccine antigens in >95% of vaccinated cohorts. When antibody levels waned, all tested groups demonstrated booster responses. Although possibly an underestimation, the Meningococcal Antigen Typing System (MATS) technique predicts that global coverage of 4CMenB against all serogroup B strains is in the range 66% (Canada) to 91% (USA). The vaccine was found to be generally well tolerated, although local and systemic reactions, notably fever in infants, typical of many vaccines, were increased following concomitant administration of 4CMenB with routine vaccines. When tested, prophylactic paracetamol significantly decreased the frequency and severity of reactions in infants, with no clinically significant impact on immunogenicity of 4CMenB or concomitant routine vaccines. The vaccine is approved for use in the following age groups in the European Union (2 months+), Canada (2 months through 17 years), Australia (2 months+) and Chile (2 months+), following clinical evaluation in 4843 infants and toddlers, and 1712 adolescents and adults, in schedules including a three-dose (2, 3, 4 or 2, 4, 6 months) and a two-dose (6-11 months) infant series with a booster in the second year of life, a two-dose series in toddlers (12-23 months) and children (2-10 years) given 2 months apart (with a booster at least in the EU), and a two-dose series in adolescents (11-17 years) given 1-6 months apart. 4CMenB presents a solution to the unmet medical need of offering protection against serogroup B invasive meningococcal disease in all age groups above 2 months.

Entities:  

Keywords:  immunization; meningitis; meningococcal infection; meningococcus; rare disease; reverse vaccinology; vaccination; vulnerable individual

Year:  2015        PMID: 25553243      PMCID: PMC4266687          DOI: 10.1177/2051013614557477

Source DB:  PubMed          Journal:  Ther Adv Vaccines        ISSN: 2051-0136


  55 in total

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Authors:  Carmen Baccarini; Andrew Ternouth; Heather Wieffer; Andrew Vyse
Journal:  Hum Vaccin Immunother       Date:  2012-10-29       Impact factor: 3.452

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Journal:  Vaccine       Date:  2013-04-06       Impact factor: 3.641

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  2 in total

1.  Need for Optimisation of Immunisation Strategies Targeting Invasive Meningococcal Disease in the Netherlands.

Authors:  Josefien Cornelie Minthe Bousema; Joost Ruitenberg
Journal:  Int J Health Policy Manag       Date:  2015-09-13

Review 2.  Recommended vaccinations for asplenic and hyposplenic adult patients.

Authors:  Paolo Bonanni; Maddalena Grazzini; Giuditta Niccolai; Diana Paolini; Ornella Varone; Alessandro Bartoloni; Filippo Bartalesi; Maria Grazia Santini; Simonetta Baretti; Carlo Bonito; Paola Zini; Maria Teresa Mechi; Fabrizio Niccolini; Lea Magistri; Maria Beatrice Pulci; Sara Boccalini; Angela Bechini
Journal:  Hum Vaccin Immunother       Date:  2017-02       Impact factor: 3.452

  2 in total

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