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1.
NIPH Ann ; 14(2): 67-79; discussion 79-80, 1991 Dec.
Article in English | MEDLINE | ID: mdl-1812438

ABSTRACT

A vaccine against serogroup B meningococcal disease has been prepared from a B:15:P1.7,16 meningococcal strain (44/76) by fermentor growth and extraction of the bacteria with the detergent deoxycholate. Outer membrane vesicles (OMV) were purified by ultracentrifugation and adsorbed to aluminium hydroxide adjuvant. OMV contained the major class 1, 3, 4 and 5 proteins and some minor high molecular weight protein components. Relative to protein, the vaccine also contained about 8% phospholipid, 7% lipopolysaccharide and 16% deoxycholate. The product was generally non-pyrogenic to humans in ordinary doses and was highly immunogenic in mice and humans. Production and control steps, physical, chemical and immunological data for the vaccine are described.


Subject(s)
Bacterial Outer Membrane Proteins/immunology , Bacterial Vaccines/standards , Meningitis, Meningococcal/prevention & control , Polysaccharides, Bacterial/immunology , Bacterial Capsules , Bacterial Outer Membrane Proteins/chemistry , Bacterial Outer Membrane Proteins/isolation & purification , Bacterial Vaccines/biosynthesis , Bacterial Vaccines/chemistry , Drug Evaluation , Humans , Immunoblotting , Incidence , Meningitis, Meningococcal/epidemiology , Meningitis, Meningococcal/microbiology , Meningococcal Vaccines , Norway/epidemiology , Quality Control , Serotyping
2.
Lancet ; 338(8775): 1093-6, 1991 Nov 02.
Article in English | MEDLINE | ID: mdl-1682541

ABSTRACT

For more than 15 years, Norway has had the highest incidence of meningococcal disease in northern Europe, with 80% of cases being due to serogroup B meningococci. The case-fatality has remained high, at about 10%. In this study, an outer membrane vaccine, which had previously been shown to induce an increase in bactericidal antibodies to the parent strain, was assessed in a large-scale, randomised, double-blind trial. From October, 1988, 171,800 students in secondary schools volunteered to take part in a double-blind, placebo-controlled, efficacy trial with school as the randomisation unit. Hospitals and clinics that routinely receive patients with infectious disease were asked to report urgently all cases of suspected meningitis and/or septicaemia in 13-21-year-old students in Norway. These cases were registered and further investigated according to a detailed protocol. 89 out of the 221 cases investigated by June 3, 1991, were shown to be severe systemic disease due to group B meningococci. 36 cases in 35 schools took part in the trial (11 schools with vaccinated students and 24 with students given placebo). The calculated rate of protection was thus 57.2% (p = 0.012, one-sided test). The findings suggest that, although the vaccine conferred protection against group B meningococcal disease, the effect was insufficient to justify a public vaccination programme.


Subject(s)
Antigens, Bacterial/administration & dosage , Bacterial Outer Membrane Proteins/administration & dosage , Bacterial Vaccines/administration & dosage , Disease Outbreaks/prevention & control , Meningitis, Meningococcal/prevention & control , Neisseria meningitidis/immunology , Polysaccharides, Bacterial/administration & dosage , Vaccination , Adolescent , Adult , Bacterial Capsules , Child , Child, Preschool , Double-Blind Method , Evaluation Studies as Topic , Follow-Up Studies , Humans , Immunization Schedule , Infant , Meningitis, Meningococcal/epidemiology , Meningococcal Vaccines , Norway/epidemiology
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