Literature DB >> 7068216

Cross-immunogenicity of pneumococcal group 9 capsular polysaccharides in adult volunteers.

S C Szu, C J Lee, J C Parke, G Schiffman, J Henrichsen, R Austrian, S C Rastogi, J B Robbins.   

Abstract

Group 9 organisms (types 9N, 9A, 9L, and 9V) account for about 3 to 4% of pneumococcal disease isolates throughout the world. Types 9N and 9V comprise about 90% of the group 9 disease isolates. Type 9N is more common than type 9V in adults, and type 9V predominates in infants and children. In the United States there have been eight reported cases due to group 9 pneumococci in individuals previously vaccinated; six were type 9V and two were type 9N. To ascertain the cross-immunogenicity of group 9 polysaccharides, volunteers were injected with vaccines of monovalent types 9N, 9A, 9V, or 9L, or bivalent (9N and 9A) or trivalent (9N, 9A, and 9V) polysaccharide vaccines. Monovalent types 9N, 9V, and 9L each stimulated a 5.8- to 7.5-fold geometric mean rise, and at least 80% of the volunteers responded with a twofold or greater homologous antibody rise. Type 9V induced a 5.8-fold geometric mean rise, but only 66% of the volunteers responded with a twofold or greater homologous antibody rise. Type 9N induced only a 2.1-fold geometric increase, and only 54% of the volunteers responded with a twofold or greater rise in anti 9V antibodies. Types 9L and 9A were the most cross-immunogenic. The trivalent preparation (9N, 9A, and 9V) gave the highest geometric mean titer and seroconversion rate to each of the group 9 polysaccharides. These results suggest that the polyvalent pneumococcal vaccine with its type 9N does not induce a satisfactory anti-type 9V response and should contain additional components in order to achieve greater protection against group 9 organisms.

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Year:  1982        PMID: 7068216      PMCID: PMC351116          DOI: 10.1128/iai.35.3.777-782.1982

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.441


  15 in total

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Authors:  C V Broome; R R Facklam; J R Allen; D W Fraser; R Austrian
Journal:  J Infect Dis       Date:  1980-01       Impact factor: 5.226

2.  Impaired antibody response to pneumococcal vaccine after treatment for Hodgkin's disease.

Authors:  G R Siber; S A Weitzman; A C Aisenberg; H J Weinstein; G Schiffman
Journal:  N Engl J Med       Date:  1978-08-31       Impact factor: 91.245

3.  Structural studies of the capsular antigen from Streptococcus pneumoniae type 26.

Authors:  L Kenne; B Lindberg; J K Madden
Journal:  Carbohydr Res       Date:  1979-08       Impact factor: 2.104

4.  Types of pneumococci found in blood, spinal fluid and pleural exudate during a period of 15 years (1954-1969).

Authors:  E Lund
Journal:  Acta Pathol Microbiol Scand B Microbiol Immunol       Date:  1970

5.  Pneumococcal serotypes in West Africa.

Authors:  B M Greenwood; M Hassan-King; G Onyemelukwe; J T Macfarlane; H R Tubbs; P J Tugwell; H C Whittle; F Denis; J P Chiron; S M'boup; R Triau; M Cadoz; I D Mar
Journal:  Lancet       Date:  1980-02-16       Impact factor: 79.321

6.  Comparative immunogenicity of vaccines prepared from capsular polysaccharides of group C Neisseria meningitidis O-acetyl-positive and O-acetyl-negative variants and Escherichia coli K92 in adult volunteers.

Authors:  M P Glode; E B Lewin; A Sutton; C T Le; E C Gotschlich; J B Robbins
Journal:  J Infect Dis       Date:  1979-01       Impact factor: 5.226

7.  A radioimmunoassay for immunologic phenomena in pneumococcal disease and for the antibody response to pneumococcal vaccines. I. Method for the radioimmunoassay of anticapsular antibodies and comparison with other techniques.

Authors:  G Schiffman; R M Douglas; M J Bonner; M Robbins; R Austrian
Journal:  J Immunol Methods       Date:  1980       Impact factor: 2.303

8.  Characterization of the cross-reaction between type 19F(19) and 19A(57) pneumococcal capsular polysaccharides: compositional analysis and immunological relation determined with rabbit typing antisera.

Authors:  T Krishnamurthy; C J Lee; J Henrichsen; D J Carlo; T M Stoudt; J B Robbins
Journal:  Infect Immun       Date:  1978-12       Impact factor: 3.441

9.  Comparative immunogenicity of group 6 pneumococcal type 6A(6) and type 6B(26) capsular polysaccharides.

Authors:  J B Robbins; C J Lee; S C Rastogi; G Schiffman; J Henrichsen
Journal:  Infect Immun       Date:  1979-12       Impact factor: 3.441

10.  Form variation in Escherichia coli K1: determined by O-acetylation of the capsular polysaccharide.

Authors:  F Orskov; I Orskov; A Sutton; R Schneerson; W Lin; W Egan; G E Hoff; J B Robbins
Journal:  J Exp Med       Date:  1979-03-01       Impact factor: 14.307

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  6 in total

Review 1.  Immunogenicity and immunochemistry of Streptococcus pneumoniae capsular polysaccharides.

Authors:  J E van Dam; A Fleer; H Snippe
Journal:  Antonie Van Leeuwenhoek       Date:  1990-06       Impact factor: 2.271

2.  Seroepidemiologic characterization of Streptococcus pneumoniae in a Saudi hospital.

Authors:  S S Hussein; C C Anokute
Journal:  J Natl Med Assoc       Date:  1987-11       Impact factor: 1.798

3.  Serogroups and serotypes of pneumococci in Montreal: correlations with age, outcome and indications for vaccination.

Authors:  F Lamothe; G Delage; M Laverdière; P Saint-Antoine
Journal:  Can Med Assoc J       Date:  1984-03-15       Impact factor: 8.262

4.  Cross-reacting opsonic antibodies to clinically important pneumococcal serotypes after pneumococcal vaccination.

Authors:  J H Braconier; E B Myhre; H Odeberg
Journal:  Eur J Clin Microbiol       Date:  1983-10       Impact factor: 3.267

5.  Boosting humoral and cellular immunity to pneumococcus by vaccination before and just after autologous transplant for myeloma.

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6.  Antibody responses to capsular polysaccharide backbone and O-acetate side groups of Streptococcus pneumoniae type 9V in humans and rhesus macaques.

Authors:  T B McNeely; J M Staub; C M Rusk; M J Blum; J J Donnelly
Journal:  Infect Immun       Date:  1998-08       Impact factor: 3.441

  6 in total

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