Literature DB >> 8515102

Acellular pertussis vaccines--a solution to the pertussis problem?

K M Edwards1.   

Abstract

The expanded knowledge of the components of Bordetella pertussis has led to the production of new vaccines consisting of one or more components of the organism. The vaccines have been found to be safe and immunogenic in infants and children. Early efficacy studies failed to determine what component of the vaccine and what level of antibody were needed for protection; additional studies with many more vaccines are currently in progress. The role of adults as reservoirs of B. pertussis infections and as victims of symptomatic disease has also been appreciated. Component vaccines have been found to be safe and immunogenic in adults. There is reason to hope that within the next several years the information derived from ongoing and planned studies will support the general use of component acellular pertussis vaccines for the routine immunization of adults and children alike.

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Year:  1993        PMID: 8515102     DOI: 10.1093/infdis/168.1.15

Source DB:  PubMed          Journal:  J Infect Dis        ISSN: 0022-1899            Impact factor:   5.226


  10 in total

1.  Mechanisms of pertussis toxin-induced myelomonocytic cell adhesion: role of CD14 and urokinase receptor.

Authors:  H Li; W S Wong
Journal:  Immunology       Date:  2000-08       Impact factor: 7.397

Review 2.  Diphtheria-tetanus-acellular pertussis vaccine adsorbed (Triacelluvax; DTaP3-CB): a review of its use in the prevention of Bordetella pertussis infection.

Authors:  A J Matheson; K L Goa
Journal:  Paediatr Drugs       Date:  2000 Mar-Apr       Impact factor: 3.022

Review 3.  Acellular pertussis vaccines.

Authors:  E Miller
Journal:  Arch Dis Child       Date:  1995-11       Impact factor: 3.791

Review 4.  The family of bacterial ADP-ribosylating exotoxins.

Authors:  K M Krueger; J T Barbieri
Journal:  Clin Microbiol Rev       Date:  1995-01       Impact factor: 26.132

5.  Pertussis toxin activates platelets through an interaction with platelet glycoprotein Ib.

Authors:  K A Sindt; E L Hewlett; G T Redpath; R Rappuoli; L S Gray; S R Vandenberg
Journal:  Infect Immun       Date:  1994-08       Impact factor: 3.441

6.  Characterization of a recombinant fragment that contains a carbohydrate recognition domain of the filamentous hemagglutinin.

Authors:  D F Liu; E Phillips; T M Wizemann; M M Siegel; K Tabei; J L Cowell; E Tuomanen
Journal:  Infect Immun       Date:  1997-08       Impact factor: 3.441

Review 7.  A cellular pertussis vaccine (Infanrix-DTPa; SB-3). A review of its immunogenicity, protective efficacy and tolerability in the prevention of Bordetella pertussis infection.

Authors:  S S Patel; A J Wagstaff
Journal:  Drugs       Date:  1996-08       Impact factor: 9.546

8.  Serum antibodies to the components of diphtheria-tetanus-pertussis vaccine in Polish children related to vaccination status.

Authors:  E Torbicka; T Lagergård; B Trollfors
Journal:  Infection       Date:  1995 Jul-Aug       Impact factor: 3.553

9.  Human antibody response to the B oligomer of pertussis toxin.

Authors:  F Lynn; W N Burnette; G R Siber; J L Arciniega
Journal:  Clin Diagn Lab Immunol       Date:  1994-11

10.  Antigenic analysis of Bordetella pertussis filamentous hemagglutinin with phage display libraries and rabbit anti-filamentous hemagglutinin polyclonal antibodies.

Authors:  D R Wilson; A Siebers; B B Finlay
Journal:  Infect Immun       Date:  1998-10       Impact factor: 3.441

  10 in total

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