Literature DB >> 2759713

Immunoglobulin E response to pertussis toxin in whooping cough and after immunization with a whole-cell and an acellular pertussis vaccine.

S Hedenskog1, B Björkstén, M Blennow, G Granström, M Granström.   

Abstract

Immunoglobulin E antibodies to pertussis toxin (PT-IgE) were demonstrated in 15 of 23 (65%) patients with culture-confirmed pertussis. In 6 individuals there was a low-grade PT-IgE response after 6-9 weeks of disease and in 9 a rapid PT-IgE response, appearing 1-3 weeks after onset of symptoms. The PT-IgE antibody levels in immunized individuals were higher than in the non immunized. Following primary immunization of 23 children with a monovalent whole-cell pertussis vaccine (Burroughs-Wellcome, UK) or with an acellular pertussis vaccine (JNIH-6, Biken, Japan) a late low-grade PT-IgE response was found in 8 (35%). In 7/10 children previously immunized with the JNIH-6, a booster injection 16 months later with the same vaccine resulted in a rapidly appearing PT-IgE antibody response. In contrast, none of 13 children initially immunized with the monovalent whole-cell vaccine and then boostered with either this vaccine or JNIH-6 had detectable PT-IgE antibodies after the booster injection. The study shows that IgE-antibodies to pertussis toxin commonly appear in patients with whooping cough and that the kinetics and the magnitude of the response is influenced by previous exposure to the antigen. A PT-IgE response may also follow pertussis immunization.

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Year:  1989        PMID: 2759713     DOI: 10.1159/000234939

Source DB:  PubMed          Journal:  Int Arch Allergy Appl Immunol        ISSN: 0020-5915


  13 in total

1.  Booster immunization of children with an acellular pertussis vaccine enhances Th2 cytokine production and serum IgE responses against pertussis toxin but not against common allergens.

Authors:  E J Ryan; L Nilsson; N Kjellman; L Gothefors; K H Mills
Journal:  Clin Exp Immunol       Date:  2000-08       Impact factor: 4.330

Review 2.  Environmental risk factors for atopy.

Authors:  B Björkstén
Journal:  Clin Rev Allergy Immunol       Date:  1997       Impact factor: 8.667

3.  Co-stimulation of T cells via CD28 inhibits human IgE production; reversal by pertussis toxin.

Authors:  C T Van der Pouw-Kraan; H J Rensink; R Rappuoli; L A Aarden
Journal:  Clin Exp Immunol       Date:  1995-03       Impact factor: 4.330

4.  Lymphokine secretion and cytotoxic activity of human CD4+ T-cell clones against Bordetella pertussis.

Authors:  S Peppoloni; L Nencioni; A Di Tommaso; A Tagliabue; P Parronchi; S Romagnani; R Rappuoli; M T De Magistris
Journal:  Infect Immun       Date:  1991-10       Impact factor: 3.441

Review 5.  Acellular pertussis vaccine safety and efficacy in children, adolescents and adults.

Authors:  Janet R Casey; Michael E Pichichero
Journal:  Drugs       Date:  2005       Impact factor: 9.546

6.  Differences in coughing and other responses to intrabronchial infection with Bordetella pertussis among strains of rats.

Authors:  E Hall; R Parton; A C Wardlaw
Journal:  Infect Immun       Date:  1997-11       Impact factor: 3.441

7.  Acellular pertussis vaccine protects against exacerbation of allergic asthma due to Bordetella pertussis in a murine model.

Authors:  Darren P Ennis; Joseph P Cassidy; Bernard P Mahon
Journal:  Clin Diagn Lab Immunol       Date:  2005-03

8.  Does pertussis infection induce manifestation of allergy?

Authors:  A Schuster; A Hofmann; D Reinhardt
Journal:  Clin Investig       Date:  1993-03

Review 9.  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

10.  Enhancement of interleukin-4 production by pertussis toxin.

Authors:  H H Mu; W A Sewell
Journal:  Infect Immun       Date:  1993-07       Impact factor: 3.441

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