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Int J Infect Dis. 1999 Spring;3(3):140-6.

Parapertussis and pertussis: differences and similarities in incidence, clinical course, and antibody responses.

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1
The Göteborg Pertussis Vaccine Trial, the Göteborg Primary Health Care System, Göteborg, Sweden.

Abstract

OBJECTIVES:

To compare the incidence, clinical course, and serologic response to Bordetella antigens in patients with parapertussis and pertussis.

DESIGN:

Two studies were performed in Sweden during the 1990s, when pertussis vaccines were used only in clinical trials. Study I was a retrospective study of patients with positive Bordetella cultures obtained in clinical routine, and study II involved an active search for patients with Bordetella infections during a placebo-controlled trial of a pertussis toxoid vaccine.

RESULTS:

Study I includes 58, and study II 23 patients with parapertussis. In study I, the incidence of parapertussis was 0.016 cases per 100 person years in children 0 to 6 years old and 0 in older children and adults. In study II, the incidence rates of parapertussis and pertussis were 0.2 and 16.2 per 100 person years, respectively, in children followed from 3 months to 3 years of age. The median number of days with cough was 21 in parapertussis and 59 in pertussis. The proportions of children with whooping and vomiting were lower in parapertussis than in pertussis. Geometric mean serum filamentous hemagglutinin IgG increased from 6 to 63, and pertactin IgG from 4 to 12 units/mL in parapertussis patients, which was similar to increases in children with pertussis.

CONCLUSIONS:

Disease caused by Bordetella parapertussis is diagnosed less commonly and is milder and of shorter duration than disease caused by Bordetella pertussis. Parapertussis induced serum IgG against filamentous hemagglutinin and pertactin of similar magnitude as does pertussis, and did not induce serum IgG against pertussis toxin.

PMID:
10460925
[Indexed for MEDLINE]
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