Association between pertussis vaccination in infancy and childhood asthma: A population-based record linkage cohort

Gladymar Pérez Chacón1,2, Parveen Fathima1,3, Mark Jones3

  • 1Wesfarmers Centre of Vaccines and Infectious Diseases, Telethon Kids Institute, University of Western Australia, Perth, Western Australia, Australia.

Plos One
|October 4, 2023
PubMed

Insights

Whole-cell pertussis (wP) vaccines given in infancy did not show a protective effect against childhood asthma hospitalizations. This large study found no significant difference in asthma risk between wP and acellular pertussis (aP) vaccine recipients.

Area of Science:

  • Pediatric Allergy and Immunology
  • Vaccinology
  • Epidemiology

Background:

  • Asthma is a common childhood noncommunicable disease often co-occurring with atopic conditions.
  • Prior research suggested whole-cell pertussis (wP) vaccines might reduce IgE-mediated food allergy risk compared to acellular pertussis (aP) vaccines.
  • This led to the hypothesis that wP vaccination could protect against childhood atopic asthma.

Purpose of the Study:

  • To investigate the potential protective association between early infancy whole-cell pertussis (wP) vaccination and the risk of atopic asthma in childhood.
  • To compare asthma hospitalization rates in children who received wP versus aP vaccines as their first pertussis dose.

Main Methods:

  • A retrospective record-linkage cohort study included over 274,000 children born between 1997 and 1999 in Australia.
  • Children received either wP or aP vaccine as their primary pertussis immunization.
  • Asthma hospitalizations (first and recurrent) were the primary outcomes, analyzed using Cox and Andersen and Gill models to compute hazard ratios (HRs).

Main Results:

  • The study analyzed 274,405 children, with 5,905 asthma hospitalizations recorded.
  • Incidence rates for first asthma hospitalization were similar between wP (1.5/1000 child-years) and aP (1.5/1000 child-years) vaccine groups.
  • Adjusted HRs showed no significant difference: 1.02 (95% CI 0.94-1.12) for first hospitalizations and 1.07 (95% CI 0.95-1.2) for recurrent hospitalizations for wP versus aP.

Conclusions:

  • No convincing clinical evidence supports an association between early infancy wP vaccination and reduced hospital presentations for childhood asthma.
  • The findings do not support a protective role of wP vaccines against atopic asthma in childhood.
  • Further research may be needed to explore other potential long-term effects of different pertussis vaccine types.
Abstract

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