Evidence map›Paper›PMID 40711589›Full record

ArticleEuropean journal of pediatrics2025

Impact of pertussis vaccination on PT-IgG levels and clinical characteristics in 3-12-month-old infants with acute pertussis.

Yuanyuan Wu, Chuan Gan

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Article in European journal of pediatrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1 · What the graph read from it

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1 citing paper in PubMed.

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5 · Who and what money

Authors and funding

2 authors.

Yuanyuan WuHealth Medicine Center, The Second Affiliated Hospital of Chongqing Medical University, Chongqing Medical University, Chongqing, China.
Chuan GanDepartment of Infectious Diseases, National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Child Rare Diseases in Infection and Immunity, The First Batch of Key Disciplines On Public Health in Chongqing, Children's Hospital of Chongqing Medical University, No. 136 Zhongshaner Road, Yuzhong District, Chongqing, 400014, China. 481984@hospital.cqmu.edu.cn.

Funding

Natural Science Foundation of China No. 82401838Natural Science Foundation of Chongqing CSTB2023NSCQ-BHX0042
6 · The paper itself

Abstract

Although some studies have explored changes in PT-IgG levels following vaccination or Bordetella pertussis infection, the relationship between PT-IgG levels and clinical characteristics in patients with acute-phase pertussis remains unclear. We retrospectively analyzed clinical data from 333 infants aged 3-12 months hospitalized with acute pertussis at the Children's Hospital of Chongqing Medical University between April 1, 2018, and July 31, 2019. Patients were stratified into vaccinated and unvaccinated groups based on their immunization records. We evaluated differences in clinical manifestations, complications, laboratory findings, and dynamics of PT-IgG antibody. The median age of disease onset was 137.5 days for unvaccinated patients and 163 days for vaccinated patients. PT-IgG levels were significantly higher in the vaccinated group (19.25 [1.58, 59.18] IU/mL) compared to the unvaccinated group (2.43 [0.05, 24.01] IU/mL; P < 0.001). Unvaccinated patients exhibited higher incidences of peak white blood cell (WBC) counts in the range of 20-30 × 10⁹/L, 30-50 × 10⁹/L, and > 50 × 10⁹/L (P = 0.031). Vaccinated patients demonstrated a rapid elevation of PT-IgG, peaking at week 5 post-infection (52.08 IU/mL), while unvaccinated patients showed delayed antibody production, with levels rising significantly only by week 6 (26.99 IU/mL). Although clinical symptoms and complications did not differ significantly between the groups, unvaccinated patients had higher rates of severe indicators.

conclusionVaccination against pertussis accelerates PT-IgG production in infants aged 3-12 months. Unvaccinated patients experience delayed antibody responses, lower PT-IgG levels, and increased risks of severe complications. These findings emphasize the critical role of vaccination in mitigating pertussis-related morbidity.

conclusionTwo-thirds of outpatients were non-adherent to anti-infectives in acute infectious diseases. WHAT IS KNOWN: • Pertussis vaccination influences PT-IgG levels following Bordetella pertussis infection and affects disease severity. WHAT IS NEW: • To our knowledge, this study represents the first large-scale analysis of the impact of pertussis vaccination on antibody kinetic changes during the initial 6 weeks post-Bordetella pertussis infection. • Unvaccinated patients exhibited delayed antibody production and lower peak antibody titers, resulting in a higher probability of severe clinical manifestations. Particular clinical attention should be given to pertussis-unvaccinated patients.

Indexed as

Antibodies, BacterialBordetella pertussisImmunoglobulin GPertussis VaccineVaccinationWhooping CoughAcute DiseaseFemaleHumansInfantMaleRetrospective StudiesAntibodies, BacterialImmunoglobulin GPertussis VaccineAcuteInfantPertussisPT-IgGVaccination

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.