Evidence map›Paper›PMID 39387142›Full record

ArticleClinical and experimental immunology2025

Pneumococcal serotype-specific antibodies in children with recurrent oto-sinopulmonary infections.

Hanadys Ale, Jose G Calderon, Joshua Gruber, Thomas Taylor, William R Blouin, Vivian P Hernández-Trujillo

Abstract read
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Article in Clinical and experimental immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Hanadys AleDivision of Immunology, Allergy, and Rheumatology, Joe DiMaggio Children's Hospital, Hollywood, FL, USA.ORCID 0009-0008-4583-1808
Jose G CalderonDivision of Allergy & Immunology, Nicklaus Children's Hospital, Miami, FL, USA.
Joshua GruberNicklaus Children's Hospital Research Institute, Miami, FL, USA.
Thomas TaylorNicklaus Children's Hospital Research Institute, Miami, FL, USA.
William R BlouinDivision of Allergy & Immunology, Nicklaus Children's Hospital, Miami, FL, USA.
Vivian P Hernández-TrujilloDivision of Allergy & Immunology, Nicklaus Children's Hospital, Miami, FL, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Low titers to pneumococcal vaccine are a frequent finding in pediatric patients with recurrent oto-sinopulmonary infections. To characterize the pre- and post-immunization antibody trend for each serotype included in the pneumococcal 13-valent conjugate vaccine, in a cohort of pediatric patients with recurrent oto-sinopulmonary infections, this retrospective review identified 182 patients with recurrent oto-sinopulmonary infections (131 required an immune workup and 99 had low pneumococcal titers leading to a pneumococcal 13-valent conjugate vaccine booster). Baseline pneumococcal serotype-specific antibody titers at the initial visit and 6 weeks after the vaccine booster were obtained. An adequate response to the pneumococcal conjugate vaccine was deemed to be a 4-fold increase over baseline and/or a post-immunization titer of 1.3 µg/ml or greater. Overall, The pneumococcal 13-valent conjugate vaccine booster provided a significant improvement in the number of protective titers, increasing from 3.6 serotypes at baseline to 11.1 serotypes at 6 weeks (P < 0.001). This increase correlated with improved clinical outcomes (81% showed no signs of recurrent infection after the first booster and 94% after a second booster). Post-immunization antibody concentrations were significantly higher than at baseline for all serotypes (P < 0.05), and only 8, 9N, and 12F did not exhibit a greater than 4-fold increase (P > 0.05) 6 weeks following booster. There were no differences between patients at different ages in post-immunization titer levels for all serotypes. In pediatric patients with recurrent oto-sinopulmonary infections, an additional pneumococcal booster proved to be effective in the protection of these children against further infections, across all age groups.

Indexed as

Antibodies, BacterialPneumococcal InfectionsPneumococcal VaccinesRespiratory Tract InfectionsStreptococcus pneumoniaeAdolescentChildChild, PreschoolFemaleHumansImmunization, SecondaryInfantMaleRecurrenceRetrospective StudiesSerogroup13-valent pneumococcal vaccineAntibodies, BacterialPneumococcal VaccinesVaccines, Conjugateantibodiesinfectionvaccine

Identifiers

PMID39387142
PMCPMC11771189

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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.