Serologic response to pneumococcal vaccination in children experiencing recurrent invasive pneumococcal disease

Abstract Background Some children are prone to recurrent invasive pneumococcal disease (rIPD) and of these, some respond insufficiently to standard pneumococcal vaccination. Little is known about how to handle these children and if they benefit from additional vaccination. Here, we present results f...

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Main Authors: Helene A. S. Ingels, Bjørn Kantsø, Hans-Christian Slotved
Format: Article
Language:English
Published: BMC 2018-08-01
Series:BMC Infectious Diseases
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12879-018-3267-6
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author Helene A. S. Ingels
Bjørn Kantsø
Hans-Christian Slotved
author_facet Helene A. S. Ingels
Bjørn Kantsø
Hans-Christian Slotved
author_sort Helene A. S. Ingels
collection DOAJ
description Abstract Background Some children are prone to recurrent invasive pneumococcal disease (rIPD) and of these, some respond insufficiently to standard pneumococcal vaccination. Little is known about how to handle these children and if they benefit from additional vaccination. Here, we present results from a nationwide study of pediatric rIPD including data on serotype-specific vaccination response to pneumococcal polysaccharide vaccination (PPV23) and pneumococcal conjugate vaccination (PCV7/13). Methods A retrospective, population-based study was conducted using The National Streptococcus pneumoniae Registry, which contains laboratory-confirmed data from all cases of IPD in Denmark. From January 1980–June 2013 all children aged 0–15 years with rIPD were identified. Clinical data and data on serotype-specific pneumococcal antibody response were collected. Over the years quantification of pneumococcal antibodies varied from being presented in arbitrary units (ELISA), in μg/ml (WHO ELISA) and lately in μg/ml based on Luminex technology. Results 2482 children were diagnosed with IPD and 75 episodes of rIPD were documented in 59 children. An underlying disease was documented in 45 (76%) children. Vaccination data were available for 26 children; 11 were vaccinated solely with PPV23, 8 with a combination of PPV23 + PCV7, 5 with PCV7 and 2 with PCV13. In total, nine responded to PPV23 vaccination and ten were PPV23 non-responders. Of the 15 PCV vaccinated children, two children responded subnormal to PCV7. Among PPV23 non-responders, five responded to subsequent PCV vaccination. Conclusions In our population-based study of children with rIPD 53% of the children responded insufficiently to PPV23 vaccination. PPV23 non-responders benefitted from PCV vaccination.
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spelling doaj.art-729a2e7a8a5d4b9790605f3d9090e3112022-12-22T00:27:14ZengBMCBMC Infectious Diseases1471-23342018-08-011811710.1186/s12879-018-3267-6Serologic response to pneumococcal vaccination in children experiencing recurrent invasive pneumococcal diseaseHelene A. S. Ingels0Bjørn Kantsø1Hans-Christian Slotved2Department of Pediatrics, Slagelse HospitalDepartment of Microbiological Diagnostics &Virology, Statens Serum InstitutDepartment of Bacteria, Parasites and Fungi, Statens Serum InstitutAbstract Background Some children are prone to recurrent invasive pneumococcal disease (rIPD) and of these, some respond insufficiently to standard pneumococcal vaccination. Little is known about how to handle these children and if they benefit from additional vaccination. Here, we present results from a nationwide study of pediatric rIPD including data on serotype-specific vaccination response to pneumococcal polysaccharide vaccination (PPV23) and pneumococcal conjugate vaccination (PCV7/13). Methods A retrospective, population-based study was conducted using The National Streptococcus pneumoniae Registry, which contains laboratory-confirmed data from all cases of IPD in Denmark. From January 1980–June 2013 all children aged 0–15 years with rIPD were identified. Clinical data and data on serotype-specific pneumococcal antibody response were collected. Over the years quantification of pneumococcal antibodies varied from being presented in arbitrary units (ELISA), in μg/ml (WHO ELISA) and lately in μg/ml based on Luminex technology. Results 2482 children were diagnosed with IPD and 75 episodes of rIPD were documented in 59 children. An underlying disease was documented in 45 (76%) children. Vaccination data were available for 26 children; 11 were vaccinated solely with PPV23, 8 with a combination of PPV23 + PCV7, 5 with PCV7 and 2 with PCV13. In total, nine responded to PPV23 vaccination and ten were PPV23 non-responders. Of the 15 PCV vaccinated children, two children responded subnormal to PCV7. Among PPV23 non-responders, five responded to subsequent PCV vaccination. Conclusions In our population-based study of children with rIPD 53% of the children responded insufficiently to PPV23 vaccination. PPV23 non-responders benefitted from PCV vaccination.http://link.springer.com/article/10.1186/s12879-018-3267-6Streptococcus pneumoniaeVaccinationRecurrent diseaseNon-responderSerologyRecurrent IPD
spellingShingle Helene A. S. Ingels
Bjørn Kantsø
Hans-Christian Slotved
Serologic response to pneumococcal vaccination in children experiencing recurrent invasive pneumococcal disease
BMC Infectious Diseases
Streptococcus pneumoniae
Vaccination
Recurrent disease
Non-responder
Serology
Recurrent IPD
title Serologic response to pneumococcal vaccination in children experiencing recurrent invasive pneumococcal disease
title_full Serologic response to pneumococcal vaccination in children experiencing recurrent invasive pneumococcal disease
title_fullStr Serologic response to pneumococcal vaccination in children experiencing recurrent invasive pneumococcal disease
title_full_unstemmed Serologic response to pneumococcal vaccination in children experiencing recurrent invasive pneumococcal disease
title_short Serologic response to pneumococcal vaccination in children experiencing recurrent invasive pneumococcal disease
title_sort serologic response to pneumococcal vaccination in children experiencing recurrent invasive pneumococcal disease
topic Streptococcus pneumoniae
Vaccination
Recurrent disease
Non-responder
Serology
Recurrent IPD
url http://link.springer.com/article/10.1186/s12879-018-3267-6
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AT hanschristianslotved serologicresponsetopneumococcalvaccinationinchildrenexperiencingrecurrentinvasivepneumococcaldisease