Cargando…
Celiac disease and complement activation in response to Streptococcus pneumoniae
Individuals with celiac disease (CD) are at increased risk of invasive pneumococcal disease (IPD). The aim of this study was to explore whether the complement response to Streptococcus pneumoniae differed according to CD status, and could serve as an explanation for the excess risk of IPD in CD. Twe...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6942560/ https://www.ncbi.nlm.nih.gov/pubmed/31691001 http://dx.doi.org/10.1007/s00431-019-03490-w |
_version_ | 1783484729428803584 |
---|---|
author | Tjernberg, Anna Röckert Woksepp, Hanna Sandholm, Kerstin Johansson, Marcus Dahle, Charlotte Ludvigsson, Jonas F Bonnedahl, Jonas Nilsson, Per Ekdahl, Kristina Nilsson |
author_facet | Tjernberg, Anna Röckert Woksepp, Hanna Sandholm, Kerstin Johansson, Marcus Dahle, Charlotte Ludvigsson, Jonas F Bonnedahl, Jonas Nilsson, Per Ekdahl, Kristina Nilsson |
author_sort | Tjernberg, Anna Röckert |
collection | PubMed |
description | Individuals with celiac disease (CD) are at increased risk of invasive pneumococcal disease (IPD). The aim of this study was to explore whether the complement response to Streptococcus pneumoniae differed according to CD status, and could serve as an explanation for the excess risk of IPD in CD. Twenty-two children with CD and 18 controls, born 1999–2008, were included at Kalmar County Hospital, Sweden. The degree of complement activation was evaluated by comparing levels of activation products C3a and sC5b-9 in plasma incubated for 30 min with Streptococcus pneumoniae and in non-incubated plasma. Complement analyses were performed with enzyme-linked immunosorbent assay (ELISA). Pneumococcal stimulation caused a statistically significant increase in C3a as well as sC5b-9 in both children with CD and controls but there was no difference in response between the groups. After incubation, C3a increased on average 4.6 times and sC5b-9 22 times in both the CD and the control group (p = 0.497 and p = 0.724 respectively). Conclusion: Complement response to Streptococcus pneumoniae seems to be similar in children with and without CD and is thus unlikely to contribute to the increased susceptibility to invasive pneumococcal disease in CD. |
format | Online Article Text |
id | pubmed-6942560 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-69425602020-01-16 Celiac disease and complement activation in response to Streptococcus pneumoniae Tjernberg, Anna Röckert Woksepp, Hanna Sandholm, Kerstin Johansson, Marcus Dahle, Charlotte Ludvigsson, Jonas F Bonnedahl, Jonas Nilsson, Per Ekdahl, Kristina Nilsson Eur J Pediatr Original Article Individuals with celiac disease (CD) are at increased risk of invasive pneumococcal disease (IPD). The aim of this study was to explore whether the complement response to Streptococcus pneumoniae differed according to CD status, and could serve as an explanation for the excess risk of IPD in CD. Twenty-two children with CD and 18 controls, born 1999–2008, were included at Kalmar County Hospital, Sweden. The degree of complement activation was evaluated by comparing levels of activation products C3a and sC5b-9 in plasma incubated for 30 min with Streptococcus pneumoniae and in non-incubated plasma. Complement analyses were performed with enzyme-linked immunosorbent assay (ELISA). Pneumococcal stimulation caused a statistically significant increase in C3a as well as sC5b-9 in both children with CD and controls but there was no difference in response between the groups. After incubation, C3a increased on average 4.6 times and sC5b-9 22 times in both the CD and the control group (p = 0.497 and p = 0.724 respectively). Conclusion: Complement response to Streptococcus pneumoniae seems to be similar in children with and without CD and is thus unlikely to contribute to the increased susceptibility to invasive pneumococcal disease in CD. Springer Berlin Heidelberg 2019-11-05 2020 /pmc/articles/PMC6942560/ /pubmed/31691001 http://dx.doi.org/10.1007/s00431-019-03490-w Text en © The Author(s) 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Article Tjernberg, Anna Röckert Woksepp, Hanna Sandholm, Kerstin Johansson, Marcus Dahle, Charlotte Ludvigsson, Jonas F Bonnedahl, Jonas Nilsson, Per Ekdahl, Kristina Nilsson Celiac disease and complement activation in response to Streptococcus pneumoniae |
title | Celiac disease and complement activation in response to Streptococcus pneumoniae |
title_full | Celiac disease and complement activation in response to Streptococcus pneumoniae |
title_fullStr | Celiac disease and complement activation in response to Streptococcus pneumoniae |
title_full_unstemmed | Celiac disease and complement activation in response to Streptococcus pneumoniae |
title_short | Celiac disease and complement activation in response to Streptococcus pneumoniae |
title_sort | celiac disease and complement activation in response to streptococcus pneumoniae |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6942560/ https://www.ncbi.nlm.nih.gov/pubmed/31691001 http://dx.doi.org/10.1007/s00431-019-03490-w |
work_keys_str_mv | AT tjernbergannarockert celiacdiseaseandcomplementactivationinresponsetostreptococcuspneumoniae AT woksepphanna celiacdiseaseandcomplementactivationinresponsetostreptococcuspneumoniae AT sandholmkerstin celiacdiseaseandcomplementactivationinresponsetostreptococcuspneumoniae AT johanssonmarcus celiacdiseaseandcomplementactivationinresponsetostreptococcuspneumoniae AT dahlecharlotte celiacdiseaseandcomplementactivationinresponsetostreptococcuspneumoniae AT ludvigssonjonasf celiacdiseaseandcomplementactivationinresponsetostreptococcuspneumoniae AT bonnedahljonas celiacdiseaseandcomplementactivationinresponsetostreptococcuspneumoniae AT nilssonper celiacdiseaseandcomplementactivationinresponsetostreptococcuspneumoniae AT ekdahlkristinanilsson celiacdiseaseandcomplementactivationinresponsetostreptococcuspneumoniae |