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Clinical Characteristics of Children With Celiac Disease Not Responding to Hepatitis B Vaccination in India
The immunological response to hepatitis B virus (HBV) vaccine may be suboptimal in children with celiac disease (CD), but the reasons for this are not well defined. OBJECTIVES: This study was undertaken to assess the immune response to HBV vaccine in CD children and to explore the possible factors a...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins, Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10191543/ https://www.ncbi.nlm.nih.gov/pubmed/37206938 http://dx.doi.org/10.1097/PG9.0000000000000046 |
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author | Aneja, Aradhana Lal, Sadhna B. Sharma, Arun K Rawat, Amit Singh, Surjit |
author_facet | Aneja, Aradhana Lal, Sadhna B. Sharma, Arun K Rawat, Amit Singh, Surjit |
author_sort | Aneja, Aradhana |
collection | PubMed |
description | The immunological response to hepatitis B virus (HBV) vaccine may be suboptimal in children with celiac disease (CD), but the reasons for this are not well defined. OBJECTIVES: This study was undertaken to assess the immune response to HBV vaccine in CD children and to explore the possible factors affecting the immune response. METHODS: The study population consisted of 3 groups—50 newly diagnosed CD children (group 1), 50 previously diagnosed CD children who were on gluten free diet (GFD) >3 months (group 2), and 100 age and gender matched healthy controls (group 3). The patient characteristics were recorded, and the blood samples were analyzed for HBsAg and anti-HBs titers. The nonresponders were given a booster dose of HBV vaccine and reevaluated after 6 weeks. RESULTS: Positive anti-HBs response was found in 46% in newly diagnosed CD children, 60% in CD children on GFD, and 83% in healthy controls (P < 0.001). The immune response to HBV vaccine in CD children was inferior to that in healthy children (53% vs 83%, P < 0.001). The immune response was found to be significantly affected by age at diagnosis, delay in diagnosis, type of presentation, and compliance to GFD. 44 out of 45 (97.77%) nonresponders from CD group seroconverted after a single booster dose. CONCLUSION: Early diagnosis and good compliance to GFD may improve the immune response to HBV vaccine in CD children. Single additional booster dose is sufficient to attain optimal immune response. |
format | Online Article Text |
id | pubmed-10191543 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Lippincott Williams & Wilkins, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101915432023-05-18 Clinical Characteristics of Children With Celiac Disease Not Responding to Hepatitis B Vaccination in India Aneja, Aradhana Lal, Sadhna B. Sharma, Arun K Rawat, Amit Singh, Surjit JPGN Rep Original Article The immunological response to hepatitis B virus (HBV) vaccine may be suboptimal in children with celiac disease (CD), but the reasons for this are not well defined. OBJECTIVES: This study was undertaken to assess the immune response to HBV vaccine in CD children and to explore the possible factors affecting the immune response. METHODS: The study population consisted of 3 groups—50 newly diagnosed CD children (group 1), 50 previously diagnosed CD children who were on gluten free diet (GFD) >3 months (group 2), and 100 age and gender matched healthy controls (group 3). The patient characteristics were recorded, and the blood samples were analyzed for HBsAg and anti-HBs titers. The nonresponders were given a booster dose of HBV vaccine and reevaluated after 6 weeks. RESULTS: Positive anti-HBs response was found in 46% in newly diagnosed CD children, 60% in CD children on GFD, and 83% in healthy controls (P < 0.001). The immune response to HBV vaccine in CD children was inferior to that in healthy children (53% vs 83%, P < 0.001). The immune response was found to be significantly affected by age at diagnosis, delay in diagnosis, type of presentation, and compliance to GFD. 44 out of 45 (97.77%) nonresponders from CD group seroconverted after a single booster dose. CONCLUSION: Early diagnosis and good compliance to GFD may improve the immune response to HBV vaccine in CD children. Single additional booster dose is sufficient to attain optimal immune response. Lippincott Williams & Wilkins, Inc. 2021-01-13 /pmc/articles/PMC10191543/ /pubmed/37206938 http://dx.doi.org/10.1097/PG9.0000000000000046 Text en Copyright © 2021 The Author(s). Published by Wolters Kluwer on behalf of European Society for Pediatric Gastroenterology, Hepatology, and Nutrition and North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Aneja, Aradhana Lal, Sadhna B. Sharma, Arun K Rawat, Amit Singh, Surjit Clinical Characteristics of Children With Celiac Disease Not Responding to Hepatitis B Vaccination in India |
title | Clinical Characteristics of Children With Celiac Disease Not Responding to Hepatitis B Vaccination in India |
title_full | Clinical Characteristics of Children With Celiac Disease Not Responding to Hepatitis B Vaccination in India |
title_fullStr | Clinical Characteristics of Children With Celiac Disease Not Responding to Hepatitis B Vaccination in India |
title_full_unstemmed | Clinical Characteristics of Children With Celiac Disease Not Responding to Hepatitis B Vaccination in India |
title_short | Clinical Characteristics of Children With Celiac Disease Not Responding to Hepatitis B Vaccination in India |
title_sort | clinical characteristics of children with celiac disease not responding to hepatitis b vaccination in india |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10191543/ https://www.ncbi.nlm.nih.gov/pubmed/37206938 http://dx.doi.org/10.1097/PG9.0000000000000046 |
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