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Does early EBV infection protect against IgE sensitization?
BACKGROUND: There is indirect evidence that an increased infectious burden is associated with a decreased prevalence of IgE-mediated allergy during childhood. OBJECTIVE: To determine whether there is a relation between the serostatus of 13 different viruses and parentally reported infections and IgE...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Academy of Allergy, Asthma and Immunology. Published by Mosby, Inc.
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7119037/ https://www.ncbi.nlm.nih.gov/pubmed/16083803 http://dx.doi.org/10.1016/j.jaci.2005.04.027 |
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author | Nilsson, Caroline Linde, Annika Montgomery, Scott M. Gustafsson, Liselotte Näsman, Per Blomberg, Marita Troye Lilja, Gunnar |
author_facet | Nilsson, Caroline Linde, Annika Montgomery, Scott M. Gustafsson, Liselotte Näsman, Per Blomberg, Marita Troye Lilja, Gunnar |
author_sort | Nilsson, Caroline |
collection | PubMed |
description | BACKGROUND: There is indirect evidence that an increased infectious burden is associated with a decreased prevalence of IgE-mediated allergy during childhood. OBJECTIVE: To determine whether there is a relation between the serostatus of 13 different viruses and parentally reported infections and IgE sensitization in 2-year-old children. To investigate whether there is an interaction between cytomegalovirus (CMV) and Epstein-Barr virus (EBV) in relation to IgE sensitization. METHODS: A total of 246 infants were followed prospectively to 2 years of age with clinical examinations, skin prick test, and specific IgE analyses and through analysis of seropositivity against adenovirus, influenza, parainfluenza, respiratory syncytial virus, CMV, EBV, herpes simplex virus, human herpesvirus 6, and varicella-zoster virus. RESULTS: There was some evidence that IgE sensitization (24%) tended to be more common among children who were seropositive against few compared with children who were seropositive against many viruses, but this was not statistically significant, and there was no consistent trend across the groups. IgE sensitization was statistically significantly less prevalent at 2 years of age among infants who were seropositive against EBV but not other viruses (adjusted odds ratio, 0.34; 95% CI, 0.14-0.86). The interaction of seropositivity against both CMV and EBV antibodies indicated a further reduction in the risk for IgE sensitization (adjusted odds ratio for interaction, 0.10; 95% CI, 0.01-0.92), indicating effect modification associated with seropositivity against CMV. CONCLUSION: Our results indicate that acquisition of EBV infection during the first 2 years of life is associated with a reduced risk of IgE sensitization, and this effect is enhanced by CMV coinfection. |
format | Online Article Text |
id | pubmed-7119037 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | American Academy of Allergy, Asthma and Immunology. Published by Mosby, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71190372020-04-03 Does early EBV infection protect against IgE sensitization? Nilsson, Caroline Linde, Annika Montgomery, Scott M. Gustafsson, Liselotte Näsman, Per Blomberg, Marita Troye Lilja, Gunnar J Allergy Clin Immunol Basic and Clinical Immunology BACKGROUND: There is indirect evidence that an increased infectious burden is associated with a decreased prevalence of IgE-mediated allergy during childhood. OBJECTIVE: To determine whether there is a relation between the serostatus of 13 different viruses and parentally reported infections and IgE sensitization in 2-year-old children. To investigate whether there is an interaction between cytomegalovirus (CMV) and Epstein-Barr virus (EBV) in relation to IgE sensitization. METHODS: A total of 246 infants were followed prospectively to 2 years of age with clinical examinations, skin prick test, and specific IgE analyses and through analysis of seropositivity against adenovirus, influenza, parainfluenza, respiratory syncytial virus, CMV, EBV, herpes simplex virus, human herpesvirus 6, and varicella-zoster virus. RESULTS: There was some evidence that IgE sensitization (24%) tended to be more common among children who were seropositive against few compared with children who were seropositive against many viruses, but this was not statistically significant, and there was no consistent trend across the groups. IgE sensitization was statistically significantly less prevalent at 2 years of age among infants who were seropositive against EBV but not other viruses (adjusted odds ratio, 0.34; 95% CI, 0.14-0.86). The interaction of seropositivity against both CMV and EBV antibodies indicated a further reduction in the risk for IgE sensitization (adjusted odds ratio for interaction, 0.10; 95% CI, 0.01-0.92), indicating effect modification associated with seropositivity against CMV. CONCLUSION: Our results indicate that acquisition of EBV infection during the first 2 years of life is associated with a reduced risk of IgE sensitization, and this effect is enhanced by CMV coinfection. American Academy of Allergy, Asthma and Immunology. Published by Mosby, Inc. 2005-08 2005-07-05 /pmc/articles/PMC7119037/ /pubmed/16083803 http://dx.doi.org/10.1016/j.jaci.2005.04.027 Text en Copyright © 2005 American Academy of Allergy, Asthma and Immunology. Published by Mosby, Inc. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Basic and Clinical Immunology Nilsson, Caroline Linde, Annika Montgomery, Scott M. Gustafsson, Liselotte Näsman, Per Blomberg, Marita Troye Lilja, Gunnar Does early EBV infection protect against IgE sensitization? |
title | Does early EBV infection protect against IgE sensitization? |
title_full | Does early EBV infection protect against IgE sensitization? |
title_fullStr | Does early EBV infection protect against IgE sensitization? |
title_full_unstemmed | Does early EBV infection protect against IgE sensitization? |
title_short | Does early EBV infection protect against IgE sensitization? |
title_sort | does early ebv infection protect against ige sensitization? |
topic | Basic and Clinical Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7119037/ https://www.ncbi.nlm.nih.gov/pubmed/16083803 http://dx.doi.org/10.1016/j.jaci.2005.04.027 |
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