Heterogeneous associations of polyomaviruses and herpesviruses with allergy-related phenotypes in childhood.


Journal

Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology
ISSN: 1534-4436
Titre abrégé: Ann Allergy Asthma Immunol
Pays: United States
ID NLM: 9503580

Informations de publication

Date de publication:
08 2021
Historique:
received: 08 02 2021
revised: 12 04 2021
accepted: 16 04 2021
pubmed: 26 4 2021
medline: 15 9 2021
entrez: 25 4 2021
Statut: ppublish

Résumé

Evidence suggests a complex interplay between infections and allergic diseases. To explore the association of 14 common viruses with eczema, asthma, and rhinoconjunctivitis in childhood. We used cross-sectional (n = 686) and prospective (n = 440) data from children participating in the Rhea birth cohort. Immunoglobulin G to polyomaviruses (BK polyomavirus, JC polyomavirus, KI polyomavirus [KIPyV], WU polyomavirus [WUPyV], human polyomavirus 6, human polyomavirus 7, Trichodysplasia spinulosa polyomavirus, Merkel cell polyomavirus, human polyomavirus 9, and human polyomavirus 10) and herpesviruses (Epstein-Barr virus, Cytomegalovirus, Herpes simplex virus-1, Herpes simplex virus-2) were measured at age 4 years by fluorescent bead-based multiplex serology. Definitions of eczema, asthma, and rhinoconjunctivitis at ages 4 and 6 years were based on questionnaires. Mediation of the associations by immune biomarkers was tested. Less likely to have eczema at age 4 years were KIPyV-seropositive (odds ratio [OR], 0.47; 95% confidence interval [CI], 0.27-0.82) and human polyomavirus 6 (OR, 0.44; 95% CI, 0.26-0.73) compared with their seronegative counterparts. Seropositivity to Epstein-Barr virus was negatively associated with eczema at age 4 years (OR, 0.39; 95% CI, 0.22-0.67) and 6 years (OR, 0.50; 95% CI, 0.25-0.99). Children with a higher burden of herpesviruses or of skin polyomaviruses had the lowest odds of eczema at age 4 years. Higher odds for asthma at age 4 years were found for WUPyV-seropositive children (OR, 3.98; 95% CI, 1.38-11.51), and for children seropositive to both respiratory polyomaviruses (KIPyV and WUPyV) (OR, 7.35; 95% CI, 1.66-32.59) compared with children seronegative to both. No associations were observed for rhinoconjunctivitis. There was no evidence of mediation by immune biomarkers. A heterogeneous pattern of infections and allergic diseases was observed with common infections associated with a decreased eczema risk and an increased asthma risk in children.

Sections du résumé

BACKGROUND
Evidence suggests a complex interplay between infections and allergic diseases.
OBJECTIVE
To explore the association of 14 common viruses with eczema, asthma, and rhinoconjunctivitis in childhood.
METHODS
We used cross-sectional (n = 686) and prospective (n = 440) data from children participating in the Rhea birth cohort. Immunoglobulin G to polyomaviruses (BK polyomavirus, JC polyomavirus, KI polyomavirus [KIPyV], WU polyomavirus [WUPyV], human polyomavirus 6, human polyomavirus 7, Trichodysplasia spinulosa polyomavirus, Merkel cell polyomavirus, human polyomavirus 9, and human polyomavirus 10) and herpesviruses (Epstein-Barr virus, Cytomegalovirus, Herpes simplex virus-1, Herpes simplex virus-2) were measured at age 4 years by fluorescent bead-based multiplex serology. Definitions of eczema, asthma, and rhinoconjunctivitis at ages 4 and 6 years were based on questionnaires. Mediation of the associations by immune biomarkers was tested.
RESULTS
Less likely to have eczema at age 4 years were KIPyV-seropositive (odds ratio [OR], 0.47; 95% confidence interval [CI], 0.27-0.82) and human polyomavirus 6 (OR, 0.44; 95% CI, 0.26-0.73) compared with their seronegative counterparts. Seropositivity to Epstein-Barr virus was negatively associated with eczema at age 4 years (OR, 0.39; 95% CI, 0.22-0.67) and 6 years (OR, 0.50; 95% CI, 0.25-0.99). Children with a higher burden of herpesviruses or of skin polyomaviruses had the lowest odds of eczema at age 4 years. Higher odds for asthma at age 4 years were found for WUPyV-seropositive children (OR, 3.98; 95% CI, 1.38-11.51), and for children seropositive to both respiratory polyomaviruses (KIPyV and WUPyV) (OR, 7.35; 95% CI, 1.66-32.59) compared with children seronegative to both. No associations were observed for rhinoconjunctivitis. There was no evidence of mediation by immune biomarkers.
CONCLUSION
A heterogeneous pattern of infections and allergic diseases was observed with common infections associated with a decreased eczema risk and an increased asthma risk in children.

Identifiants

pubmed: 33895421
pii: S1081-1206(21)00302-1
doi: 10.1016/j.anai.2021.04.019
pmc: PMC8801162
mid: NIHMS1759227
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

191-199.e3

Subventions

Organisme : NIEHS NIH HHS
ID : P30 ES007048
Pays : United States

Informations de copyright

Copyright © 2021 American College of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved.

Références

Clin Exp Allergy. 2009 Apr;39(4):509-17
pubmed: 19055650
J Allergy Clin Immunol. 2002 Nov;110(5):811-3
pubmed: 12417894
J Allergy Clin Immunol. 2019 Jan;143(1):26-35
pubmed: 30476499
Semin Immunopathol. 2020 Feb;42(1):61-74
pubmed: 31989228
J Allergy Clin Immunol. 2001 Apr;107(4):567-74
pubmed: 11295640
Epidemiology. 1990 Jan;1(1):43-6
pubmed: 2081237
J Allergy Clin Immunol. 2010 Feb;125(2):433-8
pubmed: 19963258
BMC Health Serv Res. 2017 Mar 14;17(1):201
pubmed: 28288628
Lancet Respir Med. 2014 Feb;2(2):131-40
pubmed: 24503268
Emerg Infect Dis. 2008 Nov;14(11):1766-8
pubmed: 18976566
Clin Exp Allergy. 2020 Apr;50(4):499-507
pubmed: 32037652
Curr Probl Dermatol. 2011;41:1-34
pubmed: 21576944
BMC Pulm Med. 2011 May 14;11:24
pubmed: 21569568
Emerg Infect Dis. 2012 Oct;18(10):1580-8
pubmed: 23017213
Front Cell Infect Microbiol. 2018 May 25;8:177
pubmed: 29888215
Front Pediatr. 2019 Mar 19;7:72
pubmed: 30941335
Psychol Methods. 2013 Jun;18(2):137-50
pubmed: 23379553
Allergy Asthma Proc. 2011 Nov-Dec;32(6):56-62
pubmed: 22221431
Stat Med. 2011 Feb 20;30(4):377-99
pubmed: 21225900
Med Microbiol Immunol. 2012 Feb;201(1):17-23
pubmed: 21614514
BMJ. 2000 Feb 12;320(7232):412-7
pubmed: 10669445
Emerg Infect Dis. 2008 Nov;14(11):1787-9
pubmed: 18976572
J Allergy Clin Immunol. 2007 Sep;120(3):673-9
pubmed: 17586034
Pediatr Allergy Immunol. 1997 May;8(2):91-6
pubmed: 9617779
Am J Epidemiol. 2016 Apr 1;183(7):671-9
pubmed: 26968942
Front Pediatr. 2018 Aug 17;6:228
pubmed: 30175090
J Allergy Clin Immunol. 2020 Sep;146(3):555-570
pubmed: 32320734
Br J Dermatol. 2020 Jun;182(6):1331-1342
pubmed: 31677162
Int Arch Allergy Appl Immunol. 1984;75(2):179-83
pubmed: 6088400
J Invest Dermatol. 2017 Dec;137(12):2460-2461
pubmed: 29169458
BMJ. 1997 Apr 5;314(7086):999-1003
pubmed: 9112843
Am J Epidemiol. 2010 Dec 15;172(12):1339-48
pubmed: 21036955
Health Sci Rep. 2018 Jul 18;1(8):e59
pubmed: 30623094
Br J Dermatol. 2005 Feb;152(2):202-16
pubmed: 15727630
Thorax. 2006 Jan;61(1):3-5
pubmed: 16396950
Vaccines (Basel). 2020 Apr 26;8(2):
pubmed: 32357557
J Allergy Clin Immunol. 2017 Jan;139(1):166-172
pubmed: 27609659
J Allergy Clin Immunol. 2015 Jul;136(1):81-86.e4
pubmed: 25910716
J Allergy Clin Immunol. 2017 Oct;140(4):909-920
pubmed: 28987220
J Allergy Clin Immunol. 2003 Apr;111(4):847-53
pubmed: 12704368
J Allergy Clin Immunol. 2015 Jul;136(1):3-13
pubmed: 26145982
Immunol Allergy Clin North Am. 2019 Aug;39(3):391-401
pubmed: 31284928
JCI Insight. 2018 May 3;3(9):
pubmed: 29720571
Pediatr Allergy Immunol. 2013 Feb;24(1):61-5
pubmed: 23331530
J Asthma Allergy. 2018 Aug 13;11:173-180
pubmed: 30147342
J Invest Dermatol. 2019 Feb;139(2):285-292
pubmed: 30470393
Thorax. 2000 Aug;55 Suppl 1:S2-10
pubmed: 10943631
Pediatr Allergy Immunol. 2011 Mar;22(2):243-8
pubmed: 20573034
Pediatr Allergy Immunol. 2019 Sep;30(6):604-613
pubmed: 31188509
BMJ Open. 2017 Apr 3;7(4):e013034
pubmed: 28373249
Immunol Allergy Clin North Am. 2019 Aug;39(3):xv-xvi
pubmed: 31284933
J Allergy Clin Immunol. 2012 Feb;129(2):359-67, 367.e1-3
pubmed: 22035877
Cytokine. 2019 May;117:1-7
pubmed: 30772773
Int Arch Allergy Appl Immunol. 1981;64(3):314-9
pubmed: 6260689
Allergy. 2019 Mar;74(3):518-526
pubmed: 30144084
Genome Biol. 2017 Jan 19;18(1):12
pubmed: 28103897
Int J Epidemiol. 2017 Oct 1;46(5):1392-1393k
pubmed: 29040580
Int J Epidemiol. 2004 Feb;33(1):199-207
pubmed: 15075169
Immunobiology. 2007;212(6):433-9
pubmed: 17544828

Auteurs

Marianna Karachaliou (M)

Barcelona Institute for Global Health (ISGlobal), Barcelona, Spain; Department of Social Medicine, Faculty of Medicine, University of Crete, Heraklion, Greece. Electronic address: marianna.karachaliou@isglobal.org.

Silvia de Sanjose (S)

National Cancer Institute (NCI), Rockville, Maryland.

Theano Roumeliotaki (T)

Department of Social Medicine, Faculty of Medicine, University of Crete, Heraklion, Greece.

Katerina Margetaki (K)

Department of Social Medicine, Faculty of Medicine, University of Crete, Heraklion, Greece.

Marina Vafeiadi (M)

Department of Social Medicine, Faculty of Medicine, University of Crete, Heraklion, Greece.

Tim Waterboer (T)

Infections and Cancer Division, Infection, Inflammation, and Cancer Research Program, German Cancer Research Center (DKFZ), Heidelberg, Germany.

Leda Chatzi (L)

Department of Preventive Medicine, Keck School of Medicine, University of Southern California, Los Angeles, California.

Manolis Kogevinas (M)

Barcelona Institute for Global Health (ISGlobal), Barcelona, Spain; Centro de Investigación Biomédica en Red de Epidemiología y Salud Pública (CIBERESP), Madrid, Spain; Hospital del Mar Medical Research Institute (IMIM), Barcelona, Spain; Universitat Pompeu Fabra (UPF), Barcelona, Spain.

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