Inborn Errors of Immunity Associated With Type 2 Inflammation in the USIDNET Registry.

IgE atopy eosinophilia inborn error of immunity primary immunodeficiency

Journal

Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960

Informations de publication

Date de publication:
2022
Historique:
received: 08 12 2021
accepted: 27 01 2022
entrez: 11 3 2022
pubmed: 12 3 2022
medline: 3 5 2022
Statut: epublish

Résumé

Monogenic conditions that disrupt proper development and/or function of the immune system are termed inborn errors of immunity (IEIs), also known as primary immunodeficiencies. Patients with IEIs often suffer from other manifestations in addition to infection, and allergic inflammation is an increasingly recognized feature of these conditions. We performed a retrospective analysis of IEIs presenting with allergic inflammation as reported in the USIDNET registry. Our inclusion criteria comprised of patients with a reported monogenic cause for IEI where reported lab eosinophil and/or IgE values were available for the patient prior to them receiving potentially curative therapy. Patients were excluded if we were unable to determine the defective gene underlying their IEI. Patients were classified as having eosinophilia or elevated IgE when their record included at least 1 eosinophil count or IgE value that was greater than the age stratified upper limit of normal. We compared the proportion of patients with eosinophilia or elevated IgE with the proportion of samples in a reference population that fall above the upper limit of normal (2.5%). The query submitted to the USIDNET registry identified 1409 patients meeting inclusion criteria with a monogenic cause for their IEI diagnosis, of which 975 had eosinophil counts and 645 had IgE levels obtained prior to transplantation or gene therapy that were available for analysis. Overall, 18.8% (183/975) of the patients evaluated from the USIDNET registry had eosinophilia and 20.9% (135/645) had an elevated IgE. IEIs caused by defects in 32 genes were found to be significantly associated with eosinophilia and/or an elevated IgE level, spanning 7 of the 10 IEI categories according to the International Union of Immunological Societies classification. Type 2 inflammation manifesting as eosinophilia or elevated IgE is found in a broad range of IEIs in the USIDNET registry. Our findings suggest that allergic immune dysregulation may be more widespread in IEIs than previously reported.

Sections du résumé

Background
Monogenic conditions that disrupt proper development and/or function of the immune system are termed inborn errors of immunity (IEIs), also known as primary immunodeficiencies. Patients with IEIs often suffer from other manifestations in addition to infection, and allergic inflammation is an increasingly recognized feature of these conditions.
Methods
We performed a retrospective analysis of IEIs presenting with allergic inflammation as reported in the USIDNET registry. Our inclusion criteria comprised of patients with a reported monogenic cause for IEI where reported lab eosinophil and/or IgE values were available for the patient prior to them receiving potentially curative therapy. Patients were excluded if we were unable to determine the defective gene underlying their IEI. Patients were classified as having eosinophilia or elevated IgE when their record included at least 1 eosinophil count or IgE value that was greater than the age stratified upper limit of normal. We compared the proportion of patients with eosinophilia or elevated IgE with the proportion of samples in a reference population that fall above the upper limit of normal (2.5%).
Results
The query submitted to the USIDNET registry identified 1409 patients meeting inclusion criteria with a monogenic cause for their IEI diagnosis, of which 975 had eosinophil counts and 645 had IgE levels obtained prior to transplantation or gene therapy that were available for analysis. Overall, 18.8% (183/975) of the patients evaluated from the USIDNET registry had eosinophilia and 20.9% (135/645) had an elevated IgE. IEIs caused by defects in 32 genes were found to be significantly associated with eosinophilia and/or an elevated IgE level, spanning 7 of the 10 IEI categories according to the International Union of Immunological Societies classification.
Conclusion
Type 2 inflammation manifesting as eosinophilia or elevated IgE is found in a broad range of IEIs in the USIDNET registry. Our findings suggest that allergic immune dysregulation may be more widespread in IEIs than previously reported.

Identifiants

pubmed: 35273610
doi: 10.3389/fimmu.2022.831279
pmc: PMC8902297
doi:

Substances chimiques

Immunoglobulin E 37341-29-0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

831279

Subventions

Organisme : CIHR
ID : PJQ-173584
Pays : Canada

Informations de copyright

Copyright © 2022 Smith, Dai, Modi, Sara, Garabedian, Marsh, Puck, Secord, Sullivan, Turvey, Biggs and the USIDNET Consortium.

Déclaration de conflit d'intérêts

JP receives royalties from UpToDate and her spouse is employed by and owns stock in Invitae, a gene sequencing company. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Références

Curr Opin Pediatr. 2018 Dec;30(6):848-854
pubmed: 30407976
Allergy Asthma Clin Immunol. 2016 May 24;12:27
pubmed: 27222657
Front Immunol. 2014 Dec 15;5:627
pubmed: 25566243
Cell Mol Life Sci. 2004 Sep;61(18):2361-85
pubmed: 15378206
J Pediatr Hematol Oncol. 2020 Oct;42(7):e601-e605
pubmed: 32049770
Front Immunol. 2018 Dec 12;9:2912
pubmed: 30619276
J Allergy Clin Immunol. 2017 Jul;140(1):273-277.e10
pubmed: 27965109
Curr Pediatr Rev. 2019;15(4):245-250
pubmed: 31530267
Immunol Allergy Clin North Am. 2015 Aug;35(3):523-44
pubmed: 26209898
J Clin Immunol. 2016 May;36 Suppl 1:57-67
pubmed: 27210535
Hematology Am Soc Hematol Educ Program. 2019 Dec 6;2019(1):457-465
pubmed: 31808905
Hum Mutat. 2017 Oct;38(10):1286-1296
pubmed: 28744922
Clin Immunol. 2017 Aug;181:75-82
pubmed: 28625885
Asthma Res Pract. 2015 Oct 20;1:10
pubmed: 27965764
J Allergy Clin Immunol. 2002 Nov;110(5):743-51
pubmed: 12417883
J Allergy Clin Immunol. 2021 Nov;148(5):1130-1139
pubmed: 34428518
Curr Opin Pulm Med. 2011 May;17(3):172-9
pubmed: 21415752
Can Respir J. 2010 Jan-Feb;17(1):e1-6
pubmed: 20186360
J Allergy Clin Immunol. 2022 Feb;149(2):736-746
pubmed: 34111452
Clin Exp Immunol. 2005 Jun;140(3):520-3
pubmed: 15932514
J Clin Immunol. 2020 Jan;40(1):24-64
pubmed: 31953710
Postgrad Med J. 2009 Dec;85(1010):660-6
pubmed: 20075404
J Allergy Clin Immunol. 2010 Feb;125(2 Suppl 2):S182-94
pubmed: 20042228
J Clin Immunol. 2018 Jan;38(1):13-27
pubmed: 29086100
J Allergy Clin Immunol Pract. 2020 Sep;8(8):2747-2760.e7
pubmed: 32428713
J Exp Med. 2018 Apr 2;215(4):1009-1022
pubmed: 29549114
J Allergy Clin Immunol. 2015 Sep;136(3):802-6
pubmed: 25865352
Immunity. 2015 May 19;42(5):890-902
pubmed: 25979420
Front Immunol. 2018 Jun 25;9:1439
pubmed: 29997619
Allergy. 2005 Nov;60(11):1357-60
pubmed: 16197466
Allergy. 2018 Nov;73(11):2122-2136
pubmed: 30043993
Front Immunol. 2020 Nov 05;11:582376
pubmed: 33224144
Allergy Asthma Clin Immunol. 2018 Sep 12;14(Suppl 2):61
pubmed: 30275850
Blood. 2012 Feb 16;119(7):1650-7
pubmed: 22180439
J Allergy Clin Immunol. 2015 Dec;136(6):1591-1600
pubmed: 26343451
Curr Opin Allergy Clin Immunol. 2019 Dec;19(6):571-577
pubmed: 31464718
Cell. 2016 Nov 17;167(5):1415-1429.e19
pubmed: 27863252
Nat Genet. 2017 Jul 27;49(8):1162-1163
pubmed: 28747751
Clin Mol Allergy. 2012 Jan 04;10(1):2
pubmed: 22216879
Annu Rev Immunol. 2020 Apr 26;38:785-808
pubmed: 32126183
J Clin Immunol. 2017 Feb;37(2):101-103
pubmed: 27966181
Pediatr Allergy Immunol. 2021 Nov;32(8):1796-1803
pubmed: 34097760
Autoimmun Rev. 2020 Jun;19(6):102526
pubmed: 32234571
J Allergy Clin Immunol. 2014 Feb;133(2):589-91
pubmed: 24139495
Immunol Res. 2018 Jun;66(3):367-380
pubmed: 29744770
Indian J Med Res. 2011 Aug;134:149-61
pubmed: 21911966
Cell. 2020 Sep 3;182(5):1198-1213.e14
pubmed: 32888493
Adv Ther. 2017 Dec;34(12):2543-2557
pubmed: 29168144
Front Immunol. 2021 Aug 03;12:718779
pubmed: 34413860
J Allergy Clin Immunol. 2009 Oct;124(4):779-85.e6
pubmed: 19767079
J Clin Immunol. 2020 Jul;40(5):671-681
pubmed: 32451662
Int J Mol Med. 2003 Aug;12(2):185-91
pubmed: 12851715
Cytokine X. 2020 Sep;2(3):100032
pubmed: 33015616
Inflammation. 2016 Dec;39(6):2045-2052
pubmed: 27614764
Indian J Pediatr. 2016 Apr;83(4):331-7
pubmed: 26909497
Pediatr Allergy Immunol. 2008 Mar;19(2):125-31
pubmed: 18086231
J Exp Med. 2021 Aug 2;218(8):
pubmed: 34160550
Am J Clin Pathol. 2020 Aug 5;154(3):330-341
pubmed: 32561916

Auteurs

Kelsey L Smith (KL)

Department of Pediatrics, University of British Columbia, Vancouver, BC, Canada.
British Columbia (BC) Children's Hospital, Vancouver, BC, Canada.

Darlene Dai (D)

Department of Pediatrics, University of British Columbia, Vancouver, BC, Canada.
British Columbia (BC) Children's Hospital, Vancouver, BC, Canada.

Bhavi P Modi (BP)

Department of Pediatrics, University of British Columbia, Vancouver, BC, Canada.
British Columbia (BC) Children's Hospital, Vancouver, BC, Canada.

Rahnuma Sara (R)

Department of Pediatrics, University of British Columbia, Vancouver, BC, Canada.
British Columbia (BC) Children's Hospital, Vancouver, BC, Canada.

Elizabeth Garabedian (E)

National Human Genome Research Institute, Bethesda, MD, United States.
National Institutes of Health, Bethesda, MD, United States.

Rebecca A Marsh (RA)

Cincinnati Children's Hospital, University of Cincinnati, Cincinnati, OH, United States.

Jennifer Puck (J)

Division of Allergy/Immunology and Blood and Marrow Transplantation, Department of Pediatrics, University of California, San Francisco, San Francisco, CA, United States.

Elizabeth Secord (E)

Wayne State University, Detroit, MI, United States.

Kathleen E Sullivan (KE)

Children's Hospital of Philadelphia, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, United States.

Stuart E Turvey (SE)

Department of Pediatrics, University of British Columbia, Vancouver, BC, Canada.
British Columbia (BC) Children's Hospital, Vancouver, BC, Canada.

Catherine M Biggs (CM)

Department of Pediatrics, University of British Columbia, Vancouver, BC, Canada.
British Columbia (BC) Children's Hospital, Vancouver, BC, Canada.
St Paul's Hospital, Vancouver, BC, Canada.

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