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Activated phosphoinositide 3-kinase δ syndrome: Update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunity.

Authors :
Maccari ME
Wolkewitz M
Schwab C
Lorenzini T
Leiding JW
Aladjdi N
Abolhassani H
Abou-Chahla W
Aiuti A
Azarnoush S
Baris S
Barlogis V
Barzaghi F
Baumann U
Bloomfield M
Bohynikova N
Bodet D
Boutboul D
Bucciol G
Buckland MS
Burns SO
Cancrini C
Cathébras P
Cavazzana M
Cheminant M
Chinello M
Ciznar P
Coulter TI
D'Aveni M
Ekwall O
Eric Z
Eren E
Fasth A
Frange P
Fournier B
Garcia-Prat M
Gardembas M
Geier C
Ghosh S
Goda V
Hammarström L
Hauck F
Heeg M
Heropolitanska-Pliszka E
Hilfanova A
Jolles S
Karakoc-Aydiner E
Kindle GR
Kiykim A
Klemann C
Koletsi P
Koltan S
Kondratenko I
Körholz J
Krüger R
Jeziorski E
Levy R
Le Guenno G
Lefevre G
Lougaris V
Marzollo A
Mahlaoui N
Malphettes M
Meinhardt A
Merlin E
Meyts I
Milota T
Moreira F
Moshous D
Mukhina A
Neth O
Neubert J
Neven B
Nieters A
Nove-Josserand R
Oksenhendler E
Ozen A
Olbrich P
Perlat A
Pac M
Schmid JP
Pacillo L
Parra-Martinez A
Paschenko O
Pellier I
Sefer AP
Plebani A
Plantaz D
Prader S
Raffray L
Ritterbusch H
Riviere JG
Rivalta B
Rusch S
Sakovich I
Savic S
Scheible R
Schleinitz N
Schuetz C
Schulz A
Sediva A
Semeraro M
Sharapova SO
Shcherbina A
Slatter MA
Sogkas G
Soler-Palacin P
Speckmann C
Stephan JL
Suarez F
Tommasini A
Trück J
Uhlmann A
van Aerde KJ
van Montfrans J
von Bernuth H
Warnatz K
Williams T
Worth AJJ
Ip W
Picard C
Catherinot E
Nademi Z
Grimbacher B
Forbes Satter LR
Kracker S
Chandra A
Condliffe AM
Ehl S
Source :
The Journal of allergy and clinical immunology [J Allergy Clin Immunol] 2023 Oct; Vol. 152 (4), pp. 984-996.e10. Date of Electronic Publication: 2023 Jun 28.
Publication Year :
2023

Abstract

Background: Activated phosphoinositide-3-kinase δ syndrome (APDS) is an inborn error of immunity (IEI) with infection susceptibility and immune dysregulation, clinically overlapping with other conditions. Management depends on disease evolution, but predictors of severe disease are lacking.<br />Objectives: This study sought to report the extended spectrum of disease manifestations in APDS1 versus APDS2; compare these to CTLA4 deficiency, NFKB1 deficiency, and STAT3 gain-of-function (GOF) disease; and identify predictors of severity in APDS.<br />Methods: Data was collected from the ESID (European Society for Immunodeficiencies)-APDS registry and was compared with published cohorts of the other IEIs.<br />Results: The analysis of 170 patients with APDS outlines high penetrance and early onset of APDS compared to the other IEIs. The large clinical heterogeneity even in individuals with the same PIK3CD variant E1021K illustrates how poorly the genotype predicts the disease phenotype and course. The high clinical overlap between APDS and the other investigated IEIs suggests relevant pathophysiological convergence of the affected pathways. Preferentially affected organ systems indicate specific pathophysiology: bronchiectasis is typical of APDS1; interstitial lung disease and enteropathy are more common in STAT3 GOF and CTLA4 deficiency. Endocrinopathies are most frequent in STAT3 GOF, but growth impairment is also common, particularly in APDS2. Early clinical presentation is a risk factor for severe disease in APDS.<br />Conclusions: APDS illustrates how a single genetic variant can result in a diverse autoimmune-lymphoproliferative phenotype. Overlap with other IEIs is substantial. Some specific features distinguish APDS1 from APDS2. Early onset is a risk factor for severe disease course calling for specific treatment studies in younger patients.<br /> (Copyright © 2023 American Academy of Allergy, Asthma & Immunology. All rights reserved.)

Details

Language :
English
ISSN :
1097-6825
Volume :
152
Issue :
4
Database :
MEDLINE
Journal :
The Journal of allergy and clinical immunology
Publication Type :
Academic Journal
Accession number :
37390899
Full Text :
https://doi.org/10.1016/j.jaci.2023.06.015