Long term longitudinal follow-up of an AD-HIES cohort: the impact of early diagnosis and enrollment to IPINet centers on the natural history of Job's syndrome.

AD-HIES COVID-19 Immunodeficiency Inborn errors of immunity Job’s syndrome Mucocutaneous candidiasis Pneumatocele STAT3 Staphylococcal infections

Journal

Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology
ISSN: 1710-1484
Titre abrégé: Allergy Asthma Clin Immunol
Pays: England
ID NLM: 101244313

Informations de publication

Date de publication:
20 Apr 2023
Historique:
received: 30 06 2022
accepted: 20 02 2023
medline: 21 4 2023
pubmed: 21 4 2023
entrez: 20 04 2023
Statut: epublish

Résumé

Job's syndrome, or autosomal dominant hyperimmunoglobulin E syndrome (AD-HIES, STAT3-Dominant Negative), is a rare inborn error of immunity (IEI) with multi-organ involvement and long-life post-infective damage. Longitudinal registries are of primary importance in improving our knowledge of the natural history and management of these rare disorders. This study aimed to describe the natural history of 30 Italian patients with AD-HIES recorded in the Italian network for primary immunodeficiency (IPINet) registry. This study shows the incidence of manifestations present at the time of diagnosis versus those that arose during follow up at a referral center for IEI. The mean time of diagnostic delay was 13.7 years, while the age of disease onset was < 12 months in 66.7% of patients. Respiratory complications, namely bronchiectasis and pneumatoceles, were present at diagnosis in 46.7% and 43.3% of patients, respectively. Antimicrobial prophylaxis resulted in a decrease in the incidence of pneumonia from 76.7% to 46.7%. At the time of diagnosis, skin involvement was present in 93.3% of the patients, including eczema (80.8%) and abscesses (66.7%). At the time of follow-up, under therapy, the prevalence of complications decreased: eczema and skin abscesses reduced to 63.3% and 56.7%, respectively. Antifungal prophylaxis decreased the incidence of mucocutaneous candidiasis from 70% to 56.7%. During the SARS-CoV-2 pandemic, seven patients developed COVID-19. Survival analyses showed that 27 out of 30 patients survived, while three patients died at ages of 28, 39, and 46 years as a consequence of lung bleeding, lymphoma, and sepsis, respectively. Analysis of a cumulative follow-up period of 278.7 patient-years showed that early diagnosis, adequate management at expertise centers for IEI, prophylactic antibiotics, and antifungal therapy improve outcomes and can positively influence the life expectancy of patients.

Identifiants

pubmed: 37081481
doi: 10.1186/s13223-023-00776-5
pii: 10.1186/s13223-023-00776-5
pmc: PMC10115605
doi:

Types de publication

Journal Article

Langues

eng

Pagination

32

Subventions

Organisme : Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico
ID : RC 2022

Informations de copyright

© 2023. The Author(s).

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Auteurs

Maria Carrabba (M)

Department of Internal Medicine, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy. maria.carrabba@gmail.com.

Rosa Maria Dellepiane (RM)

Department of Pediatrics, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.

Manuela Cortesi (M)

Pediatrics Clinic and Institute for Molecular Medicine A. Nocivelli, Department of Clinical and Experimental Sciences, University of Brescia and ASST-Spedali Civili di Brescia, Brescia, Italy.

Lucia Augusta Baselli (LA)

Department of Pediatrics, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.

Annarosa Soresina (A)

Pediatrics Clinic and Institute for Molecular Medicine A. Nocivelli, Department of Clinical and Experimental Sciences, University of Brescia and ASST-Spedali Civili di Brescia, Brescia, Italy.

Emilia Cirillo (E)

Pediatric Section, Department of Translational Medical Science, Federico II University, Naples, Italy.

Giuliana Giardino (G)

Pediatric Section, Department of Translational Medical Science, Federico II University, Naples, Italy.

Francesca Conti (F)

Pediatric Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.

Laura Dotta (L)

Pediatrics Clinic and Institute for Molecular Medicine A. Nocivelli, Department of Clinical and Experimental Sciences, University of Brescia and ASST-Spedali Civili di Brescia, Brescia, Italy.

Andrea Finocchi (A)

Academic Department of Pediatrics (DPUO), Immune and Infectious Diseases Division, Research Unit of Primary Immunodeficiencies, IRCCS, Bambino Gesù Children's Hospital, Rome, Italy.
Chair of Pediatrics, Department of Systems Medicine, University of Rome ''Tor Vergata'', Rome, Italy.

Caterina Cancrini (C)

Academic Department of Pediatrics (DPUO), Immune and Infectious Diseases Division, Research Unit of Primary Immunodeficiencies, IRCCS, Bambino Gesù Children's Hospital, Rome, Italy.
Chair of Pediatrics, Department of Systems Medicine, University of Rome ''Tor Vergata'', Rome, Italy.

Cinzia Milito (C)

Department of Molecular Medicine, "Sapienza" University of Roma, Rome, Italy.

Lucia Pacillo (L)

Academic Department of Pediatrics (DPUO), Immune and Infectious Diseases Division, Research Unit of Primary Immunodeficiencies, IRCCS, Bambino Gesù Children's Hospital, Rome, Italy.
Chair of Pediatrics, Department of Systems Medicine, University of Rome ''Tor Vergata'', Rome, Italy.

Bianca Laura Cinicola (BL)

Department of Molecular Medicine, "Sapienza" University of Roma, Rome, Italy.
Department of Maternal Infantile and Urological Sciences, "Sapienza" University of Rome, Rome, Italy.

Fausto Cossu (F)

Pediatric Clinic, Antonio Cao Hospital, Cagliari, Italy.

Rita Consolini (R)

Section of Pediatrics Immunology and Rheumatology, Department of Pediatrics, University of Pisa, Pisa, Italy.

Davide Montin (D)

Division of Pediatric Immunology and Rheumatology, Department of Public Health and Pediatrics, "Regina Margherita" Children Hospital, University of Turin, Turin, Italy.

Isabella Quinti (I)

Department of Molecular Medicine, "Sapienza" University of Roma, Rome, Italy.

Andrea Pession (A)

Pediatric Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.

Giovanna Fabio (G)

Department of Internal Medicine, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.

Claudio Pignata (C)

Pediatric Section, Department of Translational Medical Science, Federico II University, Naples, Italy.

Maria Cristina Pietrogrande (MC)

Department of Pediatrics, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Università Degli Studi of Milan, Milan, Italy.

Raffaele Badolato (R)

Pediatrics Clinic and Institute for Molecular Medicine A. Nocivelli, Department of Clinical and Experimental Sciences, University of Brescia and ASST-Spedali Civili di Brescia, Brescia, Italy.

Classifications MeSH