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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

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 natu...

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Autores principales: Carrabba, Maria, Dellepiane, Rosa Maria, Cortesi, Manuela, Baselli, Lucia Augusta, Soresina, Annarosa, Cirillo, Emilia, Giardino, Giuliana, Conti, Francesca, Dotta, Laura, Finocchi, Andrea, Cancrini, Caterina, Milito, Cinzia, Pacillo, Lucia, Cinicola, Bianca Laura, Cossu, Fausto, Consolini, Rita, Montin, Davide, Quinti, Isabella, Pession, Andrea, Fabio, Giovanna, Pignata, Claudio, Pietrogrande, Maria Cristina, Badolato, Raffaele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10115605/
https://www.ncbi.nlm.nih.gov/pubmed/37081481
http://dx.doi.org/10.1186/s13223-023-00776-5
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author Carrabba, Maria
Dellepiane, Rosa Maria
Cortesi, Manuela
Baselli, Lucia Augusta
Soresina, Annarosa
Cirillo, Emilia
Giardino, Giuliana
Conti, Francesca
Dotta, Laura
Finocchi, Andrea
Cancrini, Caterina
Milito, Cinzia
Pacillo, Lucia
Cinicola, Bianca Laura
Cossu, Fausto
Consolini, Rita
Montin, Davide
Quinti, Isabella
Pession, Andrea
Fabio, Giovanna
Pignata, Claudio
Pietrogrande, Maria Cristina
Badolato, Raffaele
author_facet Carrabba, Maria
Dellepiane, Rosa Maria
Cortesi, Manuela
Baselli, Lucia Augusta
Soresina, Annarosa
Cirillo, Emilia
Giardino, Giuliana
Conti, Francesca
Dotta, Laura
Finocchi, Andrea
Cancrini, Caterina
Milito, Cinzia
Pacillo, Lucia
Cinicola, Bianca Laura
Cossu, Fausto
Consolini, Rita
Montin, Davide
Quinti, Isabella
Pession, Andrea
Fabio, Giovanna
Pignata, Claudio
Pietrogrande, Maria Cristina
Badolato, Raffaele
author_sort Carrabba, Maria
collection PubMed
description 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. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13223-023-00776-5.
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spelling pubmed-101156052023-04-21 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 Carrabba, Maria Dellepiane, Rosa Maria Cortesi, Manuela Baselli, Lucia Augusta Soresina, Annarosa Cirillo, Emilia Giardino, Giuliana Conti, Francesca Dotta, Laura Finocchi, Andrea Cancrini, Caterina Milito, Cinzia Pacillo, Lucia Cinicola, Bianca Laura Cossu, Fausto Consolini, Rita Montin, Davide Quinti, Isabella Pession, Andrea Fabio, Giovanna Pignata, Claudio Pietrogrande, Maria Cristina Badolato, Raffaele Allergy Asthma Clin Immunol Research 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. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13223-023-00776-5. BioMed Central 2023-04-20 /pmc/articles/PMC10115605/ /pubmed/37081481 http://dx.doi.org/10.1186/s13223-023-00776-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Carrabba, Maria
Dellepiane, Rosa Maria
Cortesi, Manuela
Baselli, Lucia Augusta
Soresina, Annarosa
Cirillo, Emilia
Giardino, Giuliana
Conti, Francesca
Dotta, Laura
Finocchi, Andrea
Cancrini, Caterina
Milito, Cinzia
Pacillo, Lucia
Cinicola, Bianca Laura
Cossu, Fausto
Consolini, Rita
Montin, Davide
Quinti, Isabella
Pession, Andrea
Fabio, Giovanna
Pignata, Claudio
Pietrogrande, Maria Cristina
Badolato, Raffaele
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
title 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
title_full 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
title_fullStr 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
title_full_unstemmed 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
title_short 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
title_sort 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
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10115605/
https://www.ncbi.nlm.nih.gov/pubmed/37081481
http://dx.doi.org/10.1186/s13223-023-00776-5
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