The Inborn Errors of Immunity—Virtual Consultation System Platform in Service for the Italian Primary Immunodeficiency Network: Results from the Validation Phase
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Published:2024-01-17
Issue:2
Volume:44
Page:
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ISSN:0271-9142
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Container-title:Journal of Clinical Immunology
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language:en
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Short-container-title:J Clin Immunol
Author:
Coppola Emma, Sgrulletti Mayla, Cortesi Manuela, Romano Roberta, Cirillo Emilia, Giardino Giuliana, Dotta Laura, Cancrini Caterina, Bruzzese Dario, Badolato Raffaele, Moschese Viviana, Pignata ClaudioORCID, , Alessandro Aiuti, Amodio Donato, Azzari Chiara, Canessa Clementina, Caorsi Roberta, Castagnoli Riccardo, Cicalese Maria Pia, Conti Francesca, Consolini Rita, Dellepiane Rosa Maria, Finocchi Andrea, Gallo Vera, Gattorno Marco, Graziani Simona, Lippi Francesca, Lougaris Vassilios, Martire Baldassarre, Matucci Andrea, Marzollo Antonio, Milito Cinzia, Montin Davide, Ottaviano Giorgio, Palma Paolo, Patuzzo Giuseppe, Pession Andrea, Pietrogrande Maria Cristina, Plebani Alessandro, Quinti Isabella, Ricci Silvia, Saettini Francesco, Soresina Annarosa, Spadaro Giuseppe, Tommasini Alberto, Trizzino Nino, Volpi Stefano, Vultaggio Alessandra, Zunica Fiammetta
Abstract
Abstract
Purpose
Inborn errors of immunity (IEI) represent a heterogeneous group of rare genetically determined diseases. In some cases, patients present with complex or atypical phenotypes, not fulfilling the accepted diagnostic criteria for IEI and, thus, at high risk of misdiagnosis or diagnostic delay. This study aimed to validate a platform that, through the opinion of immunologist experts, improves the diagnostic process and the level of care of patients with atypical/complex IEI.
Methods
Here, we describe the functioning of the IEI-Virtual Consultation System (VCS), an innovative platform created by the Italian Immunodeficiency Network (IPINet).
Results
In the validation phase, from January 2020 to June 2021, 68 cases were entered on the IEI-VCS platform. A final diagnosis was achieved in 35/68 cases (51%, 95% CI 38.7 to 64.2). In 22 out of 35 solved cases, the diagnosis was confirmed by genetic analysis. In 3/35 cases, a diagnosis of secondary immunodeficiency was made. In the remaining 10 cases, an unequivocal clinical and immunological diagnosis was obtained, even though not substantiated by genetic analysis.
Conclusion
From our preliminary study, the VCS represents an innovative and useful system to improve the diagnostic process of patients with complex unsolved IEI disorders, with benefits both in terms of reduction of time of diagnosis and access to the required therapies. These results may help the functioning of other international platforms for the management of complex cases.
Funder
European Union Bando Ricerca Finalizzata Ministero della Salute 2019 Università degli Studi di Napoli Federico II
Publisher
Springer Science and Business Media LLC
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