Doneddu, Pietro Emiliano
Moretti, Giulia
Di Stefano, Vincenzo
Falzone, Yuri
Leonardi, Luca
Luigetti, Marco
Mataluni, Giorgia
Gentile, Luca
Carpo, Marinella
Barilaro, Alessandro
Filosto, Massimiliano
Vegezzi, Elisa
Inghilleri, Maurizio
Canale, Fabrizio
Brighina, Filippo
Matà, Sabrina
Ratti, Adele
Forcina, Francesca
Siconolfi, Giovanni
Lozi, Claudia
Mazzeo, Anna
Mollo, Ugo
Risi, Barbara
Cosentino, Giuseppe
Moret, Federica
Fasano, Carla
Todisco, Vincenzo
Russo, Massimo
Nobile–Orazio, Eduardo https://orcid.org/0000-0003-2624-8138
Funding for this research was provided by:
Alnylam Pharmaceuticals, Italy
Regione Lombardia
Ministero della Salute (Ricerca Finalizzata (Progetto RF-2016-02361887))
Kedrion Biopharma
CSL Behring
Humanitas Research Hospital
GBS/CIDP Foundation International
Article History
Received: 12 April 2025
Revised: 15 June 2025
Accepted: 17 June 2025
First Online: 16 July 2025
Declarations
:
: Pietro Emiliano Doneddu reports personal fees for Advisory from ArgenX, and received travel grants to attend scientific meetings from CSL Behring, and Kedrion. Giuseppe Cosentino has received travel grants to attend scientific meetings from CSL Behring, and Kedrion. Massimiliano Filosto has served on scientific advisory boards for CSL Behring, Sanofi, and Amicus, and has received travel grants from Sanofi, Biogen, Kedrion, and CSL Behring to attend scientific meeting. Anna Mazzeo has received travel grants from Kedrion, and CSL Behring to attend scientific meeting. Maurizio Inghilleri has received travel grants to attend scientific meetings from CSL Behring, ArgenX, and Alexion. Federica Moret has received travel grants to attend scientific meetings from CSL Behring, ArgenX, and Alexion. Eduardo Nobile-Orazio reports personal fees for Advisory or Scientific Board from ArgenX – Belgium, Takeda – Italy and USA, CSL-Behring—Italy and USA, Janssen – USA, Kedrion – Italy, LFB – France, Roche– Switzerland, Sanofi—USA. The authors declare that they have no conflict of interest.
: All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards. The study was approved by the Ethics Committee of each participating center and was conducted in accordance with the principles of the Declaration of Helsinki.
: Informed consent was obtained from all individual participants included in the study.