van Dam, Koos P. J.
Volkers, Adriaan G.
Wieske, Luuk
Stalman, Eileen W.
Kummer, Laura Y. L.
van Kempen, Zoé L. E.
Killestein, Joep
Tas, Sander W.
Boekel, Laura
Wolbink, Gerrit J.
van der Kooi, Anneke J.
Raaphorst, Joost
Takkenberg, R. Bart
D’Haens, Geert R. A. M.
Spuls, Phyllis I.
Bekkenk, Marcel W.
Musters, Annelie H.
Post, Nicoline F.
Bosma, Angela L.
Hilhorst, Marc L.
Vegting, Yosta
Bemelman, Frederike J.
Voskuyl, Alexandre E.
Broens, Bo
Sanchez, Agner Parra
van Els, Cécile A. C. M.
de Wit, Jelle
Rutgers, Abraham
de Leeuw, Karina
Horváth, Barbara
Verschuuren, Jan J. G. M.
Ruiter, Annabel M.
van Ouwerkerk, Lotte
van der Woude, Diane
Allaart, Renée C. F.
Teng, Y. K. Onno
van Paassen, Pieter
Busch, Matthias H.
Jallah, Papay B. P.
Brusse, Esther
van Doorn, Pieter A.
Baars, Adája E.
Hijnen, Dirk Jan
Schreurs, Corine R. G.
van der Pol, W. Ludo
Goedee, H. Stephan
Steenhuis, Maurice
Keijzer, Sofie
Keijser, Jim B. D.
Cristianawati, Olvi
ten Brinke, Anja
Verstegen, Niels J. M.
van Ham, S. Marieke
Rispens, Theo
Kuijpers, Taco W.
Löwenberg, Mark
Eftimov, Filip https://orcid.org/0000-0002-2602-4364
,
Funding for this research was provided by:
ZonMw (10430072010007)
Article History
Received: 15 November 2022
Accepted: 29 April 2023
First Online: 17 May 2023
Declarations
:
: This study was approved by the medical ethical committee, and all participants provided signed informed consent (NL74974.018.20, EudraCT 2021–001102-30, Dutch Trial Register Trial ID: NL8900).
: Not applicable.
: Joep Killestein, has speaking relationships with Merck, Biogen, TEVA, Sanofi, Genzyme, Roche and Novartis. AmsterdamUMC, location VUmc, MS Center Amsterdam has received financial support for research activities from Merck, Celgene, Biogen, GlaxoSmithKline, Immunic, Roche, Teva, Sanofi, Genzyme, and Novartis. Geert D’Haens has been a consultant for AbbVie, Agomab, AstraZeneca, AM Pharma, AMT, Arena Pharmaceuticals, Bristol Meiers Squibb, Boehringer Ingelheim, Celltrion, Eli Lilly, Exeliom Biosciences, Exo Biologics, Galapagos, Index Pharmaceuticals, Kaleido, Roche, Gilead, GlaxoSmithKline, Gossamerbio, Pfizer, Immunic, Johnson & Johnson, Origo, Polpharma, Procise Diagnostics, Prometheus Laboratories, Prometheus Biosciences, Progenity, and Protagonist; and has received speaker’s bureau fees from AbbVie, Arena Pharmaceuticals, Galapagos, Gilead, Pfizer, BMS, and Takeda. Phyllis Spuls is involved in performing clinical trials with many pharmaceutical industries that manufacture drugs used for the treatment of e.g. psoriasis and atopic dermatitis, for which financial compensation is paid to the department/hospital and is one of the main investigator of the TREAT registry taskforce and SECURE-AD registry. Barbara Horváth reports fees from Janssen-Cilag (Advisory Boards, Educational grants, Consultations, Investigator Initiative Studies), AbbVie (Advisory Boards, Educational grants, Consultations, Investigator Initiative Studies), Novartis Pharma (Advisory Boards, Consultations, Investigator Initiative Studies), UCB Pharma (Advisory Boards, Consultations), Leo Pharma (Consultations), Solenne B.V. (Investigator Initiative Studies), Celgene (Consultations, Investigator Initiative Studies), Akari therapeutics (Consultations, Investigator Initiative Studies), Philips (Consultation), Roche (Consultation), Regeneron (Consultation) and Sanofi (Consultation), Argenx (Advisory Boards, Consultations) which fees were paid to the institution. Jan Verschuuren receives financial support from Target to B consortium, Prinses Beatrix Spierfonds, and has been involved in trials or consultancies for Argenx, Alexion, Rapharma. He is coinventor on patent applications based on MuSK-related research. The LUMC received royalties from IBL and Argenx for MG research. All reimbursements were received by the LUMC. The authors are members of the European Reference Network for Rare Neuromuscular Diseases [ERN EURO-NMD]. DirkJan Hijnen is investigator for AbbVie, LEO pharma, MedImmune/AstraZeneca, Novartis, Sanofi/Regeneron; consultancies for Regeneron/Sanofi, LEO pharma, MedImmune/AstraZeneca, Novartis, Incyte, Janssen, Pfizer. Mark Löwenberg has served as speaker and/or principal investigator for: Abbvie, Alimentiv, Bristol Myers Squibb, Celgene, Covidien, Dr. Falk, Ferring Pharmaceuticals, Galapagos, Gilead, GlaxoSmithKline, Janssen-Cilag, Merck Sharp & Dohme, Pfizer, Protagonist therapeutics, Receptos, Takeda, Tillotts, Tramedico. He has received research grants from AbbVie, Merck Sharp & Dohme, Dr Falk, Achmea healthcare, Galapagos and ZonMW. Filip Eftimov reports (governmental) grants from ZonMw (the Netherlands Organization for Health Research and Development) to study immune responses after SARS-CoV-2 vaccination in autoimmune diseases. He also received grants from Prinses Beatrix Spierfonds, CSL Behring, Kedrion, Terumo BCT, Grifols, Takeda Pharmaceutical Company, and Guillain-Barré Syndrome-Chronic Inflammatory Demyelinating Polyneuropathy (GBS-CIDP) Foundation; consulting fees from UCB Pharma and CSl Behring; and honoraria from Grifols. Diane van der Woude has received research grants from Inova diagnostics, FOREUM (Foundation for Research in Rheumatology) and ZonMw (the Netherlands Organization for Health Research and Development), as well as consulting fees from Galapagos. All other authors had no conflicts of interest. The authors/Several authors of this publication are members of the Netherlands Neuromuscular Center (NL-NMD) and the European Reference Network for rare neuromuscular diseases EURO-NMD.