TY - JOUR
T1 - Autologous haematopoietic stem cell transplantation and other cellular therapy in multiple sclerosis and immune-mediated neurological diseases
T2 - updated guidelines and recommendations from the EBMT Autoimmune Diseases Working Party (ADWP) and the Joint Accreditation Committee of EBMT and ISCT (JACIE)
AU - for the European Society for Blood and Marrow Transplantation (EBMT) Autoimmune Diseases Working Party (ADWP) and the Joint Accreditation Committee of the International Society for Cellular Therapy (ISCT) and EBMT (JACIE)
AU - Sharrack, Basil
AU - Saccardi, Riccardo
AU - Alexander, Tobias
AU - Badoglio, Manuela
AU - Burman, Joachim
AU - Farge, Dominique
AU - Greco, Raffaella
AU - Jessop, Helen
AU - Kazmi, Majid
AU - Kirgizov, Kirill
AU - Labopin, Myriam
AU - Mancardi, Gianluigi
AU - Martin, Roland
AU - Moore, John
AU - Muraro, Paolo A.
AU - Rovira, Montserrat
AU - Sormani, Maria Pia
AU - Snowden, John A.
AU - Snowden, John
AU - Saccardi, Riccardo
AU - McGrath, Eoin
AU - Bambi, Franco
AU - Sanchez-Guijo, Fermín
AU - Worel, Nina
AU - Snowden, John
AU - Alexander, Tobias
AU - Badolglio, Manuela
AU - Abinun, Mario
AU - Arnold, Renate
AU - Brierley, Charlotte
AU - Burman, Joachim
AU - Castilla-Llorente, Cristina
AU - Cooper, Nichola
AU - Daikeler, Thomas
AU - del Papa, Nicoletta
AU - Farge, Dominique
AU - Finke, Jurgen
AU - Reax, R.
AU - Hagglund, Hans
AU - Henes, Joerg
AU - Hiepe, Falk
AU - Jessop, Helen
AU - Kiely, David
AU - Labopin, Myriam
AU - Kazmi, Majid
AU - Kirgizov, Kirill
AU - Mancardi, Gianluigi
AU - Marjanovic, Zora
AU - Martin, Roland
AU - Sossa, Claudia
N1 - Publisher Copyright:
© 2019, Springer Nature Limited.
PY - 2020/2/1
Y1 - 2020/2/1
N2 - These updated EBMT guidelines review the clinical evidence, registry activity and mechanisms of action of haematopoietic stem cell transplantation (HSCT) in multiple sclerosis (MS) and other immune-mediated neurological diseases and provide recommendations for patient selection, transplant technique, follow-up and future development. The major focus is on autologous HSCT (aHSCT), used in MS for over two decades and currently the fastest growing indication for this treatment in Europe, with increasing evidence to support its use in highly active relapsing remitting MS failing to respond to disease modifying therapies. aHSCT may have a potential role in the treatment of the progressive forms of MS with a significant inflammatory component and other immune-mediated neurological diseases, including chronic inflammatory demyelinating polyneuropathy, neuromyelitis optica, myasthenia gravis and stiff person syndrome. Allogeneic HSCT should only be considered where potential risks are justified. Compared with other immunomodulatory treatments, HSCT is associated with greater short-term risks and requires close interspeciality collaboration between transplant physicians and neurologists with a special interest in these neurological conditions before, during and after treatment in accredited HSCT centres. Other experimental cell therapies are developmental for these diseases and patients should only be treated on clinical trials.
AB - These updated EBMT guidelines review the clinical evidence, registry activity and mechanisms of action of haematopoietic stem cell transplantation (HSCT) in multiple sclerosis (MS) and other immune-mediated neurological diseases and provide recommendations for patient selection, transplant technique, follow-up and future development. The major focus is on autologous HSCT (aHSCT), used in MS for over two decades and currently the fastest growing indication for this treatment in Europe, with increasing evidence to support its use in highly active relapsing remitting MS failing to respond to disease modifying therapies. aHSCT may have a potential role in the treatment of the progressive forms of MS with a significant inflammatory component and other immune-mediated neurological diseases, including chronic inflammatory demyelinating polyneuropathy, neuromyelitis optica, myasthenia gravis and stiff person syndrome. Allogeneic HSCT should only be considered where potential risks are justified. Compared with other immunomodulatory treatments, HSCT is associated with greater short-term risks and requires close interspeciality collaboration between transplant physicians and neurologists with a special interest in these neurological conditions before, during and after treatment in accredited HSCT centres. Other experimental cell therapies are developmental for these diseases and patients should only be treated on clinical trials.
UR - http://www.scopus.com/inward/record.url?scp=85075734955&partnerID=8YFLogxK
U2 - 10.1038/s41409-019-0684-0
DO - 10.1038/s41409-019-0684-0
M3 - Artículo Científico
C2 - 31558790
AN - SCOPUS:85075734955
SN - 0268-3369
VL - 55
SP - 283
EP - 306
JO - Bone Marrow Transplantation
JF - Bone Marrow Transplantation
IS - 2
ER -