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Allogeneic hematopoietic stem cell transplantation for neuromyelitis optica

Authors :
Greco R
Vago L
Moiola L
Rossi P
Furlan R
Radaelli M
Martinelli V
Carbone MR
Lupo Stanghellini MT
Assanelli A
Bernardi M
Corti C
Peccatori J
Vezzulli P
BONDANZA , ATTILIO
MARTINO , GIANVITO
BONINI , MARIA CHIARA
FALINI , ANDREA
CICERI , FABIO
COMI , GIANCARLO
Greco, R
Bondanza, Attilio
Vago, L
Moiola, L
Rossi, P
Furlan, R
Martino, Gianvito
Radaelli, M
Martinelli, V
Carbone, Mr
Lupo Stanghellini, Mt
Assanelli, A
Bernardi, M
Corti, C
Peccatori, J
Bonini, MARIA CHIARA
Vezzulli, P
Falini, Andrea
Ciceri, Fabio
Comi, Giancarlo
Source :
Annals of neurology. 75(3)
Publication Year :
2013

Abstract

Neuromyelitis optica is a rare neurological autoimmune disorder characterized by a poor prognosis. Immunosuppression can halt disease progression, but some patients are refractory to multiple treatments, experiencing frequent relapses with accumulating disability. Here we report on durable clinical remissions after allogeneic hematopoietic stem cell transplantation in 2 patients suffering from severe forms of the disease. Immunological data evidenced disappearance of the pathogenic antibodies and regeneration of a naive immune system of donor origin. These findings correlated with evident clinical and radiological improvement in both patients, warranting extended clinical trials to investigate this promising therapeutic option. ANN NEUROL 2014;75:447-453 Neuromyelitis optica is a rare neurological autoimmune disorder characterized by a poor prognosis. Immunosuppression can halt disease progression, but some patients are refractory to multiple treatments, experiencing frequent relapses with accumulating disability. Here we report on durable clinical remissions after allogeneic hematopoietic stem cell transplantation in 2 patients suffering from severe forms of the disease. Immunological data evidenced disappearance of the pathogenic antibodies and regeneration of a naive immune system of donor origin. These findings correlated with evident clinical and radiological improvement in both patients, warranting extended clinical trials to investigate this promising therapeutic option.

Details

ISSN :
15318249
Volume :
75
Issue :
3
Database :
OpenAIRE
Journal :
Annals of neurology
Accession number :
edsair.pmid.dedup....1b131df707010c348865eaafc88bb419