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Immune ablation and stem-cell therapy in autoimmune disease: Clinical experience

In the past 5 years, around 350 patients have received haematopoietic stem cell (HSC) transplantation for an autoimmune disease, with 275 of these registered in an international data base in Basel under the auspices of the European League Against Rheumatism (EULAR) and the European Group for Blood a...

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Detalles Bibliográficos
Autores principales: Tyndall, Alan, Gratwohl, Alois
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2000
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC130009/
https://www.ncbi.nlm.nih.gov/pubmed/11094441
http://dx.doi.org/10.1186/ar102
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author Tyndall, Alan
Gratwohl, Alois
author_facet Tyndall, Alan
Gratwohl, Alois
author_sort Tyndall, Alan
collection PubMed
description In the past 5 years, around 350 patients have received haematopoietic stem cell (HSC) transplantation for an autoimmune disease, with 275 of these registered in an international data base in Basel under the auspices of the European League Against Rheumatism (EULAR) and the European Group for Blood and Marrow Transplantation(EBMT). Most patients had either a progressive form of multiple sclerosis (MS; n = 88) or scleroderma (now called systemic sclerosis; n = 55). Other diseases were rheumatoid arthritis (Ra n = 40), juvenile idiopathic arthritis (JIA; n = 30), systemic lupus erythematosus (SLE; n = 20), idiopathic thrombocytopenic purpura (ITP; n = 7) and others. The procedure-related mortality was around 9%, with between-disease differences, being higher in systemic sclerosis and JIA and lower in RA (one death only). Benefit has been seen in around two-thirds of cases. No one regimen was clearly superior to another, with a trend toward more infectious complications with more intense regimens. Prospective, controlled randomized trials are indicated and being planned.
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spelling pubmed-1300092002-10-28 Immune ablation and stem-cell therapy in autoimmune disease: Clinical experience Tyndall, Alan Gratwohl, Alois Arthritis Res Review In the past 5 years, around 350 patients have received haematopoietic stem cell (HSC) transplantation for an autoimmune disease, with 275 of these registered in an international data base in Basel under the auspices of the European League Against Rheumatism (EULAR) and the European Group for Blood and Marrow Transplantation(EBMT). Most patients had either a progressive form of multiple sclerosis (MS; n = 88) or scleroderma (now called systemic sclerosis; n = 55). Other diseases were rheumatoid arthritis (Ra n = 40), juvenile idiopathic arthritis (JIA; n = 30), systemic lupus erythematosus (SLE; n = 20), idiopathic thrombocytopenic purpura (ITP; n = 7) and others. The procedure-related mortality was around 9%, with between-disease differences, being higher in systemic sclerosis and JIA and lower in RA (one death only). Benefit has been seen in around two-thirds of cases. No one regimen was clearly superior to another, with a trend toward more infectious complications with more intense regimens. Prospective, controlled randomized trials are indicated and being planned. BioMed Central 2000 2000-05-26 /pmc/articles/PMC130009/ /pubmed/11094441 http://dx.doi.org/10.1186/ar102 Text en Copyright © 2000 Current Science Ltd
spellingShingle Review
Tyndall, Alan
Gratwohl, Alois
Immune ablation and stem-cell therapy in autoimmune disease: Clinical experience
title Immune ablation and stem-cell therapy in autoimmune disease: Clinical experience
title_full Immune ablation and stem-cell therapy in autoimmune disease: Clinical experience
title_fullStr Immune ablation and stem-cell therapy in autoimmune disease: Clinical experience
title_full_unstemmed Immune ablation and stem-cell therapy in autoimmune disease: Clinical experience
title_short Immune ablation and stem-cell therapy in autoimmune disease: Clinical experience
title_sort immune ablation and stem-cell therapy in autoimmune disease: clinical experience
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC130009/
https://www.ncbi.nlm.nih.gov/pubmed/11094441
http://dx.doi.org/10.1186/ar102
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