MRI and CFS oligoclonal bands after autologus hematopoietic stem cell transplantation in MS

dc.contributor.authorSaiz Hinarejos, Albert
dc.contributor.authorCarreras Margalef, Esther
dc.contributor.authorBerenguer, Joan
dc.contributor.authorYagüe, Jordi
dc.contributor.authorMartínez, C.
dc.contributor.authorMarín, Pedro
dc.contributor.authorRovira, M.
dc.contributor.authorPujol Farré, Teresa
dc.contributor.authorArbizu Urdiain, Txomin
dc.contributor.authorGraus Ribas, Francesc
dc.date.accessioned2020-04-24T10:49:49Z
dc.date.available2020-04-24T10:49:49Z
dc.date.issued2001-04-24
dc.date.updated2020-04-24T10:49:49Z
dc.description.abstractTo analyze the MRI and CSF oligoclonal bands (OB) changes in patients with MS who underwent an autologous hematopoietic stem cell transplantation (AHSCT). Background: AHSCT is evaluated as an alternative therapy in severe MS. In previous series of AHSCT for MS, data on MRI or OB outcome were limited or not provided. Methods: five patients with a median Kurtzke's EDSS score of 6.5, more than two attacks, and confirmed worsening of the EDSS in the previous year received an AHSCT. Hematopoietic stem cells were mobilized with cyclophosphamide (3 g/m2) and granulocyte colony-stimulating factor (5 microg/kg/d). The graft was T cell depleted by positive CD 34+ selection. Conditioning regimen included BCNU (300 mg/m(2)), cyclophosphamide (150 mg/kg in 3 days), and antithymocyte globulin (60 mg/kg in 4 days). MRI scans were scheduled at baseline and 1, 3, 6, and 12 months and OB analysis at baseline and 3 and 12 months post-AHSCT. Results: four patients had a stable or improved EDSS after a median follow-up of 18 months (range, 12 to 24 months). The fifth patient's condition deteriorated during AHSCT. She partially improved and remained stable after month 3 after AHSCT. The baseline CSF OB persisted 1 year after AHSCT. MRI studies after AHSCT showed no enhanced T1 lesions and no new or enlarging T2 lesions. The median percentage change of T2 lesion load was -11.8% (range, -26.6 to -4.0%). All patients had a decrease of corpus callosum area at 1 year (median, 12.4%; range, 7.8% to 20.5%) that did not progress in the two patients evaluated at 2 years after AHSCT. Conclusions: although the persistence of CSF OB suggests the lymphocytes were not eliminated from the CNS, the follow-up MRI studies showed no enhanced T1 brain lesions and a reduction in the T2 lesion load that correlated with the clinical stabilization of MS after AHSCT.
dc.format.extent6 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec500862
dc.identifier.issn0028-3878
dc.identifier.pmid11320183
dc.identifier.urihttps://hdl.handle.net/2445/157305
dc.language.isoeng
dc.publisherLippincott, Williams & Wilkins. Wolters Kluwer Health
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1212/wnl.56.8.1084
dc.relation.ispartofNeurology, 2001, vol. 56, num. 8, p. 1084-1089
dc.relation.urihttps://doi.org/10.1212/wnl.56.8.1084
dc.rights(c) American Academy of Neurology, 2001
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.sourceArticles publicats en revistes (Medicina)
dc.subject.classificationHematopoesi
dc.subject.classificationCèl·lules mare
dc.subject.classificationLíquid cefalorraquidi
dc.subject.classificationEsclerosi múltiple
dc.subject.otherHematopoiesis
dc.subject.otherStem cells
dc.subject.otherCerebrospinal fluid
dc.subject.otherMultiple sclerosis
dc.titleMRI and CFS oligoclonal bands after autologus hematopoietic stem cell transplantation in MS
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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