The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
Autologous hematopoietic stem cell transplantation suppresses Gd-enhanced MRI activity in MS
Abstract
BACKGROUND: Autologous hematopoietic stem cell transplantation (ASCT) has been recently utilized with encouraging results in patients with poorly controlled MS. OBJECTIVE: To determine in severe cases of MS the effect of ASCT on gadolinium (Gd)-enhanced MRI and to obtain information on clinical course and safety. METHODS: In a cooperative study, 10 patients with rapidly evolving secondary progressive MS were transplanted, after BEAM conditioning regimen (carmustine, etoposide, cytosine-arabinoside, and melphalan), with unmanipulated autologous peripheral blood SC mobilized with high-dose cyclophosphamide (CY; 4 g/m2) and granulocyte-colony-stimulating factor. Triple-dose Gd-enhanced scans were performed monthly for a pretreatment period of 3 months and compared with serial monthly Gd-enhanced MRI for the following 6 months and then once every 3 months. RESULTS: The median follow-up is now 15 months (range 4 to 30 months). The number of Gd-enhancing lesions decreased immediately after mobilization with CY and finally dropped to zero in all cases after the conditioning regimen. The number of new T2-weighted positive lesions paralleled data obtained for Gd-enhanced MRI. Clinically, patients improved slightly or remained stable. CONCLUSION: These results demonstrate that the therapeutic sequence CY-BEAM-ASCT has the capacity to completely suppress MR-enhancing activity, an effect that is sustained with time. The final impact of this procedure on disease course remains to be established.
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Cites
Axonal transection in the lesions of multiple sclerosis
Trapp, B. D., Peterson, J., Ransohoff, R. M., Rudick, R., Mörk, S., & Bö, L. (1998) · New England Journal of Medicine · doi:10.1056/nejm199801293380502 · Cited by 4,029
Kappos, L., Moeri, D., Radue, E. W., Schoetzau, A., Schweikert, K., Barkhof, F., Miller, D., Guttmann, C. R., Weiner, H. L., Gasperini, C., et al. (1999) · The Lancet · doi:10.1016/s0140-6736(98)03053-0 · Cited by 499
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Immunology of multiple sclerosis
Sospedra, M., & Martin, R. (2005) · Annual Review of Immunology · doi:10.1146/annurev.immunol.23.021704.115707 · Cited by 2,149
Muraro, P. A., Douek, D. C., Packer, A., Chung, K., Guenaga, F. J., Cassiani-Ingoni, R., Campbell, C., Memon, S., Nagle, J. W., Hakim, F. T., et al. (2005) · The Journal of Experimental Medicine · doi:10.1084/jem.20041679 · Cited by 502
Autologous haematopoietic stem cell transplantation for treatment of multiple sclerosis
Muraro, P. A., Martin, R., Mancardi, G. L., Nicholas, R., Sormani, M. P., & Saccardi, R. (2017) · Nature Reviews Neurology · doi:10.1038/nrneurol.2017.81 · Cited by 304
Self-citationStem cell therapy in amyotrophic lateral sclerosis: a methodological approach in humans
Mazzini, L., Fagioli, F., Boccaletti, R., Mareschi, K., Oliveri, G., Olivieri, C., Pastore, I., Marasso, R., & Madon, E. (2003) · Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders · doi:10.1080/14660820310014653 · Cited by 256
Metadata
- Authors
- Mancardi, G. L., Saccardi, R., Filippi, M., Gualandi, F., Murialdo, A., Inglese, M., Marrosu, M. G., Meucci, G., Massacesi, L., Lugaresi, A., Pagliai, F., Sormani, M. P., Sardanelli, F., Marmont, A., & Sclerosis*, T. I. G.-N. I. O. A. H. S. C. T. F. M.
- Venue
- Neurology
- Published
- 2001-07-10
- Volume
- 57
- Issue
- 1
- Pages
- 62-68
- ISSN
- 0028-3878 (ISSN-L)
- 1526-632X
- OpenAlex
- W1978703555
- Cited by
- 168
- References
- 2
- FWCI
- 9.14
- Type
- journal article
- Language
- en
- Open access
- closed
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- Mancardi, G. L., Saccardi, R., Filippi, M., Gualandi, F., Murialdo, A., Inglese, M., Marrosu, M. G., Meucci, G., Massacesi, L., Lugaresi, A., Pagliai, F., Sormani, M. P., Sardanelli, F., Marmont, A., & Sclerosis*, T. I. G.-N. I. O. A. H. S. C. T. F. M. (2001). Autologous hematopoietic stem cell transplantation suppresses Gd-enhanced MRI activity in MS. Neurology. https://doi.org/10.1212/wnl.57.1.62
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