Logo: to the web site of Uppsala University

uu.sePublications from Uppsala University
Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
Autologous hematopoietic stem cell transplantation for pediatric autoimmune neurologic disorders
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Medical Sciences, Translationell Neurology.ORCID iD: 0000-0002-7045-1806
2024 (English)In: Handbook of Clinical Neurology: Hematopoietic Stem Cell Transplantation for Neurologic Diseases / [ed] Matilde Inglese; Giovanni L. Mancardi, Amsterdam; London; Cambridge: Elsevier, 2024, Vol. 202, p. 249-258, article id B978-0-323-90242-7.00004-3Chapter in book (Refereed)
Abstract [en]

Autologous hematopoietic stem cell transplantation (aHSCT) may be effective in carefully selected pediatric patients with multiple sclerosis (MS), neuromyelitis optica (NMO), and chronic inflammatory demyelinating polyneuropathy (CIDP). aHSCT for pediatric MS (same as for adults) is performed to eradicate inflammatory autoreactive cells with lympho-ablative regimens and restore immune tolerance. Its therapeutic effect in MS relies on various mechanisms: (1) the immunosuppressive conditioning regimen prior to aHSCT was able to eradicate the autoreactive cells and (2) the regeneration/renewal of the immune system to reset the aberrant immune response against self-antigens. The aHSCT procedure includes the following different steps, as described in this chapter: patient selection through careful pretransplant screening, “wash-out” period from previous treatments, mobilization of hematopoietic stem cells (HSC), conditioning regimen, HSC infusion, and posttransplant monitoring for early and late complications. Moreover, specific aspects of pediatric population undergoing aHSCT are described.

According to the available evidence, aHSCT appears to be safe in pediatric MS, obtaining disease control for a prolonged time after the procedure. A reasonable approach in this setting includes the application of less toxic treatments while reserving aHSCT procedure for patients with severe/refractory forms of the disease. The EBMT considers MS, NMO, and CIDP in pediatric patients within the category of the clinical option (CO), where candidates for aHSCT can be selected on the basis of careful consideration of individual case history in the multidisciplinary setting.

Place, publisher, year, edition, pages
Amsterdam; London; Cambridge: Elsevier, 2024. Vol. 202, p. 249-258, article id B978-0-323-90242-7.00004-3
Series
Handbook of clinical neurology, ISSN 0072-9752, E-ISSN 2212-4152 ; 202
Keywords [en]
Autoimmune disorders, Children, Hematopoietic stem cell transplantation, Multiple sclerosis
National Category
Neurology
Research subject
Medical Science
Identifiers
URN: urn:nbn:se:uu:diva-548659DOI: 10.1016/B978-0-323-90242-7.00004-3PubMedID: 39111911Scopus ID: 2-s2.0-85200332639ISBN: 978-0-323-90242-7 (print)OAI: oai:DiVA.org:uu-548659DiVA, id: diva2:1931869
Available from: 2025-01-28 Created: 2025-01-28 Last updated: 2025-01-30Bibliographically approved

Open Access in DiVA

No full text in DiVA

Other links

Publisher's full textPubMedScopus

Authority records

Burman, Joachim

Search in DiVA

By author/editor
Burman, Joachim
By organisation
Translationell Neurology
Neurology

Search outside of DiVA

GoogleGoogle Scholar

doi
pubmed
isbn
urn-nbn

Altmetric score

doi
pubmed
isbn
urn-nbn
Total: 70 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf