Long-lasting severe anemia following treatment with natalizumab for relapsing-remitting multiple sclerosis: a case report.


Journal

Journal of medical case reports
ISSN: 1752-1947
Titre abrégé: J Med Case Rep
Pays: England
ID NLM: 101293382

Informations de publication

Date de publication:
13 May 2024
Historique:
received: 10 01 2024
accepted: 15 04 2024
medline: 13 5 2024
pubmed: 13 5 2024
entrez: 12 5 2024
Statut: epublish

Résumé

Natalizumab is a monoclonal antibody used to treat patients with relapsing-remitting multiple sclerosis. Anemia is a recognized side effect, but it is usually mild and of a short duration when natalizumab is stopped. Here, we describe a case of a young woman with severe and especially long lasting anemia associated with treatment with natalizumab, persisting up to a year after treatment was stopped. A 24 year-old Caucasian woman with relapsing-remitting multiple sclerosis developed severe transfusion dependent anemia after 27 infusions with natalizumab, which was her first and only treatment for her multiple sclerosis. Extensive hematologic diagnostics did not reveal any malignant cause or any other plausible non-malignant cause for her anemia. The bone marrow was found to be hypercellular, with a maturation arrest of the erythropoiesis and with grade 1-2 fibrosis. No specific treatment for the anemia was given. The hemoglobin level showed signs of spontaneous increase after nearly one year after natalizumab was discontinued. Severe anemia can be caused by treatment with natalizumab. This case adds information to the few other similar reported cases, demonstrating the potential duration of the anemia, as well as detailed description of hematologic findings. The mechanism is most likely due to inhibition of α4 subunit of the α4β1-integrin, which is present on both lymphocytes and erythroid precursor cells.

Sections du résumé

BACKGROUND BACKGROUND
Natalizumab is a monoclonal antibody used to treat patients with relapsing-remitting multiple sclerosis. Anemia is a recognized side effect, but it is usually mild and of a short duration when natalizumab is stopped. Here, we describe a case of a young woman with severe and especially long lasting anemia associated with treatment with natalizumab, persisting up to a year after treatment was stopped.
CASE PRESENTATION METHODS
A 24 year-old Caucasian woman with relapsing-remitting multiple sclerosis developed severe transfusion dependent anemia after 27 infusions with natalizumab, which was her first and only treatment for her multiple sclerosis. Extensive hematologic diagnostics did not reveal any malignant cause or any other plausible non-malignant cause for her anemia. The bone marrow was found to be hypercellular, with a maturation arrest of the erythropoiesis and with grade 1-2 fibrosis. No specific treatment for the anemia was given. The hemoglobin level showed signs of spontaneous increase after nearly one year after natalizumab was discontinued.
CONCLUSION CONCLUSIONS
Severe anemia can be caused by treatment with natalizumab. This case adds information to the few other similar reported cases, demonstrating the potential duration of the anemia, as well as detailed description of hematologic findings. The mechanism is most likely due to inhibition of α4 subunit of the α4β1-integrin, which is present on both lymphocytes and erythroid precursor cells.

Identifiants

pubmed: 38736000
doi: 10.1186/s13256-024-04562-8
pii: 10.1186/s13256-024-04562-8
doi:

Substances chimiques

Natalizumab 0
Immunologic Factors 0

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

245

Informations de copyright

© 2024. The Author(s).

Références

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Auteurs

Lars Henrik Dahl Hamnvik (LHD)

Department of Medicine, Drammen Hospital, Vestre Viken Trust, Drammen, Norway. lahdah@vestreviken.no.
Department of Haematology, Oslo University Hospital, Oslo, Norway. lahdah@vestreviken.no.

Geir E Tjønnfjord (GE)

Department of Haematology, Oslo University Hospital, Oslo, Norway.
Institute of Clinical Medicine, KG Jebsen Centre for B-Cell Malignancies, University of Oslo, Oslo, Norway.

Signe Spetalen (S)

Department of Pathology, Oslo University Hospital, Oslo, Norway.

Jakob Dalgaard (J)

Department of Medicine, Drammen Hospital, Vestre Viken Trust, Drammen, Norway.

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