Severe meningo-/encephalitis after daclizumab therapy for multiple sclerosis.


Journal

Multiple sclerosis (Houndmills, Basingstoke, England)
ISSN: 1477-0970
Titre abrégé: Mult Scler
Pays: England
ID NLM: 9509185

Informations de publication

Date de publication:
10 2019
Historique:
pubmed: 19 1 2019
medline: 1 7 2020
entrez: 19 1 2019
Statut: ppublish

Résumé

Daclizumab is a monoclonal antibody that binds the high-affinity interleukin-2 receptor and was approved for the treatment of relapsing multiple sclerosis. Due to severe inflammatory brain disorders, the approval was suspended in March 2018. This retrospective cohort study summarizes clinical, laboratory, radiological, and histological findings of seven patients who developed meningo-/encephalitis after daclizumab therapy. Patients presented with encephalitis and/or meningitis and suffered from systemic symptoms such as fever (5/7), exanthema (5/7), or gastrointestinal symptoms (4/7). Secondary autoimmune diseases developed. Blood analysis revealed an increase in eosinophils (5/7). Six patients fulfilled the diagnostic criteria for a drug reaction with eosinophilia and systemic symptoms (DRESS). Magnetic resonance imaging (MRI) showed multiple contrast-enhancing lesions, and enhancement of the ependyma (6/7), meninges (5/7), cranial or spinal nerves (2/7), and a vasculitic pattern (3/7). Histology revealed a pronounced inflammatory infiltrate consisting of lymphocytes, plasma cells and eosinophils, and densely infiltrated vessels. Most patients showed an insufficient therapeutic response and a high disability at last follow-up (median Expanded Disability Status Scale (EDSS) 8). Two patients died. Meningoencephalitis and DRESS may occur with daclizumab therapy. This potential lethal side effect is characterized by a dysregulated immune response. Our findings underline the importance of postmarketing drug surveillance.

Sections du résumé

BACKGROUND
Daclizumab is a monoclonal antibody that binds the high-affinity interleukin-2 receptor and was approved for the treatment of relapsing multiple sclerosis. Due to severe inflammatory brain disorders, the approval was suspended in March 2018.
OBJECTIVE AND METHODS
This retrospective cohort study summarizes clinical, laboratory, radiological, and histological findings of seven patients who developed meningo-/encephalitis after daclizumab therapy.
RESULTS
Patients presented with encephalitis and/or meningitis and suffered from systemic symptoms such as fever (5/7), exanthema (5/7), or gastrointestinal symptoms (4/7). Secondary autoimmune diseases developed. Blood analysis revealed an increase in eosinophils (5/7). Six patients fulfilled the diagnostic criteria for a drug reaction with eosinophilia and systemic symptoms (DRESS). Magnetic resonance imaging (MRI) showed multiple contrast-enhancing lesions, and enhancement of the ependyma (6/7), meninges (5/7), cranial or spinal nerves (2/7), and a vasculitic pattern (3/7). Histology revealed a pronounced inflammatory infiltrate consisting of lymphocytes, plasma cells and eosinophils, and densely infiltrated vessels. Most patients showed an insufficient therapeutic response and a high disability at last follow-up (median Expanded Disability Status Scale (EDSS) 8). Two patients died.
CONCLUSION
Meningoencephalitis and DRESS may occur with daclizumab therapy. This potential lethal side effect is characterized by a dysregulated immune response. Our findings underline the importance of postmarketing drug surveillance.

Identifiants

pubmed: 30657420
doi: 10.1177/1352458518819098
doi:

Substances chimiques

Antibodies, Monoclonal 0
Immunosuppressive Agents 0
Daclizumab CUJ2MVI71Y

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1618-1632

Commentaires et corrections

Type : CommentIn

Auteurs

Lidia Stork (L)

Institute of Neuropathology, University Medical Center Göttingen, Göttingen, Germany.

Wolfgang Brück (W)

Institute of Neuropathology, University Medical Center Göttingen, Göttingen, Germany.

Phillip von Gottberg (P)

Institute of Neuroradiology, University Medical Center Göttingen, Göttingen, Germany.

Ulrich Pulkowski (U)

Department of Neurology, Imland Hospital, Rendsburg, Germany.

Florian Kirsten (F)

Department of Neurology, Imland Hospital, Rendsburg, Germany.

Markus Glatzel (M)

Institute of Neuropathology, University Hospital Hamburg Eppendorf, Hamburg, Germany.

Sebastian Rauer (S)

Department of Neurology, University Medical Center Freiburg, Freiburg, Germany.

Franziska Scheibe (F)

Department of Neurology, Charité-Universitätsmedizin Berlin, Berlin, Germany.

Helena Radbruch (H)

Institute of Neuropathology, Charité-Universitätsmedizin Berlin, Berlin, Germany.

Eckhard Hammer (E)

Department of Neurology, Marienkrankenhaus, Hamburg, Germany.

Klarissa H Stürner (KH)

Department of Neurology, University Hospital Schleswig-Holstein, Kiel, Germany.

Barbara Kaulen (B)

Department of Neurology, University Hospital Hamburg Eppendorf, Hamburg, Germany; Institute of Neuroimmunology and Multiple Sclerosis, University Hospital Hamburg Eppendorf, Hamburg, Germany.

Christoph Heesen (C)

Department of Neurology, University Hospital Hamburg Eppendorf, Hamburg, Germany; Institute of Neuroimmunology and Multiple Sclerosis, University Hospital Hamburg Eppendorf, Hamburg, Germany.

Frank Hoffmann (F)

Department of Neurology, Martha-Maria Hospital, Halle, Germany.

Sebastian Brock (S)

Department of Neurology, Martha-Maria Hospital, Halle, Germany.

Marc Pawlitzki (M)

Department of Neurology, University Medical Center, Otto von Guericke University, Magdeburg, Germany.

Tobias Bopp (T)

Institute for Immunology, University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany.

Imke Metz (I)

Institute of Neuropathology, University Medical Center Göttingen, Göttingen, Germany.

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Classifications MeSH