dc.contributor.author
Boesl, Fabian
dc.contributor.author
Allers, Kristina
dc.contributor.author
Herm, Juliane
dc.contributor.author
Scheider, Thomas
dc.contributor.author
Franke, Christiana
dc.date.accessioned
2024-10-02T14:50:55Z
dc.date.available
2024-10-02T14:50:55Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/45127
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-44839
dc.description.abstract
Progressive multifocal leukoencephalopathy (PML) is a rare demyelinating disease of the CNS caused by the human polyomavirus 2 (JCV). PML predominantly occurs in immunocompromised patients. To date, no specific antiviral treatment exists, leaving only restoration of the immune system as possible treatment. In 2019, the monoclonal antibody pembrolizumab was reported as a potential treatment option in PML in a case series. Following case reports could not thoroughly confirm a positive outcome. Pembrolizumab targets the inhibitory programmed cell death protein 1 (PD-1) receptor on lymphocytes and is associated with beneficial expansion of pre-existing virus-specific T cells. Here we describe a patient with PML who benefited from combined treatment with intravenous immunoglobulins, maraviroc, and pembrolizumab.
en
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
Progressive multifocal leukoencephalopathy
en
dc.subject
Intravenous immunoglobulins
en
dc.subject
Pembrolizumab
en
dc.subject
Follicular lymphoma
en
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit
dc.title
Sequential treatment of progressive multifocal leukoencephalopathy with intravenous immunoglobulins and pembrolizumab
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.doi
10.1007/s13365-022-01059-2
dcterms.bibliographicCitation.journaltitle
Journal of NeuroVirology
dcterms.bibliographicCitation.number
2
dcterms.bibliographicCitation.originalpublishername
Springer Nature
dcterms.bibliographicCitation.pagestart
335
dcterms.bibliographicCitation.pageend
338
dcterms.bibliographicCitation.volume
28
refubium.affiliation
Charité - Universitätsmedizin Berlin
refubium.funding
Springer Nature DEAL
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.bibliographicCitation.pmid
35320511
dcterms.isPartOf.issn
1355-0284
dcterms.isPartOf.eissn
1538-2443