Publication:
Treatment of alopecia areata partim universalis with efalizumab

cris.virtualsource.author-orcid964bc10d-9d83-4aa4-9760-e8cb69ed562f
cris.virtualsource.author-orcid657eb181-3137-4b10-9226-937f459da4de
datacite.rightsmetadata.only
dc.contributor.authorKaelin, Ursula
dc.contributor.authorHassan, Akmhal Said
dc.contributor.authorBraathen, Lasse Roger
dc.contributor.authorYawalkar, Nikhil
dc.date.accessioned2024-10-13T13:34:32Z
dc.date.available2024-10-13T13:34:32Z
dc.date.issued2006
dc.description.abstractAlopecia areata (AA) is considered an autoimmune disease targeted at hair follicles with T-lymphocytes playing an important role in the pathogenesis. Treatment of AA, particularly the totalis and universalis subtypes, is often difficult and remains a therapeutic challenge. Novel biologic therapies that have been developed for the treatment of other immune-mediated inflammatory skin diseases may represent a new therapeutic modality for this disease. Efalizumab is a humanized monoclonal anti-CD11a antibody that inhibits T-cell activation and migration. We report a case of a 19-year-old man suffering from AA partim universalis, treated with efalizumab monotherapy. The treatment was well tolerated with no reported side effects. The striking improvement warrants further studies with this biologic therapy in AA.
dc.description.numberOfPages4
dc.description.sponsorshipUniversitätsklinik für Dermatologie
dc.identifier.isi000240040200029
dc.identifier.pmid16908369
dc.identifier.publisherDOI10.1016/j.jaad.2006.05.062
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/92673
dc.language.isoen
dc.publisherElsevier
dc.publisher.placeNew York, N.Y.
dc.relation.isbn16908369
dc.relation.ispartofJournal of the American Academy of Dermatology
dc.relation.issn0190-9622
dc.relation.organizationDCD5A442BAD9E17DE0405C82790C4DE2
dc.titleTreatment of alopecia areata partim universalis with efalizumab
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage32
oaire.citation.issue3
oaire.citation.startPage529
oaire.citation.volume55
oairecerif.author.affiliationUniversitätsklinik für Dermatologie
oairecerif.author.affiliationUniversitätsklinik für Dermatologie
unibe.contributor.rolecreator
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unibe.contributor.rolecreator
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unibe.description.ispublishedpub
unibe.eprints.legacyId18893
unibe.journal.abbrevTitleJ AM ACAD DERMATOL
unibe.subtype.articlecontribution

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