Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/109389
DC FieldValueLanguage
dc.contributor.authorCoimbra, Susana-
dc.contributor.authorFigueiredo, Américo-
dc.contributor.authorSantos-Silva, Alice-
dc.date.accessioned2023-10-12T08:58:22Z-
dc.date.available2023-10-12T08:58:22Z-
dc.date.issued2014-
dc.identifier.issn1555-1741pt
dc.identifier.urihttps://hdl.handle.net/10316/109389-
dc.description.abstractAdvances in knowledge regarding the pathogenesis of psoriasis have allowed the development of a new class of agents known as biologic drugs. Data confirm that T helper (Th)17 and interleukin (IL)-17 signaling has a crucial role in the pathogenesis of the disease. High levels of IL-17 and Th17-related cytokines have been reported in psoriasis, leading to the suggestion of agents targeting IL-17 as a potential therapeutic strategy in psoriasis. Brodalumab is a human monoclonal antibody that targets IL-17 receptor A, blocking the effects of IL-17A, IL-17F, and IL-17E. Data from Phase I and Phase II clinical trials indicate that brodalumab has a favorable safety and tolerability profile, with strong clinical activity, suggesting that it is a potential tool for use in the treatment of moderate-to-severe psoriasis.pt
dc.language.isoengpt
dc.publisherDove Medical Press Ltdpt
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/pt
dc.subjectinterleukin-17pt
dc.subjectinterleukin-17 receptorpt
dc.subjectmonoclonal antibodypt
dc.subjectT helper 17 pathwaypt
dc.titleBrodalumab: an evidence-based review of its potential in the treatment of moderate-to-severe psoriasispt
dc.typearticle-
degois.publication.firstPage89pt
degois.publication.lastPage97pt
degois.publication.titleCore Evidencept
dc.peerreviewedyespt
dc.identifier.doi10.2147/CE.S33940pt
degois.publication.volume9pt
dc.date.embargo2014-01-01*
uc.date.periodoEmbargo0pt
item.grantfulltextopen-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.openairetypearticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextCom Texto completo-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.orcid0000-0002-9105-9619-
Appears in Collections:FMUC Medicina - Artigos em Revistas Internacionais
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