Filling the gaps in generalized pustular psoriasis: Role of IL-36R antibodies
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Filling the gaps in generalized pustular psoriasis : Role of IL-36R antibodies. / Nielsen, V. W.; Thomsen, S. F.
I: Drugs of the Future, Bind 46, Nr. 12, 12.2021, s. 995-1002.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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TY - JOUR
T1 - Filling the gaps in generalized pustular psoriasis
T2 - Role of IL-36R antibodies
AU - Nielsen, V. W.
AU - Thomsen, S. F.
N1 - Publisher Copyright: © 2021 Clarivate.
PY - 2021/12
Y1 - 2021/12
N2 - Generalized pustular psoriasis (GPP) is a rare skin disorder that presents with flares of extensive sterile pustules. No GPP-specific treatment has been approved in the U.S. or Europe, and the lack of universal guidelines complicates the treatment of this debilitating disease. Recently, the pathophysiology of GPP has been attributed to overactivation of the interleukin-36 (IL-36) signaling pathway, due to loss-of-function mutations uncovered in the gene encoding the IL-36 receptor antagonist. The IL-36 receptor has therefore become a promising target for therapeutic intervention, with early studies of anti-IL-36R treatment, namely spesolimab and imsidolimab, demonstrating rapid inhibition of the IL-36 signaling pathway and improvement of disease symptoms. Both treatments were well tolerated with no serious adverse events reported, making anti-IL-36R treatment a promising addition to the sparse therapeutic options currently available.
AB - Generalized pustular psoriasis (GPP) is a rare skin disorder that presents with flares of extensive sterile pustules. No GPP-specific treatment has been approved in the U.S. or Europe, and the lack of universal guidelines complicates the treatment of this debilitating disease. Recently, the pathophysiology of GPP has been attributed to overactivation of the interleukin-36 (IL-36) signaling pathway, due to loss-of-function mutations uncovered in the gene encoding the IL-36 receptor antagonist. The IL-36 receptor has therefore become a promising target for therapeutic intervention, with early studies of anti-IL-36R treatment, namely spesolimab and imsidolimab, demonstrating rapid inhibition of the IL-36 signaling pathway and improvement of disease symptoms. Both treatments were well tolerated with no serious adverse events reported, making anti-IL-36R treatment a promising addition to the sparse therapeutic options currently available.
KW - ANB-019
KW - Generalized pustular psoriasis
KW - IL-36 receptor antibody
KW - IL36RN
KW - Imsidolimab
KW - Spesolimab
U2 - 10.1358/dof.2021.46.12.3331003
DO - 10.1358/dof.2021.46.12.3331003
M3 - Journal article
AN - SCOPUS:85122241625
VL - 46
SP - 995
EP - 1002
JO - Drugs of the Future
JF - Drugs of the Future
SN - 0377-8282
IS - 12
ER -
ID: 290181499