2021
DOI: 10.1111/ddg.14612
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Alleviation of erosive oral and esophageal lichen planus by the JAK1 inhibitor upadacitinib

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Cited by 20 publications
(19 citation statements)
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“…In OLP the use of JAKI is limited to case reports. Three OLP patients were successfully treated with JAKI, one of them with baricitinib and two others with upadacitinib ( 64 66 ).…”
Section: Janus Kinases Inhibitorsmentioning
confidence: 99%
“…In OLP the use of JAKI is limited to case reports. Three OLP patients were successfully treated with JAKI, one of them with baricitinib and two others with upadacitinib ( 64 66 ).…”
Section: Janus Kinases Inhibitorsmentioning
confidence: 99%
“…The JAK inhibitors mentioned can be divided into two groups: baricitinib, delgocitinib, ruxolitinib and tofacitinib may be referred to as the alpha group of JAK inhibitors; these exhibit structural similarities and have a broader pharmacological binding selectivity than representatives of the beta group (abrocitinib, deucravacitinib, filgotinib, upadacitinib). Given the ubiquity of the JAK/STAT signaling pathway and its involvement in many regulatory mechanisms, especially in inflammatory processes, the use of various JAK inhibitors has been considered or already examined in clinical trials for many chronic inflammatory diseases involving the skin [44][45][46][47]. The most comprehensive data are available for indications of atopic dermatitis [38,48,49], psoriasis and psoriatic arthritis [34,50], alopecia areata [51][52][53], hand eczema [54] and vitiligo [55].…”
Section: Inhibitors Of Janus Kinasesmentioning
confidence: 99%
“…Case reports described good outcomes of LP under therapy with the JAK1/3 inhibitor tofacitinib [7][8][9]. Recently, a good therapeutic response of a patient with erosive oral and esophageal LP treated with upadacitinib, a preferential JAK1 inhibitor, was described [15], suggesting that not only the dual inhibition of JAK1 and JAK3, but also a predominant inhibition of JAK1 may be sufficient as therapy of oral LP. Clinical data on inhibition of JAK2 and TYK2 in patients with LP are to the best of our knowledge not available so far.…”
Section: Clinical Lettermentioning
confidence: 99%