Bullous pemphigoid is a devastating autoimmune blistering disease with need for improved therapeutics. Limited data are available on the overall burden of pruritus and alterations over time; however, treatment of itch-specific pathways may provide novel therapeutics. In this paper, we analyzed the QOL impact particularly related to itch and determined corresponding changes in intraepidermal nerve fiber density and gene expression. A total of 43 patients with bullous pemphigoid were followed prospectively on standard-of-care treatment and showed average Bullous Pemphigoid Disease Area Index total activity score decrease from 19.1 ± 19.2 to 8.2 ± 11.3 and improvement in QOL measures Autoimmune Bullous Disease Quality of Life, Treatment of Autoimmune Bullous Disease Quality of Life, and ItchyQoL. At baseline, intraepidermal nerve fiber density in patients with bullous pemphigoid and atopic dermatitis were significantly lower than in healthy controls (7.3 ± 1.5 and 3.2 ± 2.0 vs 9.7 ± 5.4 fibers/mm, = .031) and increased from baseline to follow-up visit (11.7 ± 0.4 and 5.8 ± 2.7), although only atopic dermatitis reached statistical significance ( = .018). , , , and genes were highly upregulated in the skin of patients with bullous pemphigoid compared with those in healthy controls. Our data provide evidence for improvements in itch-related QOL over time on standard-of-care therapies with unique alterations in inflammatory mediators related to early immune cell activation and recruitment.
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http://dx.doi.org/10.1016/j.xjidi.2024.100329 | DOI Listing |
J Am Acad Dermatol
March 2025
Department of Dermatology, Rutgers Robert Wood Johnson Medical School, Somerset, NJ; Department of Dermatology, Weill Cornell School of Medicine, New York, NY.
Gan To Kagaku Ryoho
February 2025
Dept. of Surgery, Kaizuka City Hospital.
The patient is a 66-year-old man. He underwent a total of 9 courses of GCD therapy(gemcitabine+cisplatin+durvalumab)for intrahepatic cholangiocarcinoma with direct invasion of the greater omentum and abdominal wall and surrounding peritoneal dissemination. The tumor had shrunk and was judged to be curative, and laparoscopic hepatic S4a/S5 subsegmentectomy and S6 partial hepatectomy were performed at 8 months after the initial diagnosis.
View Article and Find Full Text PDFArch Dermatol Res
March 2025
Autoimmune Bullous Diseases Research Center, Razi Hospital, Tehran University of Medical Sciences, Tehran, 1199663911, Iran.
Bullous pemphigoid (BP) is the most common autoimmune-driven blistering disease. The incidence of BP has been rising due to population aging and exposure to medications such as biologics. Moreover, biologics are utilized as therapeutic choices for BP treatment as they inhibit cytokines and disrupt pathogenesis pathways.
View Article and Find Full Text PDFJ Eur Acad Dermatol Venereol
March 2025
2nd Department of Dermatology and Venereology, Papageorgiou General Hospital of Thessaloniki, Aristotle University School of Medicine, Thessaloniki, Greece.
Am J Clin Dermatol
March 2025
Hospital for Skin Diseases, Shandong First Medical University, Jinan, Shandong Province, China.
Background: There are limited data on clinical outcomes and prognosis factors for bullous pemphigoid (BP) at long-term follow-up.
Objective: We aimed to investigate the clinical outcomes and prognostic factors in BP patients.
Methods: This retrospective study was performed between January 1, 2009 and December 31, 2023 in Shandong Province, China.
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