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A Case of Immunoglobulin G4-related Disease Complicated by Atopic Dermatitis Responsive to Upadacitinib Treatment.
Kusaka, Katsuhide; Nakayamada, Shingo; Hanami, Kentaro; Nawata, Aya; Tanaka, Yoshiya.
Afiliação
  • Kusaka K; Department of Internal Medicine, University of Occupational and Environmental Health, Japan, Fukuoka, Japan.
  • Nakayamada S; Department of Internal Medicine, University of Occupational and Environmental Health, Japan, Fukuoka, Japan.
  • Hanami K; Department of Internal Medicine, University of Occupational and Environmental Health, Japan, Fukuoka, Japan.
  • Nawata A; Department of Internal Medicine, University of Occupational and Environmental Health, Japan, Fukuoka, Japan.
  • Tanaka Y; Department of Internal Medicine, University of Occupational and Environmental Health, Japan, Fukuoka, Japan.
Article em En | MEDLINE | ID: mdl-39177378
ABSTRACT
Immunoglobulin G4-related disease is mainly treated with glucocorticoids. In many cases, this disease is resistant to glucocorticoids, and their toxicity can be a problem. We encountered a patient with immunoglobulin G4-related disease affecting multiple organs (such as the skin, lung, and lacrimal gland), who had comorbidities, including atopic dermatitis and diabetes. In this case, while glucocorticoid tapering was difficult, the introduction of upadacitinib resulted in remission of both atopic dermatitis and immunoglobulin G4-related disease without glucocorticoid dose escalation. Peripheral blood flow cytometry analysis showed that the proportions of activated non Th1/Th17 cells subset (Th2 cells), follicular helper T cells, and plasmocytes were increased before upadacitinib therapy but all normalised after treatment. Interleukin-4 and interleukin-21 signals are important for the differentiation of CD4+ T cells into type 2 helper T or B cells in the peripheral blood. Our case suggested that inhibition of Janus kinase 1, which mediates these signals, might have contributed to improved pathological conditions in immunoglobulin G4-related disease.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article