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Thymus and Activation-regulated Chemokine as a Biomarker for IgG4-related Disease.
Umeda, Masataka; Origuchi, Tomoki; Kawashiri, Shin-Ya; Koga, Tomohiro; Ichinose, Kunihiro; Furukawa, Kaori; Sato, Tomohito; Tsuji, Sousuke; Endo, Yushiro; Takatani, Ayuko; Shimizu, Toshimasa; Fukui, Shoichi; Iwamoto, Naoki; Igawa, Takashi; Tamai, Mami; Nakamura, Hideki; Kawakami, Atsushi.
Afiliação
  • Umeda M; Department of Immunology and Rheumatology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan. masatakau0807@gmail.com.
  • Origuchi T; Medical Education Development Center, Nagasaki University Hospital, Nagasaki, Japan. masatakau0807@gmail.com.
  • Kawashiri SY; Department of Locomotive Rehabilitation, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki, Japan. origuchi@nagasaki-u.ac.jp.
  • Koga T; Department of Immunology and Rheumatology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
  • Ichinose K; Departments of Community Medicine, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
  • Furukawa K; Department of Immunology and Rheumatology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
  • Sato T; Center for Bioinformatics and Molecular Medicine, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
  • Tsuji S; Department of Immunology and Rheumatology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
  • Endo Y; Department of Immunology and Rheumatology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
  • Takatani A; Department of Immunology and Rheumatology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
  • Shimizu T; Department of Immunology and Rheumatology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
  • Fukui S; Department of Immunology and Rheumatology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
  • Iwamoto N; Department of Immunology and Rheumatology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
  • Igawa T; Department of Immunology and Rheumatology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
  • Tamai M; Department of Immunology and Rheumatology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
  • Nakamura H; Department of Immunology and Rheumatology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
  • Kawakami A; Department of Immunology and Rheumatology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
Sci Rep ; 10(1): 6010, 2020 04 07.
Article em En | MEDLINE | ID: mdl-32265499
High serum concentrations of thymus and activation-regulated chemokine (TARC) are observed in allergic diseases such as atopic dermatitis and bronchial asthma. Frequent allergic symptoms have been reported in patients with IgG4-related disease (IgG4-RD). We investigated the pathogenic role of TARC as a biomarker in IgG4-RD patients. We evaluated the serum concentrations of TARC from 29 IgG4-RD patients, 28 primary Sjögren syndrome (pSS) patients, and 23 healthy controls (HCs) by enzyme-linked immunosorbent assay (ELISA). We analyzed the correlations between the TARC concentrations and the subjects' clinical parameters. To investigate the biological effect of TARC on the pathogenesis of IgG4-RD, we evaluated the in vitro induction of plasmablasts from IgG4-RD patients by TARC. The serum concentrations of TARC in the IgG4-RD patients were significantly higher than those of the pSS patients and HCs. The serum TARC concentration of the IgG4-RD group was positively correlated with the IgG4-RD responder index (IgG4-RD RI) score and with the number of organs involved, but it was not correlated with the serum IgG4 level or eosinophil number in the IgG4-RD patients' peripheral blood. The patients who had lung involvement had higher serum TARC concentrations. In vitro, TARC clearly induced the formation of plasmablasts from the IgG4-RD patients' peripheral blood mononuclear cells. Collectively, our data suggest that a systemic increment of TARC may contribute to the development of IgG4-RD through an aberrant induction of plasmablasts.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Quimiocina CCL17 / Doença Relacionada a Imunoglobulina G4 Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Quimiocina CCL17 / Doença Relacionada a Imunoglobulina G4 Idioma: En Ano de publicação: 2020 Tipo de documento: Article