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Prognostic Role of Interferon-λ3 in Anti-Melanoma Differentiation-Associated Gene 5-Positive Dermatomyositis-Associated Interstitial Lung Disease.
Fukada, Atsuki; Fujisawa, Tomoyuki; Hozumi, Hironao; Koda, Keigo; Akamatsu, Taisuke; Oyama, Yoshiyuki; Satake, Yasuomi; Niwa, Mitsuru; Kaida, Yusuke; Matsuda, Hiroyuki; Yokomura, Koshi; Koshimizu, Naoki; Toyoshima, Mikio; Imokawa, Shiro; Hashimoto, Dai; Yoshida, Akira; Gono, Takahisa; Kuwana, Masataka; Yamano, Yasuhiko; Kondoh, Yasuhiro; Yamashita, Keita; Maekawa, Masato; Mori, Kazutaka; Inoue, Yusuke; Yasui, Hideki; Suzuki, Yuzo; Karayama, Masato; Furuhashi, Kazuki; Enomoto, Noriyuki; Inui, Naoki; Suda, Takafumi.
Affiliation
  • Fukada A; Hamamatsu University School of Medicine, Hamamatsu, Japan.
  • Fujisawa T; Hamamatsu University School of Medicine, Hamamatsu, Japan.
  • Hozumi H; Hamamatsu University School of Medicine, Hamamatsu, Japan.
  • Koda K; Hamamatsu Rosai Hospital, Hamamatsu, Japan.
  • Akamatsu T; Shizuoka General Hospital, Shizuoka, Japan.
  • Oyama Y; Shizuoka Saiseikai General Hospital, Shizuoka, Japan.
  • Satake Y; Shizuoka City Shizuoka Hospital, Shizuoka, Japan.
  • Niwa M; Hamamatsu Medical Center, Hamamatsu, Japan.
  • Kaida Y; Enshu Hospital, Hamamatsu, Japan.
  • Matsuda H; Japanese Red Cross Shizuoka Hospital, Shizuoka, Japan.
  • Yokomura K; Seirei Mikatahara General Hospital, Hamamatsu, Japan.
  • Koshimizu N; Fujieda Municipal General Hospital, Fujieda, Japan.
  • Toyoshima M; Hamamatsu Rosai Hospital, Hamamatsu, Japan.
  • Imokawa S; Iwata City Hospital, Iwata, Japan.
  • Hashimoto D; Seirei Hamamatsu General Hospital, Hamamatsu, Japan.
  • Yoshida A; Nippon Medical School Graduate School of Medicine, Tokyo, Japan.
  • Gono T; Nippon Medical School Graduate School of Medicine, Tokyo, Japan.
  • Kuwana M; Nippon Medical School Graduate School of Medicine, Tokyo, Japan.
  • Yamano Y; Tosei General Hospital, Seto, Japan.
  • Kondoh Y; Tosei General Hospital, Seto, Japan.
  • Yamashita K; Hamamatsu University School of Medicine, Hamamatsu, Japan.
  • Maekawa M; Hamamatsu University School of Medicine, Hamamatsu, Japan.
  • Mori K; Shizuoka City Shimizu Hospital, Shizuoka, Japan.
  • Inoue Y; Hamamatsu University School of Medicine, Hamamatsu, Japan.
  • Yasui H; Hamamatsu University School of Medicine, Hamamatsu, Japan.
  • Suzuki Y; Hamamatsu University School of Medicine, Hamamatsu, Japan.
  • Karayama M; Hamamatsu University School of Medicine, Hamamatsu, Japan.
  • Furuhashi K; Hamamatsu University School of Medicine, Hamamatsu, Japan.
  • Enomoto N; Hamamatsu University School of Medicine, Hamamatsu, Japan.
  • Inui N; Hamamatsu University School of Medicine, Hamamatsu, Japan.
  • Suda T; Hamamatsu University School of Medicine, Hamamatsu, Japan.
Arthritis Rheumatol ; 76(5): 796-805, 2024 May.
Article in En | MEDLINE | ID: mdl-38146102
ABSTRACT

OBJECTIVE:

Interferon-λ3 (IFNλ3) is a cytokine with antiviral functions on barrier surfaces, and it is associated with disease activity in autoimmune diseases. This study assessed the clinical significance of serum IFNλ3 levels in polymyositis/dermatomyositis (PM/DM)-associated interstitial lung disease (ILD).

METHODS:

We measured serum IFNλ3 levels in 221 patients with PM/DM-ILD (155 in the derivation cohort, 66 in the validation cohort) and 38 controls. We evaluated factors associated with mortality risk among 79 patients with anti-melanoma differentiation-associated gene 5 (MDA5) antibody-positive DM-ILD.

RESULTS:

Serum IFNλ3 levels at diagnosis were significantly higher in patients with PM/DM-ILD than in healthy controls. Remarkably, serum IFNλ3 levels were specifically increased in patients with anti-MDA5 antibody-positive DM-ILD in both the derivation and validation cohorts. In anti-MDA5 antibody-positive DM-ILD, patients with high IFNλ3 levels (>120 pg/mL) had significantly lower survival rates than those with low IFNλ3 levels (≤120 pg/mL). A multivariate analysis revealed that high IFNλ3 levels, as well as old age and low Pao2, were significantly associated with poor prognoses in patients with anti-MDA5 antibody-positive DM-ILD. In a classification analysis of patients with anti-MDA5 antibody-positive DM-ILD based on age, IFNλ3 level, and Pao2, patients with old age (>53 years), high IFNλ3 levels (>120 pg/mL), and low Pao2 (<75 mm Hg) had the worst survival. In lung pathologic analyses, IFNλ3-positive staining was observed in macrophages, airway epithelial cells, the pleural region, and intrapulmonary veins in patients with anti-MDA5 antibody-positive DM-ILD.

CONCLUSION:

Serum IFNλ3 is a promising biomarker for identifying patients at high risk of poor outcomes in anti-MDA5 antibody-positive DM-ILD.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Autoantibodies / Lung Diseases, Interstitial / Dermatomyositis / Interferon-Induced Helicase, IFIH1 / Interferon Lambda Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Year: 2024 Type: Article

Full text: 1 Database: MEDLINE Main subject: Autoantibodies / Lung Diseases, Interstitial / Dermatomyositis / Interferon-Induced Helicase, IFIH1 / Interferon Lambda Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Year: 2024 Type: Article