Anti-interferon gamma-inducible protein 16 antibodies: Identification of a novel autoantigen in idiopathic interstitial pneumonia and its clinical characteristics based on a multicenter cohort study

Autoantibodies are detected in idiopathic interstitial pneumonias (IIPs) without a clear connective tissue disease diagnosis, and their clinical significance is unclear. This study aimed to identify a novel autoantibody in IIPs. We screened 295 IIP patients using a <sup>35</sup>S-methionine labeled protein immunoprecipitation assay. Candidate autoantigens were identified via protein array and confirmed by immunoprecipitation. Six sera from 295 IIP patients immunoprecipitated common tetrameric proteins (100 kDa). The protein array identified interferon gamma-inducible protein 16 (IFI16) as the candidate autoantigen. Patients with anti-IFI16 antibodies received immunosuppressants less frequently. Five-year survival rates were 50 %, 69 %, and 63 % (P = 0.60), and acute exacerbation-free rates were 50 %, 96 %, and 84 % (P = 0.15) for patients with anti-IFI16, anti-aminoacyl tRNA antibodies, and others. Anti-IFI16 is a novel autoantibody in IIPs. Patients with this antibody often receive less immunosuppressive therapy and could have a poor prognosis. Further research is needed to refine patient stratification and management.

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Publication Details

Journal
Clinical Immunology
Published
2024-09-30
DOI
https://doi.org/10.1016/j.clim.2024.110372
Citations
2
Primary Topic
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
Type
article
Field-Weighted Citation Impact
0.84

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article

Anti-interferon gamma-inducible protein 16 antibodies: Identification of a novel autoantigen in idiopathic interstitial pneumonia and its clinical characteristics based on a multicenter cohort study

Yasuhiro Kondo, Tsuneyo Mimori, Hideaki Tsuji, Kenji Kabashima et al.
2 citations
Clinical Immunology
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
0.84
article

Anti-interferon gamma-inducible protein 16 antibodies: Identification of a novel autoantigen in idiopathic interstitial pneumonia and its clinical characteristics based on a multicenter cohort study

Yasuhiro Kondo, Tsuneyo Mimori, Hideaki Tsuji, Kenji Kabashima, Hiromi Tomioka, Keisuke Tomii, Shogo Matsuda, Yasuhiko Yamano, Toshiaki Kogame, Hajime Yoshifuji, Ryosuke Hiwa, Tomohiro Handa, Ryo Tachikawa, Ran Nakashima, Akio Morinobu, Takuya Kotani, Shuji Akizuki, Kiminobu Tanizawa, Mirei Shirakashi, Y. Nohda, Tsuneo Sasai
article en
2 citations

Abstract

Autoantibodies are detected in idiopathic interstitial pneumonias (IIPs) without a clear connective tissue disease diagnosis, and their clinical significance is unclear. This study aimed to identify a novel autoantibody in IIPs. We screened 295 IIP patients using a <sup>35</sup>S-methionine labeled protein immunoprecipitation assay. Candidate autoantigens were identified via protein array and confirmed by immunoprecipitation. Six sera from 295 IIP patients immunoprecipitated common tetrameric proteins (100 kDa). The protein array identified interferon gamma-inducible protein 16 (IFI16) as the candidate autoantigen. Patients with anti-IFI16 antibodies received immunosuppressants less frequently. Five-year survival rates were 50 %, 69 %, and 63 % (P = 0.60), and acute exacerbation-free rates were 50 %, 96 %, and 84 % (P = 0.15) for patients with anti-IFI16, anti-aminoacyl tRNA antibodies, and others. Anti-IFI16 is a novel autoantibody in IIPs. Patients with this antibody often receive less immunosuppressive therapy and could have a poor prognosis. Further research is needed to refine patient stratification and management.

Clinical ImmunologyVol. 268
Kyoto University (JP), Kyoto Medical Center (JP), Institute for Rheumatic Diseases (Japan) (JP), Kobe City Medical Center West Hospital (JP), Tosei General Hospital (JP), Kobe City Medical Center General Hospital (JP), Takeda (Japan) (JP), Osaka University of Pharmaceutical Sciences (JP)
Takeda Science Foundation
Good health and well-being
Openalex Percentile: Top 24%
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
0.84
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