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Title: Anti-aminoacyl tRNA synthetase antibodies showing the discrepancy between enzyme-linked immunosorbent assay and RNA-immunoprecipitation
Authors: Sasai, Tsuneo
Ishikawa, Yuki
Nakashima, Ran
Isayama, Takuya
Tanizawa, Kiminobu
Handa, Tomohiro
Shirakashi, Mirei  kyouindb  KAKEN_id  orcid https://orcid.org/0000-0003-1135-0463 (unconfirmed)
Hiwa, Ryosuke  kyouindb  KAKEN_id  orcid https://orcid.org/0000-0001-6968-5712 (unconfirmed)
Tsuji, Hideaki  kyouindb  KAKEN_id  orcid https://orcid.org/0000-0002-2521-246X (unconfirmed)
Kitagori, Koji  kyouindb  KAKEN_id  orcid https://orcid.org/0000-0001-8056-8648 (unconfirmed)
Akizuki, Shuji  kyouindb  KAKEN_id
Yoshifuji, Hajime  kyouindb  KAKEN_id  orcid https://orcid.org/0000-0001-7082-4900 (unconfirmed)
Mimori, Tsuneyo
Morinobu, Akio  kyouindb  KAKEN_id  orcid https://orcid.org/0000-0002-4672-638X (unconfirmed)
Author's alias: 笹井, 蘭
Keywords: Anti-aminoacyl tRNA synthetase antibody
anti-synthetase syndrome
dermatomyositis
interstitial lung disease
Issue Date: 2024
Publisher: Taylor & Francis
The Japanese Society of Clinical Immunology
Journal title: Immunological Medicine
Volume: 47
Issue: 3
Start page: 166
End page: 175
Abstract: Anti-aminoacyl-tRNA synthetase (ARS) antibodies are myositis-specific antibodies associated with anti-synthetase syndrome (ASSD). Some patients are positive for anti-ARS antibodies on enzyme-linked immunosorbent assay (ELISA) but negative on RNA-immunoprecipitation (RNA-IP) (the gold standard method). Whether these patients should be considered truly positive for anti-ARS antibodies remains unclear. Therefore, we investigated the clinical characteristics of these patients and verified the authenticity of their anti-ARS positivity. Patients who were positive for anti-ARS antibodies on ELISA were divided into the non-discrepant (positive on RNA-IP, n = 52) and discrepant (negative on RNA-IP, n = 8) groups. Patient clinical characteristics were compared between the groups. For each positive individual, the authenticity of anti-ARS antibody positivity on ELISA was cross-examined using protein-IP and western blotting. All patients in the discrepant group had lung involvement, including five (63%) with interstitial lung disease. The overall survival time was significantly lower in the discrepant group than in the non-discrepant group (p < 0.05). Validation tests confirmed the presence of anti-ARS antibodies in the sera of the discrepant group but indicated different reactivity from typical anti-ARS antibodies. In conclusion, some anti-ARS antibodies are detected by ELISA but not RNA-IP. Such anti-ARS antibody discrepancies need further elucidation to attain validation of the diagnostic process in ASSD.
Rights: © 2024 The author(s). Published by Informa uK limited, trading as Taylor & Francis group on behalf of the Japanese Society of clinical Immunology.
This is an open access article distributed under the terms of the creative commons attribution license , which permits unre-stricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
URI: http://hdl.handle.net/2433/292484
DOI(Published Version): 10.1080/25785826.2024.2328918
PubMed ID: 38488763
Appears in Collections:Journal Articles

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