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Disease-specific autoantibody production in the lungs and salivary glands of anti-synthetase syndrome.
Takeshita, Masaru; Suzuki, Katsuya; Nakazawa, Maho; Kamata, Hirofumi; Ishii, Makoto; Oyamada, Yoshitaka; Oshima, Hisaji; Usuda, Satoshi; Tsunoda, Kazuyuki; Takeuchi, Tsutomu.
Affiliation
  • Takeshita M; Division of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Shinjuku, Japan.
  • Suzuki K; Division of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Shinjuku, Japan.
  • Nakazawa M; Division of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Shinjuku, Japan.
  • Kamata H; Division of Rheumatology, Department of Medicine, Solna, Karolinska Institutet, Stockholm, Sweden.
  • Ishii M; Division of Pulmonary Medicine, Department of Internal Medicine, Keio University School of Medicine, Shinjuku, Japan.
  • Oyamada Y; Division of Pulmonary Medicine, Department of Internal Medicine, Keio University School of Medicine, Shinjuku, Japan.
  • Oshima H; Division of Respiratory Medicine, Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Usuda S; Department of Respiratory Medicine, National Tokyo Medical Center, Meguro, Japan.
  • Tsunoda K; Department of Connective Tissue Diseases, National Tokyo Medical Center, Meguro, Japan.
  • Takeuchi T; Department of Dentistry and Oral Surgery, Keio University School of Medicine, Shinjuku, Japan.
Front Immunol ; 15: 1265792, 2024.
Article in En | MEDLINE | ID: mdl-38938569
ABSTRACT
Interstitial lung disease is a common complication of anti-synthetase syndrome (ASS), and lymphocytic infiltration is often observed in the lesion. We have recently reported that disease-specific autoantibodies are produced by infiltrating lymphocytes in some autoimmune diseases. Here, we investigate the antigen specificity of B cells in the lung lesions of ASS patients. A total of 177 antibodies were produced from antibody-secreting cells in bronchoalveolar fluid (BALF) of three each of serum anti-Jo-1 and serum anti-EJ antibody-positive patients. Twelve to 30% and 50 to 62% of these antibodies were disease-specific autoantibodies, respectively. These autoantibodies recognized conformational epitopes of the whole self-antigen and had affinity maturations, indicating that self-antigens themselves are the target of humoral immunity. In addition, 100 antibodies were produced from two salivary gland tissues, obtained by chance, of ASS patients. Salivary glands are not generally recognized as lesions of ASS, but unexpectedly, ASS-related autoantibody production was also observed similar to that of BALF. Immunostaining confirmed the presence of ASS-related autoantibody-producing cells in salivary glands. Our results suggest that disease-specific autoantibody production at lesion sites is a common pathogenesis of autoimmune diseases, and that tissue-specific production of autoantibodies can provide insights regarding the distribution of organ manifestations in autoimmune diseases.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Salivary Glands / Autoantibodies / Lung / Myositis Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Front Immunol Year: 2024 Document type: Article Affiliation country: Japan Country of publication: Switzerland

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Salivary Glands / Autoantibodies / Lung / Myositis Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Front Immunol Year: 2024 Document type: Article Affiliation country: Japan Country of publication: Switzerland