AB0173 LONG NON-CODING RNA, LINC00487 EXPRESSION IS UPREGULATED IN B CELLS AND CORRELATES TO DISEASE ACTIVITY IN PATIENTS WITH PRIMARY SJöGREN'S SYNDROME. (June 2019)

• Record Type: Journal Article
• Authors: Inamo, Jun; Suzuki, Katsuya; Takeshita, Masaru; Kasai, Yoshiaki; Kurisu, Rina; Takiguchi, Maiko; Okuzono, Yuumi; Tasaki, Shinya; Takeuchi, Tsutomu
• Is Part Of: Annals of the rheumatic diseases. Volume 78(2019)Supplement 2
• Page Start: 1545
• Page End: 1545
• Publication Date: 2019-06
• Subjects: Rheumatism -- Periodicals; 616.723005
• DOI: 10.1136/annrheumdis-2019-eular.3939
• Languages: English
• ISSNs: 0003-4967

Abstract

Abstract : Background: Primary Sjögren's syndrome (pSS) is a systemic autoimmune disease characterized by interferon signature [1] and exocrine gland dysfunction which leads to dryness of the eyes and mouth [2]. B cells are considered to play an important role in the pathogenesis of pSS. Dysregulation of B cells can lead to production of anti-Sjögren's syndrome-related antigen A (anti-SSA) autoantibodies. Objectives: We investigated the differential gene expression of peripheral B cell subsets to reveal the precise role of B cells in the pathogenesis of pSS. Methods: We enrolled pSS patients (n=6) and healthy controls (HC) (n=6), with matching for age and sex. Peripheral B cells acquired from the participants were separated by cell sorting into 4 subsets: CD38 - IgD +, CD38 + IgD +, CD38 high IgD + and CD38 ± IgD - . Total RNA was extracted and gene expression was measured using the Human Genome U133 Plus 2.0 Array (Affymetrix). The data were bioinformatically analyzed with reference to the corresponding clinical information. Results: Using principal component and clustering analyses, we found that transcript expression patterns depended on cell type rather than clinical condition (pSS or HC). Interferon signaling was the most upregulated pathway in many of B cell subsets of pSS patients. As well as HLA and interferon signature genes, LINC00487 was upregulated significantly in all B cell subsets. Its fold changes in CD38 - IgD +, CD38 + IgD +, CD38 high IgD + and CD38 ± IgD - were 8.4 (p=0.038), 11.3 (p=0.014), 8.5 (p=0.089) and 6.37 (p=0.078), respectively. In addition, the normalized intensity value of LINC00487 was significantly correlated with disease activity score in all pSS B cell subsets, namely CD38 - IgD + (Figure A, r=0.96, p=0.002), CD38 + IgD + (Figure B, r=0.90, p=0.015), CD38 high IgD + (Figure C, r=0.81, p=0.049) and CD38 ± IgD - (Figure D, r=0.96, p=0.003). The expression of LINC00487 in B cell lines was regulated by IFNα. Conclusion: Compared to HC, patients with pSS showed upregulation of the interferon signaling pathway and LINC00487 gene in all B cell subsets. This upregulation correlated with disease activity and regulated by IFNα in B cell lines. These results may suggest that long non-coding RNA contributes to B cell dysregulation in patients with pSS and the precise role of LINC00487 in B cell and pathogenesis of pSS requires further study. References: [1] Muskardin TLW, et al. Nat Rev Rheumatol2018;14:214-228. [2] Qin, B. et al. Ann Rheum Dis. 2015;74:1983-1989. ESSDAI; EULAR Sjögren's Syndrome Disease Activity Index Disclosure of Interests: Jun Inamo: None declared, Katsuya Suzuki: None declared, Masaru Takeshita Grant/research support from: Novartis, Yoshiaki Kasai Employee of: Takeda Pharmaceutical Company Limited, Rina Kurisu Employee of: Takeda Pharmaceutical Company Limited, Maiko Takiguchi Employee of: Takeda Pharmaceutical Company Limited, Yuumi Okuzono Employee of: Takeda Pharmaceutical Company Limited, Shinya Tasaki Employee of: Takeda Pharmaceutical Company Limited, Tsutomu Takeuchi Grant/research support from: Astellas Pharma Inc, Chugai Pharmaceutical Co, Ltd., Daiichi Sankyo Co., Ltd., Takeda Pharmaceutical Co., Ltd., AbbVie GK, Asahikasei Pharma Corp., Mitsubishi Tanabe Pharma Co., Pfizer Japan Inc., Eisai Co., Ltd., AYUMI Pharmaceutical Corporation, Nipponkayaku Co. Ltd., Novartis Pharma K.K., Grant/research support from: AbbVie, Asahi Kasei, Astellas, AstraZeneca, AYUMI, Bristol-Myers Squibb, Chugai, Daiichi Sankyo, Eisai, Eli Lilly Japan, Janssen, Mitsubishi Tanabe, Nippon Kayaku, Novartis, Pfizer Japan Inc, Taiho, Taisho Toyama, Takeda, Teijin, Grant/research support from: Astellas Pharma Inc., Bristol Myers Squibb, Chugai Pharmaceutical Co., Ltd., Mitsubishi Tanabe Pharma Co., Pfizer Japan Inc., Santen Pharmaceutical Co., Ltd., Takeda Pharmaceutical Co., Ltd., Teijin Pharma Ltd., AbbVie GK, Asahi Kasei Pharma Corp., Taisho Toyama Pharmaceutical Co., Ltd., SymBio Pharmaceuticals Ltd., Janssen Pharmaceutical K.K., Celltrion Inc., Nipponkayaku Co. Ltd., and UCB Japan, Consultant for: Astra Zeneca K.K., Eli Lilly Japan K.K., Novartis Pharma K.K., Mitsubishi Tanabe Pharma Co., Abbivie GK, Nipponkayaku Co.Ltd, Janssen Pharmaceutical K.K., Astellas Pharma Inc., Taiho Pharmaceutical Co. Ltd., Chugai Pharmaceutical Co. Ltd., Taisho Toyama Pharmaceutical Co. Ltd., GlaxoSmithKline K.K., UCB Japan Co. Ltd., Consultant for: AbbVie, Asahi Kasei, Astellas, AstraZeneca, AYUMI, Bristol-Myers Squibb, Chugai, Daiichi Sankyo, Eisai, Eli Lilly Japan, Janssen, Mitsubishi Tanabe, Nippon Kayaku, Novartis, Pfizer Japan Inc, Taiho, Taisho Toyama, Takeda, Teijin, Consultant for: Astra Zeneca K.K., Eli Lilly Japan K.K., Novartis Pharma K.K., Mitsubishi Tanabe Pharma Co., Asahi Kasei Medical K.K., AbbVie GK, Daiichi Sankyo Co., Ltd., Bristol Myers Squibb, and Nipponkayaku Co. Ltd., Speakers bureau: Astellas Pharma Inc., Bristol Myers Squibb, Chugai Pharmaceutical Co., Ltd., Mitsubishi Tanabe Pharma Co., Pfizer Japan Inc., Santen Pharmaceutical Co., Ltd., Takeda Pharmaceutical Co., Ltd., Teijin Pharma Ltd., AbbVie GK, Asahi Kasei Pharma Corp., Taisho Toyama Pharmaceutical Co., Ltd., SymBio Pharmaceuticals Ltd., Janssen Pharmaceutical K.K., Celltrion Inc., Nipponkayaku Co. Ltd., and UCB Japan, Speakers bureau: AbbVie, Asahi Kasei, Astellas, AstraZeneca, AYUMI, Bristol-Myers Squibb, Chugai, Daiichi Sankyo, Eisai, Eli Lilly Japan, Janssen, Mitsubishi Tanabe, Nippon Kayaku, Novartis, Pfizer Japan Inc, Taiho, Taisho Toyama, Takeda, Teijin, Speakers bureau: AbbVie GK., Bristol–Myers K.K., Chugai Pharmaceutical Co. Ltd., Mitsubishi Tanabe Pharma Co., Pfizer Japan Inc., Astellas Pharma Inc, Diaichi Sankyo Co. Ltd., Eisai Co. Ltd., Sanofi K.K., Teijin Pharma Ltd., Takeda Pharmaceutical Co. Ltd., Novartis Pharma K.K.