Autoantibodies against C5aR1, C3aR1, CXCR3, and CXCR4 are decreased in primary Sjogren's syndrome. (March 2021)
- Record Type:
- Journal Article
- Title:
- Autoantibodies against C5aR1, C3aR1, CXCR3, and CXCR4 are decreased in primary Sjogren's syndrome. (March 2021)
- Main Title:
- Autoantibodies against C5aR1, C3aR1, CXCR3, and CXCR4 are decreased in primary Sjogren's syndrome
- Authors:
- Yue, Xiaoyang
Deng, Fengyuan
Chen, Juan
Yin, Junping
Zheng, Junfeng
Chen, Yan
Huang, Qiaoniang
Gao, Xing
Liu, Zuguo
Luo, Jiao
Müller, Antje
Heidecke, Harald
Riemekasten, Gabriela
Petersen, Frank
Yu, Xinhua - Abstract:
- Highlights: Autoantibodies to C5aR1, C3aR1, CXCR3 and CXCR4 are decresed in pSS and RA. Autoantibodies to CXCR3 and CXCR4 correlate with circulating lymphocytes in pSS. Correlation signature of anti-GPCR antibodies is associateded to lung invovlement in pSS. Abstract: Background: Networks formed of numerous autoantibodies (aabs) directed against G-protein coupled receptors (GPCR) have been suggested to play important role in autoimmune disorders. In present study, we aimed to evaluate the association between anti-GPCR antibodies and primary Sjogren's syndrome (pSS) to determine the potential pathogenic factors. Methods: By applying a cell membrane-based ELISA technique, which is capable of detecting aabs against conformational epitopes within GPCR, serum levels of fourteen GPCR were determined in well-characterized patients with pSS (n = 52) and gender-matched healthy controls (n = 54). Comparisons between groups were analyzed by two-tailed Mann-Whitney U test, Bonferroni correction was applied for multiple comparisons. Spearman`s rank correlation coefficients were calculated between variables and visualized by heat map. Results: Compared to healthy subjects, sera of patients with pSS showed significantly higher binding to β2AR and ETAR, but lower binding to C5aR1, C3aR1, CXCR3, and CXCR4. Autoantibodies against C5aR1, C3aR1, CXCR3, and CXCR4 were also decreased in patients with rheumatoid arthritis. In pSS patients, levels of anti-CXCR3 and anti-CXCR4 antibodies wereHighlights: Autoantibodies to C5aR1, C3aR1, CXCR3 and CXCR4 are decresed in pSS and RA. Autoantibodies to CXCR3 and CXCR4 correlate with circulating lymphocytes in pSS. Correlation signature of anti-GPCR antibodies is associateded to lung invovlement in pSS. Abstract: Background: Networks formed of numerous autoantibodies (aabs) directed against G-protein coupled receptors (GPCR) have been suggested to play important role in autoimmune disorders. In present study, we aimed to evaluate the association between anti-GPCR antibodies and primary Sjogren's syndrome (pSS) to determine the potential pathogenic factors. Methods: By applying a cell membrane-based ELISA technique, which is capable of detecting aabs against conformational epitopes within GPCR, serum levels of fourteen GPCR were determined in well-characterized patients with pSS (n = 52) and gender-matched healthy controls (n = 54). Comparisons between groups were analyzed by two-tailed Mann-Whitney U test, Bonferroni correction was applied for multiple comparisons. Spearman`s rank correlation coefficients were calculated between variables and visualized by heat map. Results: Compared to healthy subjects, sera of patients with pSS showed significantly higher binding to β2AR and ETAR, but lower binding to C5aR1, C3aR1, CXCR3, and CXCR4. Autoantibodies against C5aR1, C3aR1, CXCR3, and CXCR4 were also decreased in patients with rheumatoid arthritis. In pSS patients, levels of anti-CXCR3 and anti-CXCR4 antibodies were negatively correlated with circulating lymphocyte counts. Furthermore, correlation signatures of anti-GPCR antibodies changed dramatically in the patients with pulmonary involvement. Conclusions: This study demonstrates an association between pSS and autoantibodies recognizing GPCR, especially those functionally involved in immune cell migration and exocrine glandular secretion. … (more)
- Is Part Of:
- Molecular immunology. Volume 131(2021)
- Journal:
- Molecular immunology
- Issue:
- Volume 131(2021)
- Issue Display:
- Volume 131, Issue 2021 (2021)
- Year:
- 2021
- Volume:
- 131
- Issue:
- 2021
- Issue Sort Value:
- 2021-0131-2021-0000
- Page Start:
- 112
- Page End:
- 120
- Publication Date:
- 2021-03
- Subjects:
- AT1R angiotensin II receptor type 1 -- aabs Autoantibodies -- CXCR3 C-X-C motif chemokine receptor 3 -- CXCR4 C-X-C motif chemokine receptor 4 -- C3aR1 complement component 3a receptor 1 -- C5aR1 complement component 5a receptor 1 -- ETAR endothelin-1 type A receptor -- ESSDAI EULAR Sjögren's syndrome disease activity index -- GPCR G-protein coupled receptors -- HD Healthy donors -- M3R muscarinic M3 receptors -- pSS Primary Sjogren's syndrome -- PAR1 proteinase activation receptor 1 -- PAR2 proteinase activation receptor 2 -- VEGFR1 vascular endothelial growth factor receptor 1 -- VEGFR2 vascular endothelial growth factor receptor 2 -- β1AR β1 adrenergic receptor -- β2AR β2 adrenergic receptor
Autoantibodies to G-protein coupled receptors -- Primary Sjogren's syndrome -- Complement receptors -- Chemokines receptors -- β2 adrenergic receptor -- Rheumatoid arthritis.
Immunochemistry -- Periodicals
Molecular biology -- Periodicals
Immunochemistry -- Periodicals
Allergy and Immunology -- Periodicals
Molecular Biology -- Periodicals
Immunochimie -- Périodiques
Biologie moléculaire -- Périodiques
Immunochemistry
Molecular biology
Periodicals
Electronic journals
571.96 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01615890 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.molimm.2020.12.027 ↗
- Languages:
- English
- ISSNs:
- 0161-5890
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