Clinical correlates of a subset of anti-fibroblast antibodies in systemic sclerosis
Clinical Immunology, ISSN: 1521-6616, Vol: 255, Page: 109740
2023
- 1Citations
- 7Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations1
- Citation Indexes1
- CrossRef1
- Captures7
- Readers7
Article Description
Anti-fibroblast antibodies (AFA) have been reported in systemic sclerosis (SSc) and are known to promote fibroblast activation. Aim of this study was to characterize the fine specificity of AFA and to analyze any correlations with clinical parameters associated to fibrosis. To this end, AFA were affinity-purified from a patient with diffuse cutaneous SSc (dcSSc) and interstitial lung disease (ILD). Panning of a phage display peptide library with purified AFA identified the motif . The peptide p121, bearing the AFA-specific motif, was used in ELISA to screen sera from 186 SSc patients and 81 healthy donors. Anti-p121 Ab serum levels were statistically higher in SSc than in healthy groups, and directly associated with dcSSc, reduced FVC (FVC < 70), and ILD. Given these clinical correlates, this study lays the groundwork for the identification of the antigen recognized by anti-p121 Ab, which might represent a novel therapeutic target for ILD.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S152166162300503X; http://dx.doi.org/10.1016/j.clim.2023.109740; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85168938484&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/37586673; https://linkinghub.elsevier.com/retrieve/pii/S152166162300503X; https://dx.doi.org/10.1016/j.clim.2023.109740
Elsevier BV
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