Molecular Remission at T cell level in Patients with Rheumatoid Arthritis
Autor: | Tsutomu Takeuchi, Keiko Koga, Jun Inamo, Yuumi Okuzono, Masaru Takeshita, Yasushi Kondo, Katsuya Suzuki, Rina Kurisu, Maiko Takiguchi, Akihiko Yoshimura, Yoshiaki Kassai |
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Rok vydání: | 2021 |
Předmět: |
Oncology
CD4-Positive T-Lymphocytes medicine.medical_specialty T cell Science Predictive medicine CD8-Positive T-Lymphocytes Article Pathogenesis Arthritis Rheumatoid Machine Learning chemistry.chemical_compound Text mining Tocilizumab Internal medicine medicine Humans In patient Rheumatoid arthritis Transcriptomics Multidisciplinary business.industry Remission Induction medicine.disease Gene expression profiling medicine.anatomical_structure Cross-Sectional Studies chemistry Medicine business Transcriptome CD8 |
Zdroj: | Scientific Reports Scientific Reports, Vol 11, Iss 1, Pp 1-9 (2021) |
DOI: | 10.21203/rs.3.rs-51665/v3 |
Popis: | Introduction. While numerous disease-modifying anti-rheumatic drugs (DMARDs) have brought about a dramatic paradigm shift in the management of rheumatoid arthritis (RA), unmet needs remain, such as the small proportion of patients who achieve drug-free status. The aim of this study was to explore key molecules for remission at the T cell level, which are known to be deeply involved in RA pathogenesis, and investigate the disease course of patients who achieved molecular remission (MR). Methods. We enrolled a total of 46 patients with RA and 10 healthy controls (HCs). We performed gene expression profiling and selected remission signature genes in CD4+ T cells and CD8+ T cells from patients with RA using machine learning methods. In addition, we investigated the benefits of achieving MR on disease control. Results. We identified 9 and 23 genes that were associated with clinical remission in CD4+ and CD8+ T cells, respectively. Principal component analysis (PCA) demonstrated that their expression profiling was similar to those in HCs. For the remission signature genes in CD4+ T cells, the PCA result was reproduced using a validation cohort, indicating the robustness of these genes. A trend toward better disease control was observed during 12 months of follow-up in patients treated with tocilizumab in deep MR compared with those in non-deep MR, although the difference was not significant. Conclusion. We identified robust genes that represent remission status in CD4+ T cells using machine learning techniques. The current study will promote our understanding of the molecular mechanisms necessary to achieve deep remission during the management of RA. Trial registration: Not required. |
Databáze: | OpenAIRE |
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