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- Data for: Multidimensional analyses of proinsulin peptide-specific regulatory T cells induced by tolerogenic dendritic cellsCyTOF data: T cells stimulated with tolerogenic dendritic cells (TtolDC) or inflammatory dendritic cells (TmDC). Cells are labelled with 35 metal-tagged antibodies and acquired in CyTOF 2. Files are exported after gating for singlets and CD45+.
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- Data for: Changing epidemiology of immune-mediated inflammatory diseases in immigrants: a systematic review of population-based studiesPRISMA flow diagrams Tabulation of included studies Search strategies
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- Data for: Myeloid sphingosine-1-phosphate receptor 1 is important for CNS autoimmunity and neuroinflammationProcessed data for this manuscript.
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- Data for: T cells are influenced by a long non-coding RNA in the autoimmune associated PTPN2 locusRNA sequencing was performed for Jurkat cells following antisense LNA™ GapmeR/dsiRNA-mediated knockdown of LINC0882 using two time points – 24h and 48h (2 experiments each), by Illumina HiSeq 2500 sequencer.
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- Dataset related to article "Interleukin-6 receptor blocking with intravenous tocilizumab in COVID-19 severe acute respiratory distress syndrome: A retrospective case-control survival analysis of 128 patients"This record contains raw data related to article "Interleukin-6 receptor blocking with intravenous tocilizumab in COVID-19 severe acute respiratory distress syndrome: A retrospective case-control survival analysis of 128 patients" In cases of COVID-19 acute respiratory distress syndrome, an excessive host inflammatory response has been reported, with elevated serum interleukin-6 levels. In this multicenter retrospective cohort study we included adult patients with COVID-19, need of respiratory support, and elevated C-reactive protein who received intravenous tocilizumab in addition to standard of care. Control patients not receiving tocilizumab were matched for sex, age and respiratory support. We selected survival as the primary endpoint, along with need for invasive ventilation, thrombosis, hemorrhage, and infections as secondary endpoints at 30 days. We included 64 patients with COVID-19 in the tocilizumab group and 64 matched controls. At baseline the tocilizumab group had longer symptom duration (13 ± 5 vs. 9 ± 5 days) and received hydroxychloroquine more often than controls (100% vs. 81%). The mortality rate was similar between groups (27% with tocilizumab vs. 38%) and at multivariable analysis risk of death was not significantly influenced by tocilizumab (hazard ratio 0.61, 95% confidence interval 0.33-1.15), while being associated with the use at baseline of non invasive mechanical or invasive ventilation, and the presence of comorbidities. Among secondary outcomes, tocilizumab was associated with a lower probability of requiring invasive ventilation (hazard ratio 0.36, 95% confidence interval 0.16-0.83; P = 0.017) but not with the risk of thrombosis, bleeding, or infections. The use of intravenous tocilizumab was not associated with changes in 30-day mortality in patients with COVID-19 severe respiratory impairment. Among the secondary outcomes there was less use of invasive ventilation in the tocilizumab group
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- Discoidin domain of human CASPR2
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- Crystal structure of HLA-DRB1*04:01 with modified alpha-enolase peptide 326-340 (arginine 327 to citrulline)
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- Crystal structure of HLA-DRB1*04:01 with the alpha-enolase peptide 326-340
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