TNF, tumor necrosis factor, 7124

N. diseases: 2724; N. variants: 31
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.100 Biomarker disease BEFREE The purpose of the present study was to describe our experience with the recombinant Fab' antibody fragment against TNF-α Certolizumab Pegol (CZP) in patients with Behçet's disease (BD) refractory to standardized therapies and previous biologic agents. 28712320 2017
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.100 Biomarker disease BEFREE No differences existed in patients switched from other tumor necrosis factor (TNF)-α inhibitors about efficacy at 12 weeks (p = 0.13) and rapidity of response (p = 0.93) while relapses (p = 0.01) and ADA discontinuation at 24 months (p = 0.001) were significantly more common.Adverse events occurred in 10 patients.ADA confirmed its effectiveness in BD. 27679471 2017
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.100 Biomarker disease BEFREE The activating transcription factor 3 (ATF3) transcript level was increased in PBMCs from patients with stable BD compared to that in PBMCs from HCs. siRNAs targeting C/EBPβ and C/EBPδ significantly reduced the production of IL-6 and TNF-α in lipopolysaccharide-stimulated CD11b+ cells from patients with BD as well as from HCs. 28392644 2017
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.100 GeneticVariation disease BEFREE To investigate whether single nucleotide polymorphisms (SNPs) of the Tumor Necrosis Factor Superfamily 4 (TNFSF4) gene are associated with Vogt-Koyanagi-Harada (VKH) and Behcet's disease (BD) in a Chinese Han population. 27872495 2016
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.100 GeneticVariation disease BEFREE Nine BD patients (mean age 34.55 ± 16.30 years) refractory to tumor necrosis factor blockers and standardized therapies are reported in our survey. 24305945 2015
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.100 Biomarker disease BEFREE Interleukin-23 Receptor Gene Polymorphism May Enhance Expression of the IL-23 Receptor, IL-17, TNF-α and IL-6 in Behcet's Disease. 26222305 2015
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.100 GeneticVariation disease BEFREE The present study might suggest that TNF-α -308A/G, IL-10 -1082G/A, -819C/T, -592C/A polymorphisms are associated with BD susceptibility. 24267724 2013
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.100 GeneticVariation disease BEFREE Similarly, the meta-analysis showed a significant association of the TNF -857T/C polymorphism with BD (OR = 0.758, 95% CI = 0.593-0.968, p = 0.027). 24049437 2013
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.100 Biomarker disease BEFREE We report the first association between BD and TNF-α SNPs in Moroccan patients. 22711844 2012
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.100 Biomarker disease BEFREE We assayed aqueous humor (AH) samples from patients with Behçet's disease (BD), Vogt-Koyanagi-Harada (VKH) disease, and HLA-B27-associated uveitis and control patients for the proinflammatory cytokines IL-15, IL-17, interferon-γ and tumor necrosis factor-α and the immunosuppressive cytokine IL-10. 21334264 2011
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.100 GeneticVariation disease BEFREE Data suggest that other HLA (HLA-C, HLA-DR) and HLA-related [MHC Class I chain-related gene A (MIC-A), TNF-α] genes may play a role in BD co-susceptibility or pathogenesis. 21059670 2011
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.100 Biomarker disease BEFREE No apparent differences in interleukin (IL)-4, 6, 8 and 10 were observed, whereas production of soluble IL-2-receptor and tumor necrosis factor (TNF)-alpha were more pronounced in the BD group. 21816027 2011
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.100 GeneticVariation disease BEFREE Our study indicates that functional TNF-α, IL10 genotypes or combined TNF-α, IL10 genotypes do not play a role in BS susceptibility in Turkish BS patients. 20191386 2010
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.100 GeneticVariation disease BEFREE Particular genotypes and haplotypes in TNF-α were over-represented in BD, which may, in turn, predispose individuals to this disease. 21059493 2010
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.100 GeneticVariation disease BEFREE A literature review was performed using MEDLINE, EMBASE and the Cochrane Central Register of Controlled Trials for original studies published in English up to October 31, 2009 and that examined the association of the TNF-alpha promoter polymorphisms with Behçet's disease. 20470944 2010
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.100 AlteredExpression disease BEFREE Since NRAMP1 plays a role in the up-regulation of the TNF-alpha, iNOS and MHC expression, it may also be a candidate gene for Behçet's syndrome (BS). 18998137 2009
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.100 GeneticVariation disease BEFREE The single nucleotide polymorphisms of the IL-6 and IL-8 receptor genes and the TNF-alpha gene analysed here do not appear to be associated with Behçet's disease. 19026125 2009
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.100 Biomarker disease BEFREE These results suggest that TNF-alpha is a susceptibility gene for BD in patients from Iranian Azeri Turk ethnic group. 19774383 2009
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.100 GeneticVariation disease BEFREE We also sought to determine the effects of periodontal condition and TNF-alpha-1031T/C polymorphism on clinical severity of BD. 18355201 2008
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.100 Biomarker disease BEFREE Therefore, the TNF molecule may have an important genetically and/or functionally implication in the pathogenesis of BD in the Tunisian population. 17349875 2007
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.100 Biomarker disease LHGDN The aim of the study is to compare stimulated production of TNF-alpha by PBM of BD patients with that of healthy volunteers (HV) and to examine correlations between the ability of PBM to produce TNF-alpha and organ/system involvement in patients with BD. 16897113 2007
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.100 GeneticVariation disease BEFREE Patients with the novel -646A allele of the TNFalpha promoter region were significantly associated with the expression of the HLA-B51 allele (p(corr) = 0.006), although this novel polymorphic allele was not associated with BD susceptibility. 17657677 2007
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.100 GeneticVariation disease LHGDN Six polymorphisms in the promoter region of TNFA were genotyped in 254 BD patients and 344 control subjects, via the PCR-RFLP technique. 16891799 2006
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.100 GeneticVariation disease BEFREE Association of TNFA promoter region haplotype in Behçet's Disease. 16891799 2006
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.100 GeneticVariation disease BEFREE To investigate the possible relation of the TNF-alpha-1031 T/C polymorphism with susceptibility to BD in a Turkish population and to determine the functional importance of this polymorphism. 16882174 2006