TNFRSF14, TNF receptor superfamily member 14, 8764

N. diseases: 100; N. variants: 3
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.100 GeneticVariation disease GWASCAT Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. 26974007 2016
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.100 GeneticVariation disease GWASCAT Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. 26974007 2016
CUI: C0019340
Disease: Herpes NOS
Herpes NOS
0.090 Biomarker disease BEFREE TNFRSF14 is known as herpes virus entry mediator (HVEM), and herpes viruses have been involved in the aetiology of multiple sclerosis (MS). 20962851 2011
CUI: C0019340
Disease: Herpes NOS
Herpes NOS
0.090 Biomarker disease BEFREE Herpes virus entry mediator (HVEM) is a member of the tumor necrosis factor (TNF) receptor superfamily (TNFRSF14), which serves as a receptor for herpes viruses and cytokines such as lymphotoxin-alpha (LT-alpha) and LIGHT (lymphotoxin-like inducible protein that competes with glycoprotein D for herpes virus entry on T cells). 19680232 2010
CUI: C0019340
Disease: Herpes NOS
Herpes NOS
0.090 AlteredExpression disease BEFREE To determine cellular and temporal expression patterns of herpes virus entry mediator (HVEM, Tnfrsf14) in the murine cornea during the course of herpes simplex virus 1 (HSV-1) infection, the impact of this expression on pathogenesis, and whether alterations in HVEM or downstream HVEM-mediated effects ameliorate corneal disease. 28114589 2017
CUI: C0019340
Disease: Herpes NOS
Herpes NOS
0.090 Biomarker disease BEFREE Overexpression of LIGHT (LIGHT: homologous to lymphotoxins, indicating inducible expression, and competes with herpes simplex virus glycoprotein D for herpes virus entry mediator [HVEM/TR2]) in MDA-MB-231 human breast cancer cells was observed to suppress tumor growth in vivo. 12651068 2003
CUI: C0019340
Disease: Herpes NOS
Herpes NOS
0.090 Biomarker disease BEFREE The co-signaling molecule, LIGHT, is particularly well suited for use in vaccine development as it delivers a potent co-stimulatory signal through the Herpes virus entry mediator (HVEM) receptor on T cells and facilitates tumor-specific T cell immunity. 21877247 2012
CUI: C0019340
Disease: Herpes NOS
Herpes NOS
0.090 Biomarker disease BEFREE Characterization of Sex Differences in Ocular Herpes Simplex Virus 1 Infection and Herpes Stromal Keratitis Pathogenesis of Wild-Type and Herpesvirus Entry Mediator Knockout Mice. 30918059 2019
CUI: C0019340
Disease: Herpes NOS
Herpes NOS
0.090 Biomarker disease BEFREE One such gene, tumor necrosis factor receptor superfamily 14 (TNFRSF14), abnormal in 40% of FL patients, encodes the herpes virus entry mediator (HVEM) which limits T-cell activation via ligation of the B- and T-lymphocyte attenuator. 27103745 2016
CUI: C0019340
Disease: Herpes NOS
Herpes NOS
0.090 Biomarker disease BEFREE We observed spontaneous osteoclastogenesis with a significant increase in OC formation and bone resorbing activity in late-stage CKD and HD patients when compared with early-stage CKD patients and healthy donors, likely due to an increased expression of RANKL and LIGHT (homologous to Lymphotoxins exhibiting Inducible expression and competing with herpes simplex virus Glycoprotein D for herpes virus entry mediator [HVEM], a receptor expressed by T lymphocytes) in PBMCs. 28992140 2018
CUI: C0019340
Disease: Herpes NOS
Herpes NOS
0.090 Biomarker disease BEFREE Using respiratory virus infection, we show that herpes virus entry mediator (HVEM; TNFRSF14), a member of the TNF receptor superfamily, provides key signals for MPEC persistence. 28864473 2017
Secondary malignant neoplasm of lymph node
0.040 AlteredExpression disease BEFREE Similarly, the high expression of HVEM was also significantly correlated with lymph node metastasis (<i>P</i>=0.007) and depth of invasion (<i>P</i>=0.011). 28243127 2017
Secondary malignant neoplasm of lymph node
0.040 AlteredExpression disease BEFREE HVEM expression was found to be significantly correlated with depth of tumor invasion and lymph node metastasis. 24249528 2014
Secondary malignant neoplasm of lymph node
0.040 AlteredExpression disease BEFREE HVEM is highly expressed in ovarian serous adenocarcinoma tissues and correlated with the patient clinicopathological features, such as TNM staging, lymph node metastasis and recurrence. 28365939 2017
Secondary malignant neoplasm of lymph node
0.040 GeneticVariation disease BEFREE Our research also indicated an association between polymorphisms of HVEM and clinicopathologic features, including lymph node metastasis, estrogen receptor, progesterone receptor and P53. 23976978 2013
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma
0.030 Biomarker disease BEFREE The cytokine TNFSF14 [homologous to Lymphotoxin, exhibits Inducible expression and competes with HSV Glycoprotein D for binding to HVEM, a receptor expressed on T lymphocytes (LIGHT)] has been shown in mouse models to be important for development of lung tissue remodeling that is characteristic of asthma, idiopathic pulmonary fibrosis (IPF), and systemic sclerosis (SSc). 29616048 2018
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma
0.030 Biomarker disease BEFREE Here, we show that the tumor necrosis factor (TNF) superfamily protein LIGHT (homologous to lymphotoxin, exhibits inducible expression, and competes with HSV glycoprotein D for binding to HVEM, a receptor expressed on T lymphocytes) is required for experimental atopic dermatitis, and LIGHT directly controls keratinocyte hyperplasia, and production of periostin, a matricellular protein that contributes to the clinical features of atopic dermatitis as well as other skin diseases such as scleroderma. 29339444 2018
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma
0.030 Biomarker disease BEFREE Increased expression of the TNF superfamily member LIGHT/TNFSF14 and its receptors (HVEM and LTßR) in patients with systemic sclerosis. 30508197 2019
CUI: C0598766
Disease: Leukemogenesis
Leukemogenesis
0.030 Biomarker disease BEFREE These data suggest that HVEM interaction with BTLA may play a role in lymphomagenesis by interfering with Vγ9Vδ2 T-cell proliferation. 23692853 2013
CUI: C0598766
Disease: Leukemogenesis
Leukemogenesis
0.030 Biomarker disease BEFREE Mutation-associated loss of this interaction promotes B cell proliferation through exaggerated T cell help, explaining how HVEM loss contributes to GC lymphomagenesis and revealing a cell-extrinsic tumor-suppressor role for BTLA. 31433965 2019
CUI: C0598766
Disease: Leukemogenesis
Leukemogenesis
0.030 Biomarker disease BEFREE These results establish that HVEM restrains the T helper signals delivered to B cells to influence GC selection outcomes, and they suggest that BTLA functions as a cell-extrinsic suppressor of GC B cell lymphomagenesis. 31204070 2019
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.030 AlteredExpression disease BEFREE Clinical impact of herpesvirus entry mediator expression in human hepatocellular carcinoma. 25468715 2015
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.030 Biomarker disease BEFREE In the discovery cohort (n = 94), we found that lack of, or low, tumor expression of PD-L1 (<i>p</i> < 0.001), Galectin-9 (<i>p</i> < 0.001) and HVEM (<i>p</i> < 0.001), and low CD8<sup>+</sup>TIL count (<i>p</i> = 0.016), were associated with poor HCC-specific survival. 28344887 2017
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.030 Biomarker disease BEFREE Collectively, our data suggested that the BTLA/HVEM pathway contributes to peripheral T cell suppression in HCC patients, and BTLA/HVEM may serve as attractive targets for HCC immunotherapy. 30116751 2018
CUI: C0003864
Disease: Arthritis
Arthritis
0.020 Biomarker disease BEFREE In conclusion, HVEM-Ig aggravates autoimmunity in collagen-induced arthritis, which is possibly mediated by interaction with B and T lymphocyte attenuator (BTLA) or CD160, despite the blockade of LIGHT. 19234211 2009