Message Board

Respected readers, authors and reviewers, you can add comments to this page on any questions about the contribution, review,        editing and publication of this journal. We will give you an answer as soon as possible. Thank you for your support!

Name
E-mail
Phone
Title
Content
Verification Code

JIANG Hailong, WANG Ningyuan, LU Yiming. Research advance of selective inhibitor of tumornecrosis factor receptor[J]. Journal of Pharmaceutical Practice and Service, 2015, 33(5): 392-395. doi: 10.3969/j.issn.1006-0111.2015.05.003
Citation: JIANG Hailong, WANG Ningyuan, LU Yiming. Research advance of selective inhibitor of tumornecrosis factor receptor[J]. Journal of Pharmaceutical Practice and Service, 2015, 33(5): 392-395. doi: 10.3969/j.issn.1006-0111.2015.05.003

Research advance of selective inhibitor of tumornecrosis factor receptor

doi: 10.3969/j.issn.1006-0111.2015.05.003
  • Received Date: 2014-04-18
  • Rev Recd Date: 2014-11-03
  • TNF signaling pathway was a valuable target, and anti-TNF drugs were successfully used to treat autoimmune and inflammatory diseases.But this therapy abrogate some beneficial TNF signaling, leading to increased risk of infection and malignancy, and the onset of new auto-immune diseases. Inhibiting the soluble TNF/TNFR1 axis while saving the beneficial transmembrane TNF/TNFR2 signaling untouched was a new approach.Because it inhibited the pathological effects of TNF and reduced the side effects, and opened the way for the treatment of other diseases in which TNFR2 inhibition was detrimental.The significance of the selective inhibition of TNFR1-mediated signaling pathways for TNF-related diseases was discussed and the mechanism of TNF identification TNFR was clarified, which might provide new ideas for the design of new drugs.
  • [1] Apostolaki M, Armaka M, Victoratos P,et al.Cellular mechanisms of TNF function in models of inflammation and autoimmunity[J].Curr Dir Autoimmun, 2010,11(2):1-26.
    [2] Mukai Y,Nakamura T, Yoshikawa M,et al. Solution of the structure of the TNF-TNFR2 complex[J]. Sci Signal,2010,3 (148): 1-10.
    [3] Hehlgans T, Pfeffer K. The intriguing biology of the tumounecrosis factor/tumour necrosis factor receptor superfamily players,rules and the games[J].Immunology,2005,115(1):1-20.
    [4] Mcllwain DR,Lang PA,Maretzky T,et al.IRhom2 regulation of TACE controls TNF-mediated protection against listeria and responses to LPS[J].Science,2012,335(6065):229-232.
    [5] Chen X, Wu X, Zhou Q,et al.TNFR2 is critical for the stabilization of the CD4+Foxp3+ Regulatory T cell phenotype in the inflammatory environmentl[J]. J Immuno,2013, 190(3):1076-1084.
    [6] Faustman D, Davis M. TNF receptor 2 pathway: drug target for autoimmune diseases[J].Nat Rev Drug Discov, 2010, 9(6):482-493.
    [7] Magis C, van der Sloot AM, Serrano L,et al. An improved understanding of TNFL/TNFR interactions using structure-based classi cations[J].Trends Biochem Sci,2012,37(9):353-363.
    [8] Dixon,Hyrich KL, Watson KD,et al. Drug-specific risk of tuberculosis in patients with rheumatoid arthritis treated with anti-TNF therapy: results from the British Society for Rheumatology Biologics Register (BSRBR)[J]. Ann Rheum Dis,2010,69(3):522-528.
    [9] Takeuchi T, Tatsuki Y, NogamiY,et al. Post marketing surveillance of the safety profile of infliximab in 5 000 Japanese patients with rheumatoid arthritis[J].Ann Rheum Dis,2008, 67(2):189-194.
    [10] Tang W, Lu Y, Tian QY,et al. The growth factor progranulin binds to TNF receptors and is therapeutic against inflammatory arthritis in mice[J]. Science, 2011, 332(6028): 478-484.
    [11] Deng GM, Zheng LX,Lenardo M,et al. Amelioration of inflammatory arthritis by targeting the pre-ligand assembly domain of tumor necrosis factor receptors[J].Nat Med,2005,10(11):1066-1072.
    [12] Hwang JR, Huh JH, Lee Y,et al. Insulin-like growth factor-binding protein-5 (IGFBP-5) inhibits TNF-a-induced NF-κB activity by binding to TNFR1[J]. Biochem Biophys Res Commun, 2011,405(4): 545-551.
    [13] Mukai Y, Shibata H, Nakamura T,et al. Structure-function relationship of tumor necrosis factor (TNF) and its receptor interaction based on 3D structural analysis of a fully active TNFR1-selective TNF mutant[J].J Mol Biol, 2009, 385(4):1221-1229.
    [14] Takasaki W,KajinoY,KajinoK,et al.Structure-based design and characterization of exocyclic peptidomimetics that inhibit TNF-αbinding to its receptor[J]. Nat Biotechnol, 1997, 15:1266-1270.
    [15] Mukaro. Selective activation of tumour necrosis factor receptor-mediated intacellular signalling pathways[D].Adelaide: School of Paediatrics and Reproductive Health,2009.
    [16] Chidnos-Rojas CL,Steward MW,PartidosCD,et al.Apeptidomimetic antagonist of TNF-alpha-mediated cytotoxicity identified from a phage-displayed random peptide library[J]. J Immunol,1998,161(10):5621-5626.
    [17] 尹丙姣,黄丽霞,梁慧芳,等.TNFR1封闭肽-hIgGFc融合蛋白和TNFR1封闭肽对TNF-α介导的生物学效应的封闭作用[J].中国免疫学杂志,2008,24(9):776-780.
    [18] Liang H, Yin B, Zhang H,et al. Blockade of tumor necrosis factor (TNF) receptor type1-mediated TNF-α signaling protected wistarrats from diet-Induced obesity and insulin resistance[J]. Endocrinology, 2008, 149(6):2943-2951.
    [19] Roland E,Sabine M,Jens N,et al. A humanized tumor necrosis factor receptor 1 (TNFR1)-specific antagonistic antibody for selective inhibition of tumor necrosis factor (TNF)action[J].J Immunother,2008,31(3):225-234.
    [20] Carter PH, Scherle PA, Muckelbauer JK,et al. Photochemically enhanced binding of small molecules to the tumor necrosis factor receptor-1 inhibits the binding of TNF-a[J]. PNAS, 2001,98(21):11879-11884.
    [21] Murali R, Cheng X, Berezov A,et al. Disabling TNF receptor signaling by induced conformational perturbation of tryptophan-107[J]. PNAS,2005,102(31):10970-10975.
  • 加载中
通讯作者: 陈斌, bchen63@163.com
  • 1. 

    沈阳化工大学材料科学与工程学院 沈阳 110142

  1. 本站搜索
  2. 百度学术搜索
  3. 万方数据库搜索
  4. CNKI搜索

Article Metrics

Article views(3782) PDF downloads(685) Cited by()

Related
Proportional views

Research advance of selective inhibitor of tumornecrosis factor receptor

doi: 10.3969/j.issn.1006-0111.2015.05.003

Abstract: TNF signaling pathway was a valuable target, and anti-TNF drugs were successfully used to treat autoimmune and inflammatory diseases.But this therapy abrogate some beneficial TNF signaling, leading to increased risk of infection and malignancy, and the onset of new auto-immune diseases. Inhibiting the soluble TNF/TNFR1 axis while saving the beneficial transmembrane TNF/TNFR2 signaling untouched was a new approach.Because it inhibited the pathological effects of TNF and reduced the side effects, and opened the way for the treatment of other diseases in which TNFR2 inhibition was detrimental.The significance of the selective inhibition of TNFR1-mediated signaling pathways for TNF-related diseases was discussed and the mechanism of TNF identification TNFR was clarified, which might provide new ideas for the design of new drugs.

JIANG Hailong, WANG Ningyuan, LU Yiming. Research advance of selective inhibitor of tumornecrosis factor receptor[J]. Journal of Pharmaceutical Practice and Service, 2015, 33(5): 392-395. doi: 10.3969/j.issn.1006-0111.2015.05.003
Citation: JIANG Hailong, WANG Ningyuan, LU Yiming. Research advance of selective inhibitor of tumornecrosis factor receptor[J]. Journal of Pharmaceutical Practice and Service, 2015, 33(5): 392-395. doi: 10.3969/j.issn.1006-0111.2015.05.003
Reference (21)

Catalog

    /

    DownLoad:  Full-Size Img  PowerPoint
    Return
    Return