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The signaling networks of the herpesvirus entry mediator (TNFRSF14) in immune regulation.

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  • المؤلفون: Steinberg MW;Steinberg MW; Cheung TC; Ware CF
  • المصدر:
    Immunological reviews [Immunol Rev] 2011 Nov; Vol. 244 (1), pp. 169-87.
  • نوع النشر :
    Journal Article; Research Support, N.I.H., Extramural; Review
  • اللغة:
    English
  • معلومة اضافية
    • المصدر:
      Publisher: Blackwell Country of Publication: England NLM ID: 7702118 Publication Model: Print Cited Medium: Internet ISSN: 1600-065X (Electronic) Linking ISSN: 01052896 NLM ISO Abbreviation: Immunol Rev Subsets: MEDLINE
    • بيانات النشر:
      Publication: <2002-> : Oxford : Blackwell
      Original Publication: Copenhagen, Munksgaard.
    • الموضوع:
    • نبذة مختصرة :
      The tumor necrosis factor (TNF) receptor superfamily member herpesvirus entry mediator (HVEM) (TNFRSF14) regulates T-cell immune responses by activating both inflammatory and inhibitory signaling pathways. HVEM acts as both a receptor for the canonical TNF-related ligands, LIGHT [lymphotoxin-like, exhibits inducible expression, and competes with herpes simplex virus glycoprotein D for HVEM, a receptor expressed on T lymphocytes] and lymphotoxin-α, and as a ligand for the immunoglobulin superfamily proteins BTLA (B and T lymphocyte attenuator) and CD160, a feature distinguishing HVEM from other immune regulatory molecules. The ability of HVEM to interact with multiple ligands in distinct configurations creates a functionally diverse set of intrinsic and bidirectional signaling pathways that control both inflammatory and inhibitory responses. The HVEM system is integrated into the larger LTβR and TNFR network through extensive shared ligand and receptor usage. Experimental mouse models and human diseases indicate that dysregulation of HVEM network may contribute to autoimmune pathogenesis, making it an attractive target for drug intervention.
      (© 2011 John Wiley & Sons A/S.)
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    • Grant Information:
      AI067890 United States AI NIAID NIH HHS; R21 AI088445 United States AI NIAID NIH HHS; R01 AI067890 United States AI NIAID NIH HHS; R37AI33068 United States AI NIAID NIH HHS; R01 AI048074 United States AI NIAID NIH HHS; R01 AI048073 United States AI NIAID NIH HHS; R37 AI033068 United States AI NIAID NIH HHS; AI048074 United States AI NIAID NIH HHS
    • الرقم المعرف:
      0 (Antigens, CD)
      0 (CD160 protein, human)
      0 (GPI-Linked Proteins)
      0 (Lymphotoxin beta Receptor)
      0 (Lymphotoxin-alpha)
      0 (Receptors, Immunologic)
      0 (Receptors, Tumor Necrosis Factor, Member 14)
      0 (TNFRSF14 protein, human)
      0 (Tumor Necrosis Factor Ligand Superfamily Member 14)
      0 (Tumor Necrosis Factor-alpha)
      0 (Viral Envelope Proteins)
      0 (glycoprotein D, Human herpesvirus 1)
    • الموضوع:
      Date Created: 20111025 Date Completed: 20120209 Latest Revision: 20240610
    • الموضوع:
      20240610
    • الرقم المعرف:
      PMC3381650
    • الرقم المعرف:
      10.1111/j.1600-065X.2011.01064.x
    • الرقم المعرف:
      22017438