HVEM/LIGHT/BTLA/CD160 cosignaling pathways as targets for immune regulation

被引:130
作者
del Rio, M. L. [1 ]
Lucas, C. L. [2 ]
Buhler, L. [2 ,3 ]
Rayat, G. [4 ]
Rodriguez-Barbosa, J. I. [1 ]
机构
[1] Inst Biomed, Immunobiol Lab, Leon, Spain
[2] Harvard Univ, Massachusetts Gen Hosp, Bone Marrow Transplantat Sect,Sch Med, Transplantat Biol Res Ctr, Boston, MA USA
[3] Univ Hosp Geneva, Dept Surg, Surg Res Unit, Geneva, Switzerland
[4] Univ Alberta, Fac Med & Dent, Alberta Diabet Inst, Edmonton, AB, Canada
关键词
coinhibition; costimulation; transplantation; autoimmunity; T-LYMPHOCYTE ATTENUATOR; HERPESVIRUS ENTRY MEDIATOR; FACTOR RECEPTOR SUPERFAMILY; LYMPHOTOXIN-BETA RECEPTOR; MHC CLASS-I; B-LYMPHOCYTE; CELL-ACTIVATION; TNF SUPERFAMILY; FAMILY-MEMBER; NK CELLS;
D O I
10.1189/jlb.0809590
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Immunosuppression is currently the treatment of choice to attenuate the chronic deterioration of tissue function as a result of the effector mechanisms of the immunological response in transplant rejection and autoimmune diseases. However, global immunosuppression greatly increases the risk of acquiring life-threatening infections and is associated with organ toxicity when used long-term. Thus, alternative approaches that inhibit only the unwanted immune responses and preserve general immunity are highly desirable. The receptor/ligand pairs involved in the cross-talk between DC and T cells have been the focus of intense and exciting research during the last decade. The HVEM/LIGHT/BTLA/CD160 costimulatory/coinhibitory pathway has emerged as a potential target for the development of immune therapeutic interventions. Herein, we will summarize and discuss how blockade of the costimulatory HVEM/LIGHT interaction or agonist signaling through the inhibitory BTLA and CD160 receptors could contribute to the control of deleterious immune responses. J. Leukoc. Biol. 87: 223-235; 2010.
引用
收藏
页码:223 / 235
页数:13
相关论文
共 95 条
  • [1] Functional diversity of helper T lymphocytes
    Abbas, AK
    Murphy, KM
    Sher, A
    [J]. NATURE, 1996, 383 (6603) : 787 - 793
  • [2] Identification of a novel CD160+ CD4+ T-lymphocyte subset in the skin:: A possible role for CD160 in skin inflammation
    Abecassis, Sofia
    Giustiniani, Jerome
    Meyer, Nicolas
    Schiavon, Valerie
    Ortonne, Nicolas
    Campillo, Jose A.
    Bagot, Martine
    Bensussan, Armand
    [J]. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2007, 127 (05) : 1161 - 1166
  • [3] The role of TNF receptor and TNF superfamily molecules in organ transplantation
    Adams, AB
    Larsen, CP
    Pearson, TC
    Newell, KA
    [J]. AMERICAN JOURNAL OF TRANSPLANTATION, 2002, 2 (01) : 12 - 18
  • [4] Agrawal S, 1999, J IMMUNOL, V162, P1223
  • [5] Anumanthan A, 1998, J IMMUNOL, V161, P2780
  • [6] T-CELL SUBSETS, BM MUTANTS, AND THE MECHANISMS OF ALLOGENEIC SKIN-GRAFT REJECTION
    AUCHINCLOSS, H
    MAYER, T
    GHOBRIAL, R
    WINN, HJ
    [J]. IMMUNOLOGIC RESEARCH, 1989, 8 (02) : 149 - 164
  • [7] Cutting edge: Engagement of CD160 by its HLA-C physiological ligand triggers a unique cytokine profile secretion in the cytotoxic peripheral blood NK cell subset
    Barakonyi, A
    Rabot, M
    Marie-Cardine, A
    Aguerre-Girr, M
    Polgar, B
    Schiavon, V
    Bensussan, A
    Le Bouteiller, P
    [J]. JOURNAL OF IMMUNOLOGY, 2004, 173 (09) : 5349 - 5354
  • [8] Restoring function in exhausted CD8 T cells during chronic viral infection
    Barber, DL
    Wherry, EJ
    Masopust, D
    Zhu, BG
    Allison, JP
    Sharpe, AH
    Freeman, GJ
    Ahmed, R
    [J]. NATURE, 2006, 439 (7077) : 682 - 687
  • [9] Immunomodulation with CTLA4-Ig in islet transplantation
    Benhamou, PY
    [J]. TRANSPLANTATION, 2002, 73 (01) : S40 - S42
  • [10] Blockade of programmed death-1 engagement accelerates graft-versus-host disease lethality by an IFN-γ-dependent mechanism
    Blazar, BR
    Carreno, BM
    Panoskaltsis-Mortari, A
    Carter, L
    Iwai, Y
    Yagita, H
    Nishimura, H
    Taylor, PA
    [J]. JOURNAL OF IMMUNOLOGY, 2003, 171 (03) : 1272 - 1277