HVEM/LIGHT/BTLA/CD160 cosignaling pathways as targets for immune regulation
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del Rio, M. L.
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Inst Biomed, Immunobiol Lab, Leon, SpainInst Biomed, Immunobiol Lab, Leon, Spain
del Rio, M. L.
[1
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Lucas, C. L.
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Harvard Univ, Massachusetts Gen Hosp, Bone Marrow Transplantat Sect,Sch Med, Transplantat Biol Res Ctr, Boston, MA USAInst Biomed, Immunobiol Lab, Leon, Spain
Lucas, C. L.
[2
]
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Buhler, L.
[2
,3
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Rayat, G.
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Univ Alberta, Fac Med & Dent, Alberta Diabet Inst, Edmonton, AB, CanadaInst Biomed, Immunobiol Lab, Leon, Spain
Rayat, G.
[4
]
Rodriguez-Barbosa, J. I.
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Inst Biomed, Immunobiol Lab, Leon, SpainInst Biomed, Immunobiol Lab, Leon, Spain
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
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.