Catakovic Kemal, Klieser Eckhard, Neureiter Daniel, Geisberger Roland
Laboratory for Immunological and Molecular Cancer Research, Department of Internal Medicine III with Haematology, Medical Oncology, Haemostaseology, Infectiology and Rheumatology, Oncologic Center, Paracelsus Medical University, Müllner Hauptstrasse 48, Salzburg, 5020, Austria.
Salzburg Cancer Research Institute, Salzburg, Austria.
Cell Commun Signal. 2017 Jan 5;15(1):1. doi: 10.1186/s12964-016-0160-z.
The immune system is capable of distinguishing between danger- and non-danger signals, thus inducing either an appropriate immune response against pathogens and cancer or inducing self-tolerance to avoid autoimmunity and immunopathology. One of the mechanisms that have evolved to prevent destruction by the immune system, is to functionally silence effector T cells, termed T cell exhaustion, which is also exploited by viruses and cancers for immune escape In this review, we discuss some of the phenotypic markers associated with T cell exhaustion and we summarize current strategies to reinvigorate exhausted T cells by blocking these surface marker using monoclonal antibodies.
免疫系统能够区分危险信号和非危险信号,从而诱导针对病原体和癌症的适当免疫反应,或者诱导自身耐受以避免自身免疫和免疫病理。为防止被免疫系统破坏而进化出的一种机制是在功能上使效应T细胞失活,即所谓的T细胞耗竭,病毒和癌症也利用这一机制实现免疫逃逸。在本综述中,我们讨论了一些与T细胞耗竭相关的表型标志物,并总结了目前通过使用单克隆抗体阻断这些表面标志物来恢复耗竭T细胞活力的策略。