Duraes F V, Thelemann C, Sarter K, Acha-Orbea H, Hugues S, Reith W
Department of Pathology and Immunology, Faculty of Medicine, University of Geneva, Geneva, Switzerland.
Tissue Antigens. 2013 Jul;82(1):1-15. doi: 10.1111/tan.12136.
It is well established that interactions between CD4(+) T cells and major histocompatibility complex class II (MHCII) positive antigen-presenting cells (APCs) of hematopoietic origin play key roles in both the maintenance of tolerance and the initiation and development of autoimmune and inflammatory disorders. In sharp contrast, despite nearly three decades of intensive research, the functional relevance of MHCII expression by non-hematopoietic tissue-resident cells has remained obscure. The widespread assumption that MHCII expression by non-hematopoietic APCs has an impact on autoimmune and inflammatory diseases has in most instances neither been confirmed nor excluded by indisputable in vivo data. Here we review and put into perspective conflicting in vitro and in vivo results on the putative impact of MHCII expression by non-hematopoietic APCs--in both target organs and secondary lymphoid tissues--on the initiation and development of representative autoimmune and inflammatory disorders. Emphasis will be placed on the lacunar status of our knowledge in this field. We also discuss new mouse models--developed on the basis of our understanding of the molecular mechanisms that regulate MHCII expression--that constitute valuable tools for filling the severe gaps in our knowledge on the functions of non-hematopoietic APCs in inflammatory conditions.
众所周知,CD4(+) T细胞与造血来源的主要组织相容性复合体II类(MHCII)阳性抗原呈递细胞(APC)之间的相互作用在维持耐受性以及自身免疫和炎症性疾病的发生和发展中均起着关键作用。与之形成鲜明对比的是,尽管经过近三十年的深入研究,但非造血组织驻留细胞表达MHCII的功能相关性仍不清楚。非造血APC表达MHCII会影响自身免疫和炎症性疾病这一广泛的假设,在大多数情况下,既未得到确凿的体内数据证实,也未被排除。在此,我们回顾并审视关于非造血APC(在靶器官和二级淋巴组织中)表达MHCII对代表性自身免疫和炎症性疾病的发生和发展的假定影响的体外和体内相互矛盾的结果。重点将放在我们在该领域知识的空白状态上。我们还将讨论基于我们对调节MHCII表达的分子机制的理解而开发的新小鼠模型,这些模型是填补我们在炎症条件下非造血APC功能知识严重空白的宝贵工具。