Department of Microbiology and Immunology and 2 Department of Surgery, 3 Diabetes Research Institute, University of Miami Miller School of Medicine, Miami, FL 33136 4 Department of Biomedical Engineering, University of Miami, Coral Gables, FL 33124.
J Exp Med. 2014 Mar 10;211(3):441-56. doi: 10.1084/jem.20130785. Epub 2014 Feb 24.
Real-time imaging studies are reshaping immunological paradigms, but a visual framework is lacking for self-antigen-specific T cells at the effector phase in target tissues. To address this issue, we conducted intravital, longitudinal imaging analyses of cellular behavior in nonlymphoid target tissues to illustrate some key aspects of T cell biology. We used mouse models of T cell-mediated damage and protection of pancreatic islet grafts. Both CD4(+) and CD8(+) effector T (Teff) lymphocytes directly engaged target cells. Strikingly, juxtaposed β cells lacking specific antigens were not subject to bystander destruction but grew substantially in days, likely by replication. In target tissue, Foxp3(+) regulatory T (Treg) cells persistently contacted Teff cells with or without involvement of CD11c(+) dendritic cells, an observation conciliating with the in vitro "trademark" of Treg function, contact-dependent suppression. This study illustrates tolerance induction by contact-based immune cell interaction in target tissues and highlights potentials of tissue regeneration under antigenic incognito in inflammatory settings.
实时成像研究正在重塑免疫学范式,但在靶组织中的效应阶段,针对自身抗原特异性 T 细胞,仍然缺乏可视化框架。为了解决这个问题,我们对非淋巴组织靶器官中的细胞行为进行了活体、纵向成像分析,以阐明 T 细胞生物学的一些关键方面。我们使用了 T 细胞介导的胰岛移植物损伤和保护的小鼠模型。CD4(+)和 CD8(+)效应 T (Teff)淋巴细胞均直接与靶细胞相互作用。引人注目的是,相邻的缺乏特定抗原的β细胞不会受到旁观者破坏,但在数天内大量生长,可能通过复制。在靶组织中,Foxp3(+)调节性 T (Treg)细胞持续与 Teff 细胞接触,无论是否涉及 CD11c(+)树突状细胞,这一观察结果与体外 Treg 功能的“商标”,即接触依赖性抑制相一致。这项研究说明了在靶组织中基于接触的免疫细胞相互作用诱导耐受的机制,并强调了在炎症环境下抗原隐匿性下组织再生的潜力。