Kobayashi Yuka, Watanabe Takeshi
The Tazuke-Kofukai Medical Research Institute, Kitano Hospital, Kita-ku , Osaka , Japan.
Front Immunol. 2016 Aug 22;7:316. doi: 10.3389/fimmu.2016.00316. eCollection 2016.
We previously generated artificial lymph node-like tertiary lymphoid organs (artTLOs) in mice using lymphotoxin α-expressing stromal cells. Here, we show the construction of transplantable and functional artTLOs by applying soluble factors trapped in slow-releasing gels in the absence of lymphoid tissue organizer stromal cells. The resultant artTLOs were easily removable, transplantable, and were capable of attracting memory B and T cells. Importantly, artTLOs induced a powerful antigen-specific secondary immune response, which was particularly pronounced in immune-compromised hosts. Synthesis of functionally stable immune tissues/organs like those described here may be a first step to eventually develop immune system-based therapeutics. Although much needs to be learned from the precise mechanisms of action, they may offer ways in the future to reestablish immune functions to overcome hitherto untreatable diseases, including severe infection, cancer, autoimmune diseases, and various forms of immune deficiencies, including immune-senescence during aging.
我们之前利用表达淋巴毒素α的基质细胞在小鼠体内生成了人工淋巴结样三级淋巴器官(artTLOs)。在此,我们展示了在没有淋巴组织 organizer 基质细胞的情况下,通过应用包裹在缓释凝胶中的可溶性因子构建可移植且有功能的 artTLOs。所得到的 artTLOs 易于移除、可移植,并且能够吸引记忆 B 细胞和 T 细胞。重要的是,artTLOs 诱导了强大的抗原特异性二次免疫反应,这在免疫受损宿主中尤为明显。合成如本文所述的功能稳定的免疫组织/器官可能是最终开发基于免疫系统的治疗方法的第一步。尽管仍需从精确的作用机制中了解很多内容,但它们未来可能提供重新建立免疫功能的方法,以克服包括严重感染、癌症、自身免疫性疾病以及各种形式的免疫缺陷(包括衰老过程中的免疫衰老)等迄今无法治疗的疾病。