首页> 美国卫生研究院文献>Frontiers in Immunology >Gel-Trapped Lymphorganogenic Chemokines Trigger Artificial Tertiary Lymphoid Organs and Mount Adaptive Immune Responses In Vivo
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Gel-Trapped Lymphorganogenic Chemokines Trigger Artificial Tertiary Lymphoid Organs and Mount Adaptive Immune Responses In Vivo

机译:凝胶陷阱的淋巴器官趋化因子触发人工第三级淋巴器官并在体内产生适应性免疫反应。

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摘要

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.
机译:我们以前使用表达淋巴毒素α的基质细胞在小鼠体内产生了人工淋巴结样三级淋巴器官(artTLOs)。在这里,我们通过在不存在淋巴组织组织基质细胞的情况下应用滞留在缓慢释放的凝胶中的可溶性因子来显示可移植和功能性artTLO的构建。所得的artTLOs易于移除,可移植,并能够吸引记忆B和T细胞。重要的是,artTLOs诱导了强大的抗原特异性次级免疫应答,这在免疫受损的宿主中尤其明显。如本文所述的功能稳定的免疫组织/器官的合成可能是最终开发基于免疫系统的疗法的第一步。尽管需要从精确的作用机制中学习很多东西,但它们可能为将来提供重建免疫功能的方法,以克服迄今无法治愈的疾病,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,包括免疫衰老。在老化过程中。

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