首页> 美国卫生研究院文献>EMBO Molecular Medicine >Antigen delivery by filamentous bacteriophage fd displaying an anti-DEC-205 single-chain variable fragment confers adjuvanticity by triggering a TLR9-mediated immune response
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Antigen delivery by filamentous bacteriophage fd displaying an anti-DEC-205 single-chain variable fragment confers adjuvanticity by triggering a TLR9-mediated immune response

机译:展示抗DEC-205单链可变片段的丝状噬菌体fd的抗原递送通过触发TLR9介导的免疫反应而赋予佐剂性

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摘要

Filamentous bacteriophage fd particles delivering antigenic determinants via DEC-205 (fdsc-αDEC) represent a powerful delivery system that induces CD8+ T-cell responses even when administered in the absence of adjuvants or maturation stimuli for dendritic cells. In order to investigate the mechanisms of this activity, RNA-Sequencing of fd-pulsed dendritic cells was performed. A significant differential expression of genes involved in innate immunity, co-stimulation and cytokine production was observed. In agreement with these findings, we demonstrate that induction of proinflammatory cytokines and type I interferon by fdsc-αDEC was MYD88 mediated and TLR9 dependent. We also found that fdsc-αDEC is delivered into LAMP-1-positive compartments and co-localizes with TLR9. Thus, phage particles containing a single-strand DNA genome rich in CpG motifs delivered via DEC-205 are able to intercept and trigger the active TLR9 innate immune receptor into late endosome/lysosomes and to enhance the immunogenicity of the displayed antigenic determinants. These findings make fd bacteriophage a valuable tool for immunization without administering exogenous adjuvants.
机译:经由DEC-205(fdsc-αDEC)传递抗原决定簇的丝状噬菌体fd颗粒代表了强大的传递系统,即使没有树突状细胞的佐剂或成熟刺激剂给药,它也能诱导CD8 + T细胞反应。为了研究这种活性的机制,进行了fd脉冲树突状细胞的RNA测序。观察到与先天免疫,共刺激和细胞因子产生有关的基因的显着差异表达。与这些发现一致,我们证明fdsc-αDEC诱导促炎性细胞因子和I型干扰素是MYD88介导的和TLR9依赖性的。我们还发现,fdsc-αDEC被递送至LAMP-1阳性区室并与TLR9共定位。因此,包含富含通过DEC-205传递的CpG基序的单链DNA基因组的噬菌体颗粒能够拦截并触发活性TLR9先天免疫受体进入晚期内体/溶酶体,并增强展示的抗原决定簇的免疫原性。这些发现使fd噬菌体成为无需给予外源佐剂免疫的重要工具。

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