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树突状细胞中的早期转录特征以及含 TLR 配体 VLP 免疫诱导保护性 T 细胞应答——CCL2 的作用。

Early Transcriptional Signature in Dendritic Cells and the Induction of Protective T Cell Responses Upon Immunization With VLPs Containing TLR Ligands-A Role for CCL2.

机构信息

The Jenner Institute, Oxford University, Oxford, United Kingdom.

Immunology, Inselspital, Bern, Switzerland.

出版信息

Front Immunol. 2019 Aug 2;10:1679. doi: 10.3389/fimmu.2019.01679. eCollection 2019.

DOI:10.3389/fimmu.2019.01679
PMID:31428084
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6687836/
Abstract

Inducing T cell responses by therapeutic vaccination requires appropriate activation of antigen presenting cells (APCs). The use of virus-like particles (VLPs) containing Toll-like receptor (TLR) ligands has demonstrated remarkable potential in activating APCs and modulating the immune response both for prophylactic vaccines as well as immunotherapy. Here, we employed VLPs associated to TLR ligands as tools to modulate cytotoxic response mediated by CD8 T cells and provide further insight in the development of T cell-based immunotherapy. We have investigated the transcriptional signature in dendritic cells (DCs) from mice immunized with VLPs containing distinct classes of nucleic acid and correlated the expression patterns with the efficiency of induced T cell responses. We identified key pathways activated in DCs that are involved in the appropriated induction of T cell responses and show evidence for the modulatory effect of CCL2 in CD8 T cells responses. These insights shed light on immune networks that are pivotal for the induction of potent cytotoxic T cell responses and identify key genes for appropriate DC activation and subsequent modulation of the adaptive immune response.

摘要

通过治疗性疫苗诱导 T 细胞反应需要适当激活抗原提呈细胞 (APC)。含有 Toll 样受体 (TLR) 配体的病毒样颗粒 (VLPs) 在激活 APC 和调节免疫反应方面具有显著的潜力,无论是预防性疫苗还是免疫疗法。在这里,我们将与 TLR 配体相关的 VLPs 用作工具,以调节 CD8 T 细胞介导的细胞毒性反应,并为基于 T 细胞的免疫疗法的发展提供进一步的见解。我们研究了从小鼠中免疫 VLPs 中分离出的树突状细胞 (DC) 的转录特征,并将表达模式与诱导 T 细胞反应的效率相关联。我们确定了在 DC 中激活的关键途径,这些途径参与了 T 细胞反应的适当诱导,并为 CCL2 在 CD8 T 细胞反应中的调节作用提供了证据。这些见解揭示了诱导有效细胞毒性 T 细胞反应的免疫网络的关键,并确定了适当的 DC 激活和随后调节适应性免疫反应的关键基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62f2/6687836/ee245dc6df85/fimmu-10-01679-g0008.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62f2/6687836/7df7a82d19ae/fimmu-10-01679-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62f2/6687836/565f68d4c265/fimmu-10-01679-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62f2/6687836/a304853f5f32/fimmu-10-01679-g0006.jpg
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