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Native cellulose nanofibrills induce immune tolerance in vitro by acting on dendritic cells

机译:天然纤维素纳米纤丝通过作用于树突状细胞体外诱导免疫耐受

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Cellulose nanofibrills (CNFs) are attractive biocompatible, natural nanomaterials for wide biomedical applications. However, the immunological mechanisms of CNFs have been poorly investigated. Considering that dendritic cells (DCs) are the key immune regulatory cells in response to nanomaterials, our aim was to investigate the immunological mechanisms of CNFs in a model of DC-mediated immune response. We found that non-toxic concentrations of CNFs impaired the differentiation, and subsequent maturation of human monocyte-derived (mo)-DCs. In a co-culture with CD4(+)T cells, CNF-treated mo-DCs possessed a weaker allostimulatory and T helper (Th)1 and Th17 polarizing capacity, but a stronger capacity to induce Th2 cells and CD4(+)CD25(hi)FoxP3(hi) regulatory T cells. This correlated with an increased immunoglobulin-like transcript-4 and indolamine dioxygenase-1 expression by CNF-treated mo-DCs, following the partial internalization of CNFs and the accumulation of CD209 and actin bundles at the place of contacts with CNFs. Cumulatively, we showed that CNFs are able to induce an active immune tolerance by inducing tolerogenic DCs, which could be beneficial for the application of CNFs in wound healing and chronic inflammation therapies.
机译:纤维素纳米原纤维(CNF)是有吸引力的生物相容性天然纳米材料,可广泛用于生物医学领域。但是,CNFs的免疫机制尚未得到充分研究。考虑到树突状细胞(DC)是响应纳米材料的关键免疫调节细胞,我们的目的是在DC介导的免疫应答模型中研究CNF的免疫机制。我们发现无毒浓度的CNF会损害分化,以及随后人类单核细胞衍生(mo)-DC的成熟。与CD4(+)T细胞共培养时,经CNF处理的mo-DC具有更弱的同种刺激和T辅助(Th)1和Th17极化能力,但诱导Th2细胞和CD4(+)CD25( hi)FoxP3(hi)调节性T细胞。在CNF部分内在化以及CD209和肌动蛋白束在与CNF接触的位置积聚之后,这与CNF处理过的mo-DCs增加的免疫球蛋白样转录物4和吲哚胺双加氧酶1表达有关。累积地,我们表明CNF能够通过诱导致耐受性DC来诱导主动的免疫耐受,这可能有益于CNF在伤口愈合和慢性炎症治疗中的应用。

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