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首页> 外文期刊>Clinical & developmental immunology. >Antitumor Effect of KML-B-Treated Dendritic Cells via Induction of Lymphocyte Activation
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Antitumor Effect of KML-B-Treated Dendritic Cells via Induction of Lymphocyte Activation

机译:KML-B处理的树突状细胞通过诱导淋巴细胞活化的抗肿瘤作用。

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摘要

Lectins are carbohydrate-binding proteins with various biological activities, such as antitumor and immunomodulatory effects. Although lectins have various biological activities, they are still limited by cytotoxicity in normal cells. To overcome this problem, we used the noncytotoxic part of Korean mistletoe lectin B-chain (KML-B) to induce maturation of dendritic cells (DCs). A previous study reported that KML-B induces DC maturation by triggering TLR-4, including expression of costimulatory molecules (CD40, CD80, and CD86), MHC II, and secretion of cytokines in DCs. Additionally, matured DCs by KML-B induced T helper (Th) cell activation and differentiation toward Th1 cells. However, the interaction of KML-B-treated DCs with CD8~(+) T cells is still poorly understood. In this study, we confirmed the ability of matured DCs by KML-B to stimulate cytotoxic T cells using OT-1 mouse-derived CD8~(+) T cells. KML-B induced MHC I expression in DCs, stimulation of CD8~(+) T cell activation and proliferation, and IFN- γ secretion. Moreover, tumor sizes were reduced by KML-B treatment during vaccination of OVA_(257?264)-pulsed DCs. Here, we confirmed induction of CD8~(+) T cell activation and the antitumor effect of KML-B treatment in DCs.
机译:凝集素是具有各种生物活性,例如抗肿瘤和免疫调节作用的碳水化合物结合蛋白。尽管凝集素具有多种生物学活性,但它们仍受到正常细胞中细胞毒性的限制。为了克服这个问题,我们使用了韩国槲寄生凝集素B链(KML-B)的非细胞毒性部分来诱导树突状细胞(DC)的成熟。先前的研究报道,KML-B通过触发TLR-4来诱导DC成熟,其中包括共刺激分子(CD40,CD80和CD86),MHC II的表达以及DC中细胞因子的分泌。此外,通过KML-B形成的成熟DC诱导T辅助(Th)细胞激活并向Th1细胞分化。然而,对KML-B处理的DCs与CD8〜(+)T细胞的相互作用仍然知之甚少。在这项研究中,我们证实了KML-B使用OT-1小鼠衍生的CD8〜(+)T细胞刺激DC产生细胞毒性T细胞的能力。 KML-B诱导DC中MHC I表达,刺激CD8〜(+)T细胞活化和增殖以及IFN-γ分泌。此外,在接种OVA_(257?264)脉冲的DC的过程中,通过KML-B治疗可减少肿瘤大小。在这里,我们证实了在DC中诱导CD8〜(+)T细胞活化和KML-B治疗的抗肿瘤作用。

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