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生物陶瓷增强过继性免疫治疗中免疫细胞的抗肿瘤活性

英文原题:Bioceramics Enhance the Anti-Tumor Activity of Immune Cells in Adoptive Immunotherapy.

查看英文原题

Bioceramics Enhance the Anti-Tumor Activity of Immune Cells in Adoptive Immunotherapy.

PubMed 2024/09/30(内容时间) Int J Mol Sci Q1 · IF 5.6(JCR 2025)

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中文摘要

近年来的研究聚焦于无副作用的免疫疗法作为一种创新的癌症医学治疗方法。然而,典型的免疫疗法药物非常昂贵。在此,我们提出使用免疫陶瓷,通过与其表面接触来激活免疫细胞。先前的研究表明,含有苯硼酸基团的聚合物可以激活淋巴细胞。这种激活可能是由于细胞中的糖链与BO 2 基团解离形成的B(OH) 3 中的OH基团之间的相互作用。我们已经阐明,含硼磷灰石(BAp)在体外可激活淋巴细胞。在本研究中,我们使用CaO-P 2 O 5 -SiO 2 -B 2 O 3 体系(CPSB陶瓷)制备了以BAp为主晶相的陶瓷表面。体外评估结果表明,与CPSB陶瓷共培养的脾细胞中杀伤性T细胞数量多于在对照表面共培养的脾细胞。体内评估结果表明,当CD8阳性T细胞在单个陶瓷上培养并随后注射到荷瘤小鼠体内时,CPSB陶瓷显著抑制了肿瘤生长。目前的CPSB陶瓷有望成为免疫治疗中有价值的生物材料。

展开英文摘要原文

Recent research has focused on immunotherapy with no side effects as an innovative medical treatment for cancer.

However, typical drugs for immunotherapy are very expensive.

Here, we propose the use of immunoceramics that activate immune cells by contact with their surface. Previous studies demonstrated that polymers, including the phenylboronic acid group, could activate lymphocytes. This activation may be due to the interaction between the sugar chains in cells and the OH group in B(OH) 3 formed via the dissociation of the BO 2 group.

We have clarified that boron-containing apatite (BAp) activated lymphocytes in vitro. In this study, we fabricated the ceramic surfaces using the CaO-P 2 O 5 -SiO 2 -B 2 O 3 system (CPSB ceramics) containing BAp as a main crystalline phase. The results of the in vitro evaluation indicated that killer T cells in splenocytes cocultured with the CPSB ceramics were more numerous than in splenocytes cocultured on a control surface.

The results of the in vivo evaluation indicated that the CPSB ceramics significantly inhibited tumor growth when CD8-positive T cells were cultured on individual ceramics and subsequently injected into tumor-bearing mice. The present CPSB ceramics are expected to be a valuable biomaterial for immunotherapy.

论文信息

作者
Nose M、Nitta A、Zheng Y、Kizukuri R、Nagao Y、Nagai S、Aizawa M
单位
Applied Chemistry Program, Graduate School of Science and Technology, Meiji University, Kawasaki 214-8571, Japan.Japan
期刊
International journal of molecular sciences2024 Sep 30
原文标识
PubMed 39408898 · DOI 10.3390/ijms251910567