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展示四跨膜紧密连接蛋白的包被病毒样颗粒用于癌症免疫治疗。

Displaying Tetra-Membrane Spanning Claudins on Enveloped Virus-Like Particles for Cancer Immunotherapy.

机构信息

Molecular Biotechnology and Gene Therapy, Paul-Ehrlich-Institut, Langen, Germany.

Faculty of Applied Natural Sciences, TH Köln, University of Applied Sciences Cologne, Leverkusen, Germany.

出版信息

Biotechnol J. 2018 Mar;13(3):e1700345. doi: 10.1002/biot.201700345. Epub 2017 Nov 23.

Abstract

Virus-like particles (VLPs) displaying foreign antigens have become an important tool in vaccination including the induction of immune responses against self-antigens. Claudin 6 (CLDN6) has been identified as tumor-associated antigen and is therefore a potential target for tumor vaccination strategies. However, as tetra-membrane spanning protein its incorporation into VLPs while preserving a native fold is challenging. Here, we attempted the incorporation of a panel of engineered CLDN6 variants into the membrane of retrovirus-derived VLPs. Interestingly, wild-type CLDN6 revealed the most efficient display. VLPs presenting CLDN6 or CLDN9 derived from different donor species were produced and preservation of their native confirmation was demonstrated by antibody binding assays. VLPs displaying murine CLDN6 were used to immunize mice. Antibodies recognizing native CLDN6 as displayed on cell surfaces and mediating complement-dependent cytotoxicity were elicited in vaccinated animals. The data suggest applications of CLDN6 displaying VLPs in cancer immunotherapy.

摘要

病毒样颗粒(VLPs)展示外源抗原已成为接种疫苗的重要工具,包括诱导针对自身抗原的免疫反应。Claudin 6(CLDN6)已被确定为肿瘤相关抗原,因此是肿瘤疫苗接种策略的潜在靶点。然而,作为四跨膜蛋白,将其纳入 VLPs 中同时保持天然构象具有挑战性。在这里,我们尝试将一组工程化的 CLDN6 变体纳入逆转录病毒衍生的 VLPs 的膜中。有趣的是,野生型 CLDN6 显示出最有效的展示。展示来自不同供体物种的 CLDN6 或 CLDN9 的 VLPs 被制备,并通过抗体结合测定证明了它们天然构象的保留。展示小鼠 CLDN6 的 VLPs 被用于免疫小鼠。在接种疫苗的动物中,诱导出了识别细胞表面展示的天然 CLDN6 并介导补体依赖性细胞毒性的抗体。这些数据表明,展示 CLDN6 的 VLPs 在癌症免疫治疗中有应用前景。

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