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利用吸附在激光微结构硅支架上的体外抗原脉冲巨噬细胞进行可植入疫苗的研发。

Implantable vaccine development using in vitro antigen-pulsed macrophages absorbed on laser micro-structured Si scaffolds.

作者信息

Zerva Ioanna, Simitzi Chara, Siakouli-Galanopoulou Alexandra, Ranella Anthi, Stratakis Emmanuel, Fotakis Costas, Athanassakis Irene

机构信息

Department of Biology, University of Crete, Vassilika Vouton, Heraklion 71409, Crete, Greece.

Department of Biology, University of Crete, Vassilika Vouton, Heraklion 71409, Crete, Greece; Institute of Electronic Structure and Laser (IESL), Foundation for Research and Technology, Vassilika Vouton, Heraklion 71409, Crete, Greece.

出版信息

Vaccine. 2015 Jun 17;33(27):3142-9. doi: 10.1016/j.vaccine.2015.04.017. Epub 2015 May 13.

Abstract

To overcome the limiting antigenic repertoire of protein sub-units and the side effects of adjuvants applied in second generation vaccines, the present work combined in vitro and in vivo manipulations to develop biomaterials allowing natural antigen-loading and presentation in vitro and further activation of the immune response in vivo. 3-dimensional laser micro-textured implantable Si-scaffolds supported mouse macrophage adherence, allowed natural seeding with human serum albumin (antigen) and specific antibody and inflammatory cytokine production in vitro. Implantation of Si-scaffolds loaded with antigen-activated macrophages induced an inflammatory reaction along with antigen-specific antibody production in vivo, which could be detected even 30 days post implantation. Analysis of implant histology using scanning electron microscopy showed that Si-scaffolds could be stable for a 6-month period. Such technology leads to personalized implantable vaccines, opening novel areas of research and treatment.

摘要

为克服蛋白质亚基有限的抗原库以及第二代疫苗中佐剂的副作用,本研究结合了体外和体内操作,以开发能够在体外实现天然抗原加载和呈递,并在体内进一步激活免疫反应的生物材料。三维激光微纹理化的可植入硅支架支持小鼠巨噬细胞黏附,允许在体外天然接种人血清白蛋白(抗原)以及产生特异性抗体和炎性细胞因子。植入负载有抗原激活巨噬细胞的硅支架可在体内引发炎症反应并产生抗原特异性抗体,甚至在植入后30天仍可检测到。使用扫描电子显微镜对植入物组织学进行分析表明,硅支架在6个月内可保持稳定。这种技术可实现个性化可植入疫苗,开辟了新的研究和治疗领域。

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