首页> 外文学位 >Mechanism of biomaterial adjuvant effect: Phenotype of dendritic cells upon biomaterial contact.
【24h】

Mechanism of biomaterial adjuvant effect: Phenotype of dendritic cells upon biomaterial contact.

机译:生物材料佐剂作用的机制:生物材料接触后树突状细胞的表型。

获取原文
获取原文并翻译 | 示例

摘要

Development of combination products such as tissue engineered constructs which combine biomaterials with biologics has prompted the need to clarify the role of biomaterial in potentiating the immune response towards the biological component due to adjuvant effect. In tissue engineering applications, immune responses are to be minimized while vaccine strategies seek to enhance the protective immune response. Thesis project presented herein showed that adjuvant effect of poly(lactic-co-glycolic acid) (PLGA) is mediated in part by maturation of dendritic cells (DCs), immune cells that orchestrate adaptive immune response. Maturation of human peripheral blood monocyte-derived DCs in response to PLGA contact was demonstrated in vitro and in vivo by increased co-stimulatory and MHC molecule expression, mixed lymphocyte reaction, cytokine release, and delayed type hypersensitivity reaction. In contrast to PLGA, agarose did not induce DC maturation, in accordance with its low inflammatory effect. Roles of various receptors involved in DC maturation and recognition of biomaterials were assessed by in vitro receptor blocking studies. In particular, role of Toll-like receptors were further investigated using DCs derived from bone marrows of murine model of Toll-like receptor 4 deficiency (C3H/HeJ). While PLGA induced maturation of DCs from C57BL6 mice, maturation was not observed in DCs from C3H/HeJ strain or control strain, C3H/HeOuJ, perhaps due to particular haplotypes of these animals. Collectively, these results establish the differential adjuvant effects of agarose and PLGA on the level of DC maturation, and begin to elucidate the mechanisms of biomaterial adjuvant effect. In addition, assays developed herein provide methods to screen for biomaterials to be used in combination products, such that biomaterials with desired levels of adjuvanticity as measured by DC maturation effects may be selected for given application.
机译:结合产品的开发,例如将生物材料与生物制剂结合的组织工程构建体,促使人们需要阐明生物材料在增强佐剂作用下对生物成分的免疫反应中的作用。在组织工程应用中,应尽量减少免疫反应,而疫苗策略则旨在增强保护性免疫反应。本文提出的论文项目显示,聚乳酸-乙醇酸共聚物(PLGA)的佐剂作用部分通过树突状细胞(DCs)(负责协调适应性免疫应答的免疫细胞)的成熟来介导。通过增加共刺激和MHC分子表达,混合淋巴细胞反应,细胞因子释放和迟发型超敏反应,在体外和体内证明了人外周血单核细胞衍生的DCs对PLGA接触的成熟。与PLGA相比,琼脂糖根据其低发炎作用不会诱导DC成熟。通过体外受体阻断研究评估了参与DC成熟和生物材料识别的各种受体的作用。特别地,使用来源于Toll样受体4缺乏症(C3H / HeJ)的小鼠模型的骨髓的DC进一步研究了Toll样受体的作用。尽管PLGA诱导了C57BL6小鼠DC的成熟,但在C3H / HeJ菌株或对照菌株C3H / HeOuJ的DC中未观察到成熟,可能是由于这些动物的特定单倍型所致。这些结果共同建立了琼脂糖和PLGA对DC成熟水平的不同佐剂作用,并开始阐明生物材料佐剂作用的机制。另外,本文开发的测定法提供了筛选要在组合产品中使用的生物材料的方法,从而对于给定的应用可以选择具有期望的佐剂水平的生物材料,如通过DC成熟作用测量的。

著录项

  • 作者

    Yoshida, Mutsumi.;

  • 作者单位

    Georgia Institute of Technology.;

  • 授予单位 Georgia Institute of Technology.;
  • 学科 Engineering Biomedical.
  • 学位 Ph.D.
  • 年度 2005
  • 页码 209 p.
  • 总页数 209
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物医学工程;
  • 关键词

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号