PLGA公司
透明质酸
生物材料
生物相容性
材料科学
树突状细胞
CD86
壳聚糖
细胞生物学
生物医学工程
免疫系统
琼脂糖
免疫学
化学
纳米技术
生物
生物化学
医学
T细胞
解剖
纳米颗粒
冶金
作者
Julia E. Babensee,Abhijit Paranjpe
摘要
Abstract Immature dendritic cells (iDCs) were derived from human peripheral blood monocytes, and treated with films of biomaterials commonly used in combination products (e.g., tissue engineered constructs or vaccines) to assess the resultant dendritic cell (DC) maturation compared to positive control of lipopolysaccharide (LPS) treatment for DC maturation or negative control of untreated iDCs. The following biomaterials were tested: alginate, agarose, chitosan, hyaluronic acid, 75:25 poly(lactic‐ co ‐glycolic acid) (PLGA). The effect of DC culture on these films was undertaken to identify biomaterials which support DC maturation and those biomaterials that did not. Dendritic cells treated with chitosan or PLGA (agarose to a lesser extent) films increased expression levels of CD86, CD40, and HLA‐DQ, compared to control iDCs, similar to LPS‐matured DCs, whereas DCs treated with alginate or hyaluronic acid films decreased their expression levels of these same molecules. In summary, a differential effect of the biomaterial on which iDCs were cultured was observed as far as the extent of induced DC maturation. The effect of biomaterials on DC maturation, and the associated adjuvant effect, is a novel biocompatibility selection and design criteria for biomaterials to be used in combination products in which immune consequences are potential complications or outcomes. © 2005 Wiley Periodicals, Inc. J Biomed Mater Res, 2005
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