Differential levels of dendritic cell maturation on different biomaterials used in combination products

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
出处
期刊:Journal of Biomedical Materials Research Part A [Wiley]
卷期号:74A (4): 503-510 被引量:139
标识
DOI:10.1002/jbm.a.30429
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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