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

被引:105
作者
Babensee, JE
Paranjpe, A
机构
[1] Georgia Inst Technol, Wallace H Coulter Dept Biomed Engn, Atlanta, GA 30332 USA
[2] Georgia Inst Technol, Dept Biomed Engn, Atlanta, GA 30332 USA
[3] Emory Univ, Atlanta, GA 30332 USA
关键词
biomaterial; dendritic cells; maturation; adjuvant;
D O I
10.1002/jbm.a.30429
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
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. (c) 2005 Wiley Periodicals, Inc.
引用
收藏
页码:503 / 510
页数:8
相关论文
共 66 条
[1]   Toll-like receptors in the induction of the innate immune response [J].
Aderem, A ;
Ulevitch, RJ .
NATURE, 2000, 406 (6797) :782-787
[2]   Immunobiology of dendritic cells [J].
Banchereau, J ;
Briere, F ;
Caux, C ;
Davoust, J ;
Lebecque, S ;
Liu, YT ;
Pulendran, B ;
Palucka, K .
ANNUAL REVIEW OF IMMUNOLOGY, 2000, 18 :767-+
[3]   Dendritic cells and the control of immunity [J].
Banchereau, J ;
Steinman, RM .
NATURE, 1998, 392 (6673) :245-252
[4]   The effect of the physical form of poly(lactic-co-glycolic acid) carriers on the humoral immune response to co-delivered antigen [J].
Bennewitz, NL ;
Babensee, JE .
BIOMATERIALS, 2005, 26 (16) :2991-2999
[5]  
COLTON CK, 1991, T ASME, V113, P152
[6]  
de Chalain T, 1999, J BIOMED MATER RES, V44, P280, DOI 10.1002/(SICI)1097-4636(19990305)44:3<280::AID-JBM6>3.0.CO
[7]  
2-H
[8]  
Ding ZM, 1999, J IMMUNOL, V163, P5029
[9]   Immune escape through C-type lectins on dendritic cells [J].
Engering, A ;
Geijtenbeek, TBH ;
van Kooyk, Y .
TRENDS IN IMMUNOLOGY, 2002, 23 (10) :480-485
[10]   Poly(DL-lactide-co-glycolide) microspheres as carriers for peptide vaccines [J].
Ertl, HCJ ;
Varga, I ;
Xiang, ZQ ;
Kaiser, K ;
Stephens, LD ;
Otvos, L .
VACCINE, 1996, 14 (09) :879-885