The simultaneous effect of polymer chemistry and device geometry on the in vitro activation of murine dendritic cells

被引:57
作者
Petersen, Latrisha K. [1 ]
Xue, Li [2 ]
Wannemuehler, Michael J. [3 ]
Rajan, Krishna [2 ]
Narasimhan, Balaji [1 ]
机构
[1] Iowa State Univ, Dept Biol & Chem Engn, Ames, IA 50011 USA
[2] Iowa State Univ, Dept Mat Sci & Engn, Ames, IA 50011 USA
[3] Iowa State Univ, Dept Vet Microbiol & Prevent Med, Ames, IA 50011 USA
关键词
Polyanhydrides; Murine dendritic cells; Adjuvants; Vaccine delivery; Nanospheres; POLY(LACTIC-CO-GLYCOLIC ACID); BIOERODIBLE POLYANHYDRIDES; DRUG-DELIVERY; IMMUNE-RESPONSES; GENE DELIVERY; BONE-MARROW; DC-SIGN; BIOMATERIALS; MATURATION; RELEASE;
D O I
10.1016/j.biomaterials.2009.05.069
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Polyanhydrides are a promising class of biomaterials for use as vaccine adjuvants and as multicomponent implants. Their properties can be tailored for such applications as controlled drug release, drug stability, and/or immune regulation (adjuvant effect). Understanding the induction of immunomodulatory mechanisms of this polymer system is important for the design and development of efficacious vaccines and tissue compatible multi-component implantable devices using this polymer system. This study describes the development of a rapid multiplexed method for the investigation of the adjuvanticity of polyanhydride nanospheres and films using murine dendritic cells (DCs). To assess the immune response, cell surface markers including MHC II, CD86, CD40, and CD209 and cytokines including IL-6, IL-12p40, and IL-10 were measured. The DCs incubated with nanospheres displayed enhanced expression of all the surface markers and the production of IL-12p40 compared to DCs incubated with polymer films in a chemistry-dependent manner. This suggests that polyanhydrides of various chemistries and device geometries can be tailored to achieve desired levels of immune cell activation for specific applications. The observed biocompatibility and activation of DCs by polyanhydride devices supports their inclusion in vaccine delivery devices as well as in multi-component medical implants. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5131 / 5142
页数:12
相关论文
共 48 条
[1]  
Abbas A K., 2005, Cellular and molecular immunology
[2]  
ADLER AF, COMB CHEM H IN PRESS
[3]   Toll-like receptors and innate immunity [J].
Akira, S .
ADVANCES IN IMMUNOLOGY, VOL 78, 2001, 78 :1-56
[4]   Biomaterial microarrays: rapid, microscale screening of polymer-cell interaction [J].
Anderson, DG ;
Putnam, D ;
Lavik, EB ;
Mahmood, TA ;
Langer, R .
BIOMATERIALS, 2005, 26 (23) :4892-4897
[5]   Semi-automated synthesis and screening of a large library of degradable cationic polymers for gene delivery [J].
Anderson, DG ;
Lynn, DM ;
Langer, R .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2003, 42 (27) :3153-3158
[6]   Structure/property studies of polymeric gene delivery using a library of poly(β-amino esters) [J].
Anderson, DG ;
Akinc, A ;
Hossain, N ;
Langer, R .
MOLECULAR THERAPY, 2005, 11 (03) :426-434
[7]   Nanoliter-scale synthesis of arrayed biomaterials and application to human embryonic stem cells [J].
Anderson, DG ;
Levenberg, S ;
Langer, R .
NATURE BIOTECHNOLOGY, 2004, 22 (07) :863-866
[8]  
[Anonymous], Data Mining Practical Machine Learning Tools and Techniques with Java
[9]  
[Anonymous], 1988, Applied Multivariate Statistical Analysis
[10]  
Babensee JE, 2003, CELL TRANSPLANT, V12, P159