Pathogen-associated molecular patterns on biomaterials: a paradigm for engineering new vaccines

被引:124
作者
Demento, Stacey L. [1 ]
Siefert, Alyssa L. [1 ]
Bandyopadhyay, Arunima [1 ]
Sharp, Fiona A. [1 ]
Fahmy, Tarek M. [1 ]
机构
[1] Yale Univ, Malone Engn Ctr, Dept Biomed Engn, New Haven, CT 06511 USA
关键词
CONTROLLED-RELEASE MICROPARTICLES; B SURFACE-ANTIGEN; CD8(+) T-CELLS; NF-KAPPA-B; IMMUNE-RESPONSE; DENDRITIC CELLS; DELIVERY-SYSTEMS; BETA-GLUCAN; MURAMYL DIPEPTIDE; MUCOSAL VACCINES;
D O I
10.1016/j.tibtech.2011.02.004
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Vaccine development has progressed significantly and has moved from whole microorganisms to subunit vaccines that contain only their antigenic proteins. Subunit vaccines are often less immunogenic than whole pathogens; therefore, adjuvants must amplify the immune response, ideally establishing both innate and adaptive immunity. Incorporation of antigens into biomaterials, such as liposomes and polymers, can achieve a desired vaccine response. The physical properties of these platforms can be easily manipulated, thus allowing for controlled delivery of immunostimulatory factors and presentation of pathogen-associated molecular patterns (PAMPs) that are targeted to specific immune cells. Targeting antigen to immune cells via PAMP-modified biomaterials is a new strategy to control the subsequent development of immunity and, in turn, effective vaccination. Here, we review the recent advances in both immunology and biomaterial engineering that have brought particulate-based vaccines to reality.
引用
收藏
页码:294 / 306
页数:13
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