Hydrogels and Scaffolds for Immunomodulation

被引:295
作者
Singh, Ankur [1 ]
Peppas, Nicholas A. [2 ,3 ]
机构
[1] Cornell Univ, Sibley Sch Mech & Aerosp Engn, Ithaca, NY 14853 USA
[2] Univ Texas Austin, Dept Chem Engn, Dept Biomed Engn, Austin, TX 78712 USA
[3] Univ Texas Austin, Coll Pharm, Austin, TX 78712 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
immunology; hydrogels; biomaterials; scaffolds; immunomodulation; polymers; REGULATORY T-CELLS; IMMUNOSUPPRESSIVE TUMOR MICROENVIRONMENT; DEGRADABLE DEXTRAN HYDROGELS; THERMAL-SENSITIVE HYDROGEL; HEPATITIS-B-VACCINE; IN-SITU; DENDRITIC CELLS; CONTROLLED-RELEASE; IMMUNE-RESPONSES; HYALURONIC-ACID;
D O I
10.1002/adma.201402105
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
For over two decades, immunologists and biomaterials scientists have co-existed in parallel world with the rationale of understanding the molecular profile of immune responses to vaccination, implantation, and treating incurable diseases. Much of the field of biomaterial-based immunotherapy has relied on evaluating model antigens such as chicken egg ovalbumin in mouse models but their relevance to humans has been point of much discussion. Nevertheless, such model antigens have provided important insights into the mechanisms of immune regulation and served as a proof-of-concept for plethora of biomaterial-based vaccines. After years of extensive development of numerous biomaterials for immunomodulation, it is only recently that an experimental scaffold vaccine implanted beneath the skin has begun to use the human model to study the immune responses to cancer vaccination by co-delivering patient-derived tumor lysates and immunomodulatory proteins. If successful, this scaffold vaccine will change the way we approached untreatable cancers, but more importantly, will allow a faster and more rational translation of therapeutic regimes to other cancers, chronic infections, and autoimmune diseases. Most materials reviews have focused on immunomodulatory adjuvants and micro-nano-particles. Here we provide an insight into emerging hydrogel and scaffold based immunomodulatory approaches that continue to demonstrate efficacy against immune associated diseases.
引用
收藏
页码:6530 / 6541
页数:12
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