Polyphosphazene immunoadjuvants: Historical perspective and recent advances

被引:40
作者
Andrianov, Alexander K. [1 ]
Langer, Robert [2 ,3 ]
机构
[1] Univ Maryland, Inst Biosci & Biotechnol Res, Rockville, MD 20850 USA
[2] MIT, David H Koch Inst Integrat Canc Res, Cambridge, MA 02139 USA
[3] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
Immunoadjuvants; Vaccine delivery; Polyphosphazenes; TLR agonists; Resiquimod; Antigens; Proteins; Nanocomplexes; Biodegradable polymers; VIRUS FUSION PROTEIN; BALANCED IMMUNE-RESPONSES; HOST-DEFENSE PEPTIDE; CROSS-LINKABLE POLYPHOSPHAZENE; INDUCE PROTECTIVE IMMUNITY; AVIAN BETA DEFENSIN; COMBINATION ADJUVANT; CPG OLIGODEOXYNUCLEOTIDES; INTRADERMAL IMMUNIZATION; INTRANASAL IMMUNIZATION;
D O I
10.1016/j.jconrel.2020.12.001
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The development of successful vaccines has been increasingly reliant on the use of immunoadjuvants - additives, which can enhance and modulate immune responses to vaccine antigens. Immunoadjuvants of the polyphosphazene family encompass synthetic biodegradable macromolecules, which attain in vivo activity via antigen delivery and immunostimulation mechanisms. Over the last decades, the technology has witnessed evolvement of next generation members, expansion to include various antigens and routes of administration, and progression to clinical phase. This was accompanied by gaining important insights into the mechanism of action and the development of a novel class of virus-mimicking nano-assemblies for antigen delivery. The present review evaluates in vitro and in vivo data generated to date in the context of latest advances in understanding the primary function and biophysical behavior of these macromolecules. It also provides an overview of relevant synthetic and characterization methods, macromolecular biodegradation pathways, and polyphosphazene-based multicomponent, nanoparticulate, and microfabricated formulations.
引用
收藏
页码:299 / 315
页数:17
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