Polyethyleneimine is a potent mucosal adjuvant for viral glycoprotein antigens

被引:185
作者
Wegmann, Frank [1 ]
Gartlan, Kate H. [1 ]
Harandi, Ali M. [2 ]
Brinckmann, Sarah A. [1 ]
Coccia, Margherita [1 ]
Hillson, William R. [1 ]
Kok, Wai Ling [3 ]
Cole, Suzanne [3 ]
Ho, Ling-Pei [3 ]
Lambe, Teresa [4 ]
Puthia, Manoj [5 ]
Svanborg, Catharina [5 ]
Scherer, Erin M. [6 ]
Krashias, George [1 ]
Williams, Adam [7 ]
Blattman, Joseph N. [6 ]
Greenberg, Philip D. [6 ]
Flavell, Richard A. [7 ]
Moghaddam, Amin E. [1 ]
Sheppard, Neil C. [1 ]
Sattentau, Quentin J. [1 ]
机构
[1] Univ Oxford, Sir William Dunn Sch Pathol, Oxford OX1 3RE, England
[2] Univ Gothenburg, Sahlgrenska Acad, Inst Biomed, Dept Microbiol & Immunol, Gothenburg, Sweden
[3] John Radcliffe Hosp, MRC, Human Immunol Unit, Weatherall Inst Mol Med, Oxford OX3 9DU, England
[4] Univ Oxford, Jenner Inst, Oxford, England
[5] Lund Univ, Div Microbiol Immunol & Glycobiol, Lund, Sweden
[6] Univ Washington, Dept Immunol, Seattle, WA 98195 USA
[7] Yale Univ, Sch Med, New Haven, CT USA
关键词
INTRANASAL DELIVERY; PROTECTIVE IMMUNITY; ANTIBODY-RESPONSES; NALP3; INFLAMMASOME; DENDRITIC CELLS; GENE DELIVERY; BELLS-PALSY; VACCINE; INNATE; MUTANT;
D O I
10.1038/nbt.2344
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
Protection against mucosally transmitted infections probably requires immunity at the site of pathogen entry(1), yet there are no mucosal adjuvant formulations licensed for human use. Polyethyleneimine (PEI) represents a family of organic polycations used as nucleic acid transfection reagents in vitro and DNA vaccine delivery vehicles in vivo(2,3). Here we show that diverse PEI forms have potent mucosal adjuvant activity for viral subunit glycoprotein antigens. A single intranasal administration of influenza hemagglutinin or herpes simplex virus type-2 (HSV-2) glycoprotein D with PEI elicited robust antibody-mediated protection from an otherwise lethal infection, and was superior to existing experimental mucosal adjuvants. PEI formed nanoscale complexes with antigen, which were taken up by antigen-presenting cells in vitro and in vivo, promoted dendritic cell trafficking to draining lymph nodes and induced non-proinflammatory cytokine responses. PEI adjuvanticity required release of host double-stranded DNA that triggered Irf3-dependent signaling. PEI therefore merits further investigation as a mucosal adjuvant for human use.
引用
收藏
页码:883 / U116
页数:8
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