Immunostimulatory DNA is a potent mucosal adjuvant

被引:84
作者
Horner, AA
Ronaghy, A
Cheng, PM
Nguyen, MD
Cho, HJ
Broide, D
Raz, E
机构
[1] Univ Calif San Diego, Sam & Rose Stein Inst Aging, Dept Med, La Jolla, CA 92093 USA
[2] Dynavax Technol Corp, San Diego, CA 92121 USA
关键词
immunostimulatory sequence DNA; mucosal; adjuvant; IgA; vaccination;
D O I
10.1006/cimm.1998.1400
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Most proteins delivered to mucosal surfaces fail to induce mucosal or systemic immune responses. Ne demonstrate that a single intranasal (i.n.) coadministration of a model antigen (beta-galactosidase, beta-gal) with immunostimulatory sequence oligodeoxynucleotide (ISS-ODN) induces a mucosal IgA response equivalent to that induced by i.n. codelivery of beta-gal with cholera toxin (CT). Furthermore, i.n. and intradermal (i.d.) delivery of the beta-gal/ISS-ODN mix stimulates equivalent Th-1-biased systemic immune responses with high-level cytotoxic T lymphocyte (CTL) activity. In contrast, i.n. immunization with beta-gal and CT results in a Th-1-biased systemic immune response with poor CTL activity. Our data show that i.n. delivery of ISS-ODN provides effective adjuvant activity for the induction of both mucosal and systemic Th-1-biased immune responses. This immunization approach deserves consideration in the development of vaccines against mucosal pathogens. (C) 1998 Academic Press.
引用
收藏
页码:77 / 82
页数:6
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