Negatively Charged Liposomes Show Potent Adjuvant Activity When Simply Admixed with Protein Antigens

被引:37
作者
Yanasarn, Nijaporn [1 ,2 ]
Sloat, Brian R. [1 ]
Cui, Zhengrong [1 ]
机构
[1] Univ Texas Austin, Coll Pharm, Div Pharmaceut, Austin, TX 78712 USA
[2] Oregon State Univ, Coll Pharm, Dept Pharmaceut Sci, Corvallis, OR 97331 USA
基金
美国国家卫生研究院;
关键词
protein antigen; antibody response; CTL; antitumor activity; antigen uptake; APC activation; IMMUNE-RESPONSE; PROTECTIVE IMMUNITY; CATIONIC LIPOSOME; GENE-EXPRESSION; DENDRITIC CELLS; BALB/C MICE; VACCINE; SURFACE; INDUCTION; IMMUNOADJUVANT;
D O I
10.1021/mp200016d
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Liposomes have been investigated extensively as a vaccine delivery system. Herein the adjuvant activities of liposomes with different net surface charges (neutral, positive, or negative) were evaluated when admixed with protein antigens, ovalbumin (OVA, pI = 4.7), Bacillus anthracis, protective antigen protein (PA, pI = 5.6), or cationized OVA (cOVA). Mice immunized subcutaneously with OVA admixed with different liposomes generated different antibody responses. Interestingly, OVA admixed with net negatively charged liposomes prepared with DOPA was as immunogenic as OVA admixed with positively charged liposomes prepared with DOTAP. Immunization of mice with the anthrax PA protein admixed with the net negatively charged DOPA liposomes also induced a strong and functional anti-PA antibody response. When the cationized OVA was used as a model antigen, liposomes with net neutral, negative, or positive charges showed comparable adjuvant activities. Immunization of mice with the OVA admixed with DOPA liposomes also induced OVA-specific CD8(+) cytotoxic T lymphocyte responses and significantly delayed the growth of OVA-expressing B16-OVA tumors in mice. However, not all net negatively charged liposomes showed a strong adjuvant activity. The adjuvant activity of the negatively charged liposomes may be related to the liposome's ability (i) to upregulate the expression of molecules related to the activation and maturation of antigen-presenting cells and (ii) to slightly facilitate the uptake of the antigens by antigen-presenting cells. Simply admixing certain negatively charged liposomes with certain protein antigens of interest may represent a novel platform for vaccine development.
引用
收藏
页码:1174 / 1185
页数:12
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