Intravaginal Zinc Oxide Tetrapod Nanoparticles as Novel Immunoprotective Agents against Genital Herpes

被引:110
作者
Antoine, Thessicar E. [1 ,2 ]
Hadigal, Satvik R. [1 ]
Yakoub, Abraam M. [1 ,2 ]
Mishra, Yogendra Kumar [3 ]
Bhattacharya, Palash [2 ]
Haddad, Christine [2 ]
Valyi-Nagy, Tibor [4 ]
Adelung, Rainer [3 ]
Prabhakar, Bellur S. [2 ]
Shukla, Deepak [1 ,2 ]
机构
[1] Univ Illinois, Dept Ophthalmol & Visual Sci, 1855 West Taylor St, Chicago, IL 60612 USA
[2] Univ Illinois, Dept Microbiol & Immunol, Chicago, IL 60612 USA
[3] Univ Kiel, Inst Mat Sci, D-24143 Kiel, Germany
[4] Univ Illinois, Dept Pathol, Chicago, IL 60612 USA
基金
美国国家卫生研究院;
关键词
SIMPLEX-VIRUS TYPE-2; CD8(+) T-CELLS; GLYCOPROTEIN VACCINE; VAGINAL INFECTION; MOUSE; RECOGNITION; RECEPTORS; NETWORKS; PROTEINS; INSIGHTS;
D O I
10.4049/jimmunol.1502373
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Virtually all efforts to generate an effective protection against the life-long, recurrent genital infections caused by HSV-2 have failed. Apart from sexual transmission, the virus can also be transmitted from mothers to neonates, and it is a key facilitator of HIV coacquisition. In this article, we uncover a nanoimmunotherapy using specially designed zinc oxide tetrapod nanoparticles (ZOTEN) with engineered oxygen vacancies. We demonstrate that ZOTEN, when used intravaginally as a microbicide, is an effective suppressor of HSV-2 genital infection in female BALB/c mice. The strong HSV-2 trapping ability of ZOTEN significantly reduced the clinical signs of vaginal infection and effectively decreased animal mortality. In parallel, ZOTEN promoted the presentation of bound HSV-2 virions to mucosal APCs, enhancing T cell-mediated and Ab-mediated responses to the infection, and thereby suppressing a reinfection. We also found that ZOTEN exhibits strong adjuvant-like properties, which is highly comparable with alum, a commonly used adjuvant. Overall, to our knowledge, our study provides the very first evidence for the protective efficacy of an intravaginal microbicide/vaccine or microbivac platform against primary and secondary female genital herpes infections.
引用
收藏
页码:4566 / 4575
页数:10
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