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Virus-Like Particle, Liposome, and Polymeric Particle-Based Vaccines against HIV-1
被引:47
|作者:
Gao, Yong
[1
]
Wijewardhana, Chanuka
[1
]
Mann, Jamie F. S.
[1
]
机构:
[1] Univ Western Ontario, Dept Microbiol & Immunol, London, ON, Canada
来源:
关键词:
HIV-1;
vaccine;
virus-like particles;
nanoparticles;
immunogenicity;
HUMAN-PAPILLOMAVIRUS TYPE-16;
NEUTRALIZING ANTIBODY-RESPONSES;
GERMINAL CENTER RESPONSES;
MONOPHOSPHORYL-LIPID-A;
IMMUNE-RESPONSE;
SKELETAL-MUSCLE;
CELLULAR-IMMUNITY;
VESICLE SIZE;
DOUBLE-BLIND;
SUBUNIT VACCINE;
D O I:
10.3389/fimmu.2018.00345
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
It is acknowledged that vaccines remain the best hope for eliminating the HIV-1 epidemic. However, the failure to produce effective vaccine immunogens and the inability of conventional delivery strategies to elicit the desired immune responses remains a central theme and has ultimately led to a significant roadblock in HIV vaccine development. Consequently, significant efforts have been applied to generate novel vaccine antigens and delivery agents, which mimic viral structures for optimal immune induction. Here, we review the latest developments that have occurred in the nanoparticle vaccine field, with special emphasis on strategies that are being utilized to attain highly immunogenic, systemic, and mucosal anti-HIV humoral and cellular immune responses. This includes the design of novel immunogens, the central role of antigen-presenting cells, delivery routes, and biodistribution of nanoparticles to lymph nodes. In particular, we will focus on virus-like-particle formulations and their preclinical uses within the HIV prophylactic vaccine setting.
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