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两组分蛋白纳米颗粒疫苗的设计与免疫评价用于东非昏睡病。

Design and immunological evaluation of two-component protein nanoparticle vaccines for East Coast fever.

机构信息

Animal and Human Health program, International Livestock Research Institute (ILRI), Nairobi, Kenya.

Department of Biochemistry, University of Washington, Seattle, WA, United States.

出版信息

Front Immunol. 2023 Jan 13;13:1015840. doi: 10.3389/fimmu.2022.1015840. eCollection 2022.

DOI:10.3389/fimmu.2022.1015840
PMID:36713406
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9880323/
Abstract

Nanoparticle vaccines usually prime stronger immune responses than soluble antigens. Within this class of subunit vaccines, the recent development of computationally designed self-assembling two-component protein nanoparticle scaffolds provides a powerful and versatile platform for displaying multiple copies of one or more antigens. Here we report the generation of three different nanoparticle immunogens displaying 60 copies of p67C, an 80 amino acid polypeptide from a candidate vaccine antigen of , and their immunogenicity in cattle. p67C is a truncation of p67, the major surface protein of the sporozoite stage of , an apicomplexan parasite that causes an often-fatal bovine disease called East Coast fever (ECF) in sub-Saharan Africa. Compared to I32-19 and I32-28, we found that I53-50 nanoparticle scaffolds displaying p67C had the best biophysical characteristics. p67C-I53-50 also outperformed the other two nanoparticles in stimulating p67C-specific IgG1 and IgG2 antibodies and CD4 T-cell responses, as well as sporozoite neutralizing capacity. In experimental cattle vaccine trials, p67C-I53-50 induced significant immunity to ECF, suggesting that the I53-50 scaffold is a promising candidate for developing novel nanoparticle vaccines. To our knowledge this is the first application of computationally designed nanoparticles to the development of livestock vaccines.

摘要

纳米颗粒疫苗通常比可溶性抗原引发更强的免疫反应。在亚单位疫苗这一类中,最近开发的计算设计的自组装两亲性蛋白质纳米颗粒支架为展示一个或多个抗原的多个拷贝提供了强大而通用的平台。在这里,我们报告了三种不同的纳米颗粒免疫原的产生,这些免疫原展示了 60 个拷贝的 p67C,p67C 是候选疫苗抗原 p67 的 80 个氨基酸多肽,以及它们在牛中的免疫原性。p67C 是 p67 的截断物,p67 是引起东非裂谷热(ECF)的顶复门寄生虫疟原虫的子孢子阶段的主要表面蛋白。与 I32-19 和 I32-28 相比,我们发现展示 p67C 的 I53-50 纳米颗粒支架具有最佳的物理特性。p67C-I53-50 在刺激 p67C 特异性 IgG1 和 IgG2 抗体和 CD4 T 细胞反应以及子孢子中和能力方面也优于其他两种纳米颗粒。在实验牛疫苗试验中,p67C-I53-50 诱导了对 ECF 的显著免疫,表明 I53-50 支架是开发新型纳米颗粒疫苗的有前途的候选物。据我们所知,这是首次将计算设计的纳米颗粒应用于家畜疫苗的开发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9073/9880323/37989b1bdac6/fimmu-13-1015840-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9073/9880323/f290c2dca9d4/fimmu-13-1015840-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9073/9880323/ff2cf245d486/fimmu-13-1015840-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9073/9880323/17d3e28554ab/fimmu-13-1015840-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9073/9880323/b6efd442f248/fimmu-13-1015840-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9073/9880323/c345834d3c34/fimmu-13-1015840-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9073/9880323/c0e10cf182f6/fimmu-13-1015840-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9073/9880323/6d0663f5880e/fimmu-13-1015840-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9073/9880323/25e83e205b20/fimmu-13-1015840-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9073/9880323/37989b1bdac6/fimmu-13-1015840-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9073/9880323/f290c2dca9d4/fimmu-13-1015840-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9073/9880323/ff2cf245d486/fimmu-13-1015840-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9073/9880323/17d3e28554ab/fimmu-13-1015840-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9073/9880323/b6efd442f248/fimmu-13-1015840-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9073/9880323/c345834d3c34/fimmu-13-1015840-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9073/9880323/c0e10cf182f6/fimmu-13-1015840-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9073/9880323/6d0663f5880e/fimmu-13-1015840-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9073/9880323/25e83e205b20/fimmu-13-1015840-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9073/9880323/37989b1bdac6/fimmu-13-1015840-g009.jpg

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