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基于伪狂犬病病毒糖蛋白 D 的自组装纳米颗粒疫苗诱导针对伪狂犬病病毒感染的强烈保护免疫。

A self-assembled nanoparticle vaccine based on pseudorabies virus glycoprotein D induces potent protective immunity against pseudorabies virus infection.

机构信息

National Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan 430070, Hubei, China; College of Veterinary Medicine, Huazhong Agricultural University, Wuhan 430070, Hubei, China.

National Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan 430070, Hubei, China; College of Veterinary Medicine, Huazhong Agricultural University, Wuhan 430070, Hubei, China; The Cooperative Innovation Center for Sustainable Pig Production, Wuhan 430070, Hubei, China.

出版信息

Vet Microbiol. 2023 Sep;284:109799. doi: 10.1016/j.vetmic.2023.109799. Epub 2023 Jun 5.

Abstract

Pseudorabies virus (PRV) mainly causes pseudorabies (PR) or Aujeszky's disease in pigs and can infect humans, raising public health concerns about zoonotic and interspecies transmission of PR. With the emergence of PRV variants in 2011, the classic attenuated PRV vaccine strains have failed to protect many swine herds against PR. Herein, we developed a self-assembled nanoparticle vaccine that induces potent protective immunity against PRV infection. PRV glycoprotein D (gD) was expressed using the baculovirus expression system and further presented on the lumazine synthase (LS) 60-meric protein scaffolds via the SpyTag003/SpyCatcher003 covalent coupling system. In mouse and piglet models, LSgD nanoparticles emulsified with the ISA 201VG adjuvant elicited robust humoral and cellular immune responses. Furthermore, LSgD nanoparticles provided effective protection against PRV infection and eliminated pathological symptoms in the brain and lungs. Collectively, the gD-based nanoparticle vaccine design appears to be a promising candidate for potent protection against PRV infection.

摘要

伪狂犬病病毒(PRV)主要引起猪的伪狂犬病(PR)或奥耶斯基氏病,可感染人类,引起人们对 PR 的人畜共患病和种间传播的公共卫生关注。自 2011 年 PRV 变异株出现以来,经典的减毒 PRV 疫苗株未能保护许多猪群免受 PR 的侵害。在此,我们开发了一种自组装的纳米颗粒疫苗,可诱导针对 PRV 感染的强大保护性免疫。使用杆状病毒表达系统表达 PRV 糖蛋白 D(gD),并通过 SpyTag003/SpyCatcher003 共价偶联系统进一步在荧光素酶(LS)60 聚体蛋白支架上呈现。在小鼠和仔猪模型中,与 ISA 201VG 佐剂乳化的 LSgD 纳米颗粒引发了强大的体液和细胞免疫反应。此外,LSgD 纳米颗粒提供了针对 PRV 感染的有效保护,并消除了大脑和肺部的病理症状。总之,基于 gD 的纳米颗粒疫苗设计似乎是预防 PRV 感染的有前途的候选物。

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