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挑战边界:非洲猪瘟疫苗开发是否需要进行交叉保护评估?野猪口服疫苗接种的案例。

Challenging boundaries: is cross-protection evaluation necessary for African swine fever vaccine development? A case of oral vaccination in wild boar.

机构信息

VISAVET Health Surveillance Center, Complutense University of Madrid, Madrid, Spain.

Department of Animal Health, Faculty of Veterinary, Complutense University of Madrid, Madrid, Spain.

出版信息

Front Immunol. 2024 Oct 1;15:1388812. doi: 10.3389/fimmu.2024.1388812. eCollection 2024.

Abstract

African swine fever (ASF) poses a significant threat to domestic pigs and wild boar (Sus scrofa) populations, with the current epidemiological situation more critical than ever. The disease has spread across five continents, causing devastating losses in the swine industry. Although extensive research efforts are ongoing to develop an effective and safe vaccine, this goal remains difficult to achieve. Among the potential vaccine candidates, live attenuated viruses (LAVs) have emerged as the most promising option due to their ability to provide strong protection against experimental challenges. However, ASF virus (ASFV) is highly diverse, with genetic and phenotypic variations across different isolates, which differ in virulence. This study highlights the limitations of a natural LAV strain (Lv17/WB/Rie1), which showed partial efficacy against a highly virulent and partially heterologous isolate (Arm07; genotype II). However, the LAV's effectiveness was incomplete when tested against a more phylogenetically distant virus (Ken06.Bus; genotype IX). These findings raise concerns about the feasibility of developing a universal vaccine for ASFV in the near future, emphasizing the urgent need to assess the protective scope of LAV candidates across different ASFV isolates to better define their limitations.

摘要

非洲猪瘟(ASF)对家猪和野猪(Sus scrofa)种群构成重大威胁,目前的流行病学形势比以往任何时候都更加严峻。该疾病已蔓延至五大洲,给养猪业造成了毁灭性的损失。尽管正在进行广泛的研究努力来开发有效和安全的疫苗,但这一目标仍然难以实现。在潜在的疫苗候选物中,活减毒病毒(LAV)由于能够提供针对实验挑战的强大保护而成为最有前途的选择。然而,ASF 病毒(ASFV)高度多样化,不同分离株之间存在遗传和表型变异,其毒力也有所不同。本研究强调了天然 LAV 株(Lv17/WB/Rie1)的局限性,该株对高度毒力和部分异源分离株(Arm07;基因型 II)具有部分疗效。然而,当该 LAV 株用于对抗亲缘关系更远的病毒(Ken06.Bus;基因型 IX)时,其效果并不完全。这些发现令人担忧,在不久的将来是否能够开发出针对 ASFV 的通用疫苗,这强调了迫切需要评估不同 ASFV 分离株的 LAV 候选物的保护范围,以更好地定义其局限性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d58a/11473374/0a7fa145a783/fimmu-15-1388812-g001.jpg

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