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

被引:0
|
作者
Cadenas-Fernandez, Estefania [1 ,2 ]
Barroso-Arevalo, Sandra [1 ,2 ]
Kosowska, Aleksandra [1 ,2 ]
Diaz-Frutos, Marta [1 ,2 ]
Gallardo, Carmina [3 ]
Rodriguez-Bertos, Antonio [1 ,4 ]
Bosch, Jaime [1 ,2 ]
Sanchez-Vizcaino, Jose M. [1 ,2 ]
Barasona, Jose A. [1 ,2 ]
机构
[1] Univ Complutense Madrid, VISAVET Hlth Surveillance Ctr, Madrid, Spain
[2] Univ Complutense Madrid, Fac Vet, Dept Anim Hlth, Madrid, Spain
[3] Ctr Invest Sanidad Anim CISA INIA CSIC, European Union Reference Lab African Swine Fever A, Valdeolmos, Spain
[4] Univ Complutense Madrid, Fac Vet, Dept Internal Med & Anim Surg, Madrid, Spain
来源
FRONTIERS IN IMMUNOLOGY | 2024年 / 15卷
基金
欧盟地平线“2020”;
关键词
African swine fever; control disease; cross-protection; virus; vaccine; wild boar; ISOLATE HARBORING DELETIONS; VIRUS; GEORGIA; GENES;
D O I
10.3389/fimmu.2024.1388812
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
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页数:12
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