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

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.

Keywords: African swine fever; control disease; cross-protection; vaccine; virus; wild boar.

MeSH terms

  • Administration, Oral
  • African Swine Fever Virus* / immunology
  • African Swine Fever* / immunology
  • African Swine Fever* / prevention & control
  • African Swine Fever* / virology
  • Animals
  • Cross Protection* / immunology
  • Sus scrofa*
  • Swine
  • Vaccination*
  • Vaccine Development
  • Vaccines, Attenuated* / immunology
  • Viral Vaccines* / administration & dosage
  • Viral Vaccines* / immunology

Substances

  • Viral Vaccines
  • Vaccines, Attenuated

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This research was funded by the H2020 VACDIVA 862874 project. JB is a recipient of a “Ramón y Cajal” contract (RYC2022-038060-I) funded by the Spanish Ministry of Science and Innovation (MCIN/AEI) and Fondo Social Europeo Plus (FSE+).