Live-vectored antigen cocktail confers protection against African swine fever virus (ASFV) Georgia 2007/1 challenge

Live-vectored antigen cocktail confers protection against African swine fever virus (ASFV) Georgia 2007/1 challenge

  • Zhu, G. et al. Structural basis of RNA polymerase complexes in African swine fever virus. Nat. Commun. 16, 501 (2025).


    Google Scholar
     

  • Spinard, E. et al. A re-evaluation of African swine fever genotypes based on p72 sequences reveals the existence of only six distinct p72 groups. Viruses 15, 2246 (2023).


    Google Scholar
     

  • Njau, E. P. et al. The first genotype II African swine fever virus isolated in Africa provides insight into the current Eurasian pandemic. Sci. Rep. 11, 13081 (2021).


    Google Scholar
     

  • Coelho, I. M. P., Paiva, M. T., Da Costa, A. J. A. & Nicolino, R. R. African Swine Fever: Spread and seasonal patterns worldwide. Prev. Vet. Med. 235, 106401 (2025).


    Google Scholar
     

  • OIE. African Swine Fever (ASF)—Situation Reports https://www.woah.org/en/disease/african-swine-fever/ (2025).

  • Dixon, L. K. Advances in African swine fever virus molecular biology and host interactions contributing to new tools for control. J. Virol. 99, e00932–00924 (2025).


    Google Scholar
     

  • Ruedas-Torres, I., Thi To Nga, B. & Salguero, F. J. Pathogenicity and virulence of African swine fever virus. Virulence 15, 2375550 (2024).


    Google Scholar
     

  • Guinat, C. et al. Transmission routes of African swine fever virus to domestic pigs: current knowledge and future research directions. Vet. Rec. 178, 262–267 (2016).


    Google Scholar
     

  • Montgomery, R. E. On a form of swine fever occurring in British East Africa (Kenya Colony). J. Comp. Pathol. 34, 242 (1921).


    Google Scholar
     

  • de Carvalho Ferreira, H. C. et al. African swine fever virus excretion patterns in persistently infected animals: a quantitative approach. Vet. Microbiol. 160, 327–340 (2012).


    Google Scholar
     

  • Chandana, M. S. et al. Recent progress and major gaps in the vaccine development for African swine fever. Braz. J. Microbiol. 55, 997–1010 (2024).


    Google Scholar
     

  • Montgomery, R. E. Immunization with Attenuated Virus—Annual Reports of the Chief Veterinary Research Officer, Agricultural Department, Kenya (Agricultural Department,1921–1927).

  • Sanford, B. et al. Deletion of the thymidine kinase gene induces complete attenuation of the Georgia isolate of African swine fever virus. Virus Res. 213, 165–171 (2016).


    Google Scholar
     

  • Sang, H. et al. Progress toward development of effective and safe African swine fever virus vaccines. Front. Vet. Sci. 7, 84 (2020).


    Google Scholar
     

  • Rock, D. L. Thoughts on African swine fever vaccines. Viruses 13, 943 (2021).


    Google Scholar
     

  • Diep, N. V. et al. Genotype II live-attenuated ASFV vaccine strains unable to completely protect pigs against the emerging recombinant ASFV genotype I/II strain in Vietnam. Vaccines (Basel) 12, 1114 (2024).


    Google Scholar
     

  • Nefedeva, M., Titov, I., Tsybanov, S. & Malogolovkin, A. Recombination shapes African swine fever virus serotype-specific locus evolution. Sci. Rep. 10, 18474 (2020).


    Google Scholar
     

  • Zhao, D. et al. Highly lethal genotype I and II recombinant African swine fever viruses detected in pigs. Nat. Commun. 14, 3096 (2023).


    Google Scholar
     

  • van den Born, E. et al. African swine fever virus vaccine strain Asfv-G-∆ I177l reverts to virulence and negatively affects reproductive performance. npj Vaccines 10, 46 (2025).


    Google Scholar
     

  • Zhang, Y. et al. ASFV subunit vaccines: strategies and prospects for future development. Microb. Pathog. 197, 107063 (2024).


    Google Scholar
     

  • Escribano, J. M., Galindo, I. & Alonso, C. Antibody-mediated neutralization of African swine fever virus: myths and facts. Virus Res. 173, 101–109 (2013).


    Google Scholar
     

  • Yang, X. et al. The antibodies against the A137R protein drive antibody-dependent enhancement of African swine fever virus infection in porcine alveolar macrophages. Emerg. Microbes Infect. 13, 2377599 (2024).


    Google Scholar
     

  • Sunwoo, S. Y. et al. DNA–protein vaccination strategy does not protect from challenge with African swine fever virus Armenia 2007 strain. Vaccines (Basel) 7, 12 (2019).


    Google Scholar
     

  • Schafer, A. et al. Adaptive cellular immunity against African swine fever virus infections. Pathogens 11, 274 (2022).


    Google Scholar
     

  • Takamatsu, H. H. et al. Cellular immunity in ASFV responses. Virus Res. 173, 110–121 (2013).


    Google Scholar
     

  • Oura, C. A. L., Denyer, M. S., Takamatsu, H. & Parkhouse, R. M. E. In vivo depletion of CD8+ T lymphocytes abrogates protective immunity to African swine fever virus. J. Gen. Virol. 86, 2445–2450 (2005).


    Google Scholar
     

  • Lokhandwala, S. et al. Adenovirus-vectored African swine fever virus antigen cocktails are immunogenic but not protective against intranasal challenge with Georgia 2007/1 isolate. Vet. Microbiol. 235, 10–20 (2019).


    Google Scholar
     

  • Zajac, M. D. et al. Immunization of pigs with replication-incompetent adenovirus-vectored African swine fever virus multi-antigens induced humoral immune responses but no protection following contact challenge. Front. Vet. Sci. 10, 1208275 (2023).


    Google Scholar
     

  • Portugal, R. et al. Six adenoviral vectored African swine fever virus genes protect against fatal disease caused by genotype I challenge. J. Virol. 98, e0062224 (2024).


    Google Scholar
     

  • Goatley, L. C. et al. A pool of eight virally vectored African swine fever antigens protect pigs against fatal disease. Vaccines (Basel) 8, 234 (2020).


    Google Scholar
     

  • Peng, B. et al. Replicating rather than nonreplicating adenovirus–human immunodeficiency virus recombinant vaccines are better at eliciting potent cellular immunity and priming high-titer antibodies. J. Virol. 79, 10200–10209 (2005).


    Google Scholar
     

  • Li, Y. et al. Immunization with recombinant Sao protein confers protection against Streptococcus suis infection. Clin. Vaccin. Immunol. 14, 937–943 (2007).


    Google Scholar
     

  • Singh, M. & O’Hagan, D. T. Recent advances in veterinary vaccine adjuvants. Int. J. Parasitol. 33, 469–478 (2003).


    Google Scholar
     

  • Trapani, J. A. Granzymes: a family of lymphocyte granule serine proteases. Genome Biol. 2, Reviews3014 (2001).


    Google Scholar
     

  • Jawalagatti, V., Kirthika, P., Park, J. Y., Hewawaduge, C. & Lee, J. H. Highly feasible immunoprotective multicistronic SARS-CoV-2 vaccine candidate blending novel eukaryotic expression and Salmonella bactofection. J. Adv. Res. 36, 211–222 (2022).


    Google Scholar
     

  • Kim, J. H. et al. High cleavage efficiency of a 2A peptide derived from porcine teschovirus-1 in human cell lines, zebrafish and mice. PLoS ONE 6, e18556 (2011).


    Google Scholar
     

  • Alexander, J. et al. Pre-clinical evaluation of a replication-competent recombinant adenovirus serotype 4 vaccine expressing influenza H5 hemagglutinin. PLoS ONE 7, e31177 (2012).


    Google Scholar
     

  • Elkashif, A., Alhashimi, M., Sayedahmed, E. E., Sambhara, S. & Mittal, S. K. Adenoviral vector-based platforms for developing effective vaccines to combat respiratory viral infections. Clin. Transl. Immunol. 10, e1345 (2021).


    Google Scholar
     

  • Mudrick, H. E. et al. Comparison of replicating and nonreplicating vaccines against SARS-CoV-2. Sci. Adv. 8, eabm8563 (2022).


    Google Scholar
     

  • Shaimardanova, A. A. et al. Production and application of multicistronic constructs for various human disease therapies. Pharmaceutics 11, https://doi.org/10.3390/pharmaceutics11110580 (2019).

  • Blome, S., Gabriel, C. & Beer, M. Modern adjuvants do not enhance the efficacy of an inactivated African swine fever virus vaccine preparation. Vaccine 32, 3879–3882 (2014).


    Google Scholar
     

  • Howey, E. B., O’Donnell, V., de Carvalho Ferreira, H. C., Borca, M. V. & Arzt, J. Pathogenesis of highly virulent African swine fever virus in domestic pigs exposed via intraoropharyngeal, intranasopharyngeal, and intramuscular inoculation, and by direct contact with infected pigs. Virus Res 178, 328–339 (2013).


    Google Scholar
     

  • Guinat, C. et al. Dynamics of African swine fever virus shedding and excretion in domestic pigs infected by intramuscular inoculation and contact transmission. Vet. Res. 45, 93 (2014).


    Google Scholar
     

  • Bosch-Camós, L. et al. Cross-protection against African swine fever virus upon intranasal vaccination is associated with an adaptive-innate immune crosstalk. PLoS Pathog. 18, e1010931 (2022).


    Google Scholar
     

  • Arias, M. et al. Approaches and perspectives for development of African swine fever virus. Vaccines 5, 35 (2017).


    Google Scholar
     

  • Bosch-Camós, L., López, E. & Rodriguez, F. African swine fever vaccines: a promising work still in progress. Porcine Health Manag. 6, 17 (2020).


    Google Scholar
     

  • Neilan, J. G. et al. Neutralizing antibodies to African swine fever virus proteins p30, p54, and p72 are not sufficient for antibody-mediated protection. Virology 319, 337–342 (2004).


    Google Scholar
     

  • Salguero, F. J. Comparative pathology and pathogenesis of African swine fever infection in swine. Front. Vet. Sci. 7, 282 (2020).


    Google Scholar
     

  • Galindo-Cardiel, I. et al. Standardization of pathological investigations in the framework of experimental ASFV infections. Virus Res. 173, 180–190 (2013).


    Google Scholar
     

  • Lokhandwala, S. et al. Induction of robust immune responses in swine by using a cocktail of adenovirus-vectored African swine fever virus antigens. Clin. Vaccin. Immunol. 23, 888–900 (2016).


    Google Scholar
     

  • Friedrichs, V., Streitz, M., Beer, M., Blome, S. & Schäfer, A. Maternal immunity and African swine fever virus: understanding the limits of passive protection. Front. Immunol. 16, 1593820 (2025).


    Google Scholar
     

  • Schlafer, D. H., Mcvicar, J. W. & Mebus, C. A. African swine fever convalescent sows—subsequent pregnancy and the effect of colostral antibody on challenge inoculation of their pigs. Am. J. Vet. Res. 45, 1361–1366 (1984).


    Google Scholar
     

  • Onisk, D. V. et al. Passively transferred African swine fever virus antibodies protect swine against lethal infection. Virology 198, 350–354 (1994).


    Google Scholar
     

  • Wardley, R. C., Norley, S. G., Wilkinson, P. J. & Williams, S. The role of antibody in protection against African swine fever virus. Vet. Immunol. Immunopathol. 9, 201–212 (1985).


    Google Scholar
     

  • Attreed, S. E. et al. A highly effective African swine fever virus vaccine elicits a memory T cell response in vaccinated swine. Pathogens 11, 1438 (2022).


    Google Scholar
     

  • Zajac, M. D. et al. Adenovirus-vectored African swine fever virus pp220 induces robust antibody, IFN-gamma, and CTL responses in pigs. Front. Vet. Sci. 9, 921481 (2022).


    Google Scholar
     

  • Vanselow, B. A., Abetz, I. & Trenfield, K. A bovine ephemeral fever vaccine incorporating adjuvant Quil A: a comparative study using adjuvants Quil A, aluminium hydroxide gel and dextran sulphate. Vet. Rec. 117, 37–43 (1985).


    Google Scholar
     

  • Crawley, A., Raymond, C. & Wilkie, B. N. Control of immunoglobulin isotype production by porcine B-cells cultured with cytokines. Vet. Immunol. Immunopathol. 91, 141–154 (2003).


    Google Scholar
     

  • Crawley, A. & Wilkie, B. N. Porcine Ig isotypes: function and molecular characteristics. Vaccine 21, 2911–2922 (2003).


    Google Scholar
     

  • Liu, W. et al. A new vaccination regimen using adenovirus-vectored vaccine confers effective protection against African swine fever virus in swine. Emerg. Microbes Infect. 12, 2233643 (2023).


    Google Scholar
     

  • Lokhandwala, S. et al. Adenovirus-vectored novel African Swine Fever Virus antigens elicit robust immune responses in swine. PLoS ONE 12, e0177007 (2017).


    Google Scholar
     

  • Su, Q., Sena-Esteves, M. & Gao, G. Purification of the recombinant adenovirus by cesium chloride gradient centrifugation. Cold Spring Harb. Protoc. 2019, (2019). https://doi.org/10.1101/pdb.prot095547.

  • Singleton, H., Graham, S. P., Bodman-Smith, K. B., Frossard, J.-P. & Steinbach, F. Establishing porcine monocyte-derived macrophage and dendritic cell systems for studying the interaction with PRRSV-1. Front. Microbiol. 7, https://doi.org/10.3389/fmicb.2016.00832 (2016).

  • Goatley, L. C., Nash, R. & Netherton, C. L. Primary macrophage culture from porcine blood and lungs. Methods Mol. Biol. 2503, 63–72 (2022).


    Google Scholar
     

  • Ho, C. S. et al. Nomenclature for factors of the SLA system, update 2008. Tissue Antigens 73, 307–315 (2009).


    Google Scholar
     

  • Hammer, S. E. et al. Importance of the major histocompatibility complex (swine leukocyte antigen) in swine health and biomedical research. Annu Rev. Anim. Biosci. 8, 171–198 (2020).


    Google Scholar
     

  • Ho, C. S. et al. Molecular characterization of swine leucocyte antigen class I genes in outbred pig populations. Anim. Genet. 40, 468–478 (2009).


    Google Scholar
     

  • Ho, C. S. et al. Molecular characterization of swine leucocyte antigen class II genes in outbred pig populations. Anim. Genet. 41, 428–432 (2010).


    Google Scholar
     

  • Gao, C. et al. Swine leukocyte antigen diversity in Canadian specific pathogen-free Yorkshire and Landrace pigs. Front. Immunol. 8, 282 (2017).


    Google Scholar
     

  • Hammer, S. E. et al. Comparative analysis of swine leukocyte antigen gene diversity in European farmed pigs. Anim. Genet. 52, 523–531 (2021).


    Google Scholar
     

  • Techakriengkrai, N., Nedumpun, T., Golde, W. T. & Suradhat, S. Diversity of the swine leukocyte antigen Class I and II in commercial pig populations. Front. Vet. Sci. 8, 637682 (2021).


    Google Scholar
     

  • Hammer, S. E. et al. in 6th European Veterinary and Immunology Workshop (EVIW) (ed. Rutten, V.) The European Veterinary Immunology Group (EVIG).

  • Sørensen, M. R. et al. Sequence-based genotyping of expressed swine leukocyte antigen Class I alleles by next-generation sequencing reveal novel swine leukocyte antigen Class I haplotypes and alleles in Belgian, Danish, and Kenyan fattening pigs and Göttingen Minipigs. Front. Immunol. 8, https://doi.org/10.3389/fimmu.2017.00701 (2017).

  • Luetkemeier, E. S., Malhi, R. S., Beever, J. E. & Schook, L. B. Diversification of porcine MHC class II genes: evidence for selective advantage. Immunogenetics 61, 119–129 (2009).


    Google Scholar
     

  • Le, M. T. et al. Comprehensive and high-resolution typing of swine leukocyte antigen DQA from genomic DNA and determination of 25 new SLA class II haplotypes. Tissue Antigens 80, 528–535 (2012).


    Google Scholar
     

  • Maccari, G. et al. IPD-MHC 2.0: an improved inter-species database for the study of the major histocompatibility complex. Nucleic Acids Res. 45, D860–D864 (2017).


    Google Scholar