Targeting Porcine Macrophages: The Role of Immune Modulators Against African Swine Fever Virus.
- 1Department of Veterinary Medicine, University of Sassari, 07100 Sassari, Italy.
- 2Department of Animal Health, Istituto Zooprofilattico Sperimentale della Sardegna, 07100 Sassari, Italy.
Abstract
African swine fever (ASF) is a highly lethal disease affecting domestic pigs and wild boar, with no safe vaccines available. Macrophages are the primary target cells of African swine fever virus (ASFV), and infection impairs their antiviral functions, thereby facilitating efficient viral replication within these cells and rapid dissemination in the host. This review analyzes host-directed immunomodulatory strategies to functionally reprogram macrophages and restore their defenses. We summarize several classes of immunomodulants, including bacteria, Toll-like receptor (TLR-) agonists, recombinant cytokines, and natural compounds. First, we report recent work on a heat-inactivated bacterium isolated from warthog microbiota: Rothia nasimurium, which polarizes macrophages toward an antiviral phenotype and restricts ASFV replication in vitro. However, as a live-attenuated vaccine (LAV) adjuvant in vivo, it compromises protection by limiting LAV replication. On the contrary, extracellular TLR-2 and TLR-4 ligands induce pro-inflammatory polarization without reducing replication, suggesting that they can safely enhance the poor immunogenicity of inactivated or highly attenuated vaccine candidates. Conversely, intracellular TLR-3, TLR-7/8, and TLR-9 agonists induce type I interferon pathways, and other studies have shown that type I IFNs can restrict ASFV replication. However, direct experimental studies investigating these synthetic ligands against ASFV are currently lacking. Finally, we report that natural compounds like tetrandrine, berbamine, and fangchinoline are able to inhibit ASFV replication in vitro, but they can also modulate the macrophage's immune responsiveness, preventing hyper-inflammation. Targeted immunomodulation may be fundamental to designing effective strategies against ASF. A fine-tuned orchestration of host immunity is required to control viral replication without compromising vaccine efficacy, contributing to the development of safe vaccines or alternative therapeutic tools for this fatal hemorrhagic disease.
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BibTeX
@article{candiano2026targeting,
title = {{Targeting Porcine Macrophages: The Role of Immune Modulators Against African Swine Fever Virus.}},
author = {Edoardo Candiano and Bruno Tilocca and Giulia Franzoni},
journal = {Vaccines},
year = {2026},
month = oct,
doi = {10.3390/vaccines14100904},
url = {https://europepmc.org/article/MED/42931433},
note = {CC BY},
}
RIS
TY - JOUR
TI - Targeting Porcine Macrophages: The Role of Immune Modulators Against African Swine Fever Virus.
AU - Edoardo Candiano
AU - Bruno Tilocca
AU - Giulia Franzoni
PY - 2026
DA - 2026/10/16
JO - Vaccines
DO - 10.3390/vaccines14100904
UR - https://europepmc.org/article/MED/42931433
AB - African swine fever (ASF) is a highly lethal disease affecting domestic pigs and wild boar, with no safe vaccines available. Macrophages are the primary target cells of African swine fever virus (ASFV), and infection impairs their antiviral functions, thereby facilitating efficient viral replication within these cells and rapid dissemination in the host. This review analyzes host-directed immunomodulatory strategies to functionally reprogram macrophages and restore their defenses. We summarize several classes of immunomodulants, including bacteria, Toll-like receptor (TLR-) agonists, recombinant cytokines, and natural compounds. First, we report recent work on a heat-inactivated bacterium isolated from warthog microbiota: Rothia nasimurium, which polarizes macrophages toward an antiviral phenotype and restricts ASFV replication in vitro. However, as a live-attenuated vaccine (LAV) adjuvant in vivo, it compromises protection by limiting LAV replication. On the contrary, extracellular TLR-2 and TLR-4 ligands induce pro-inflammatory polarization without reducing replication, suggesting that they can safely enhance the poor immunogenicity of inactivated or highly attenuated vaccine candidates. Conversely, intracellular TLR-3, TLR-7/8, and TLR-9 agonists induce type I interferon pathways, and other studies have shown that type I IFNs can restrict ASFV replication. However, direct experimental studies investigating these synthetic ligands against ASFV are currently lacking. Finally, we report that natural compounds like tetrandrine, berbamine, and fangchinoline are able to inhibit ASFV replication in vitro, but they can also modulate the macrophage's immune responsiveness, preventing hyper-inflammation. Targeted immunomodulation may be fundamental to designing effective strategies against ASF. A fine-tuned orchestration of host immunity is required to control viral replication without compromising vaccine efficacy, contributing to the development of safe vaccines or alternative therapeutic tools for this fatal hemorrhagic disease.
SN - 2076-393X
ER -