ASFV Proteins Presented at the Surface of T7 Phages Induce Strong Antibody Responses and Immune Cell Proliferation in Sus scrofa

<b>Background/Objectives:</b> African swine fever (ASF) causes massive global swine industry losses with no effective vaccine available. This study constructed T7 phages displaying key ASFV proteins to evaluate their potential as an ASF vaccine by assessing viral shedding and immune responses in pigs. <b>Methods:</b> Five ASFV proteins were displayed on T7 phages to form VLPs (ASFV-SC-T7 group), with soluble proteins (ASFV-SC group) and PBS as controls; 9 piglets were immunized, boosted at 28 days, challenged with virulent ASFV, and assessed via ELISA, flow cytometry, and real-time PCR. <b>Results:</b> ASFV-SC-T7 induced more high-titer antibodies and elevated monocytes/CD8<sup>+</sup> T cells, but all groups developed ASF lesions, with ASFV-SC-T7 having higher lung/mesenteric lymph node viral loads and no survival improvement (only delayed fever). <b>Conclusions:</b> T7 phage-displayed ASFV proteins activate strong immunity, confirming T7 phages as a viable delivery platform, but failed to protect against virulent ASFV, requiring future optimization of antigens and regimens.

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Publication Details

Journal
Vaccines
Published
2025-12-19
DOI
https://doi.org/10.3390/vaccines14010004
Primary Topic
Animal Disease Management and Epidemiology
Type
article
Field-Weighted Citation Impact
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article

ASFV Proteins Presented at the Surface of T7 Phages Induce Strong Antibody Responses and Immune Cell Proliferation in Sus scrofa

Vaccines
Animal Disease Management and Epidemiology
article

ASFV Proteins Presented at the Surface of T7 Phages Induce Strong Antibody Responses and Immune Cell Proliferation in Sus scrofa

article en

Abstract

<b>Background/Objectives:</b> African swine fever (ASF) causes massive global swine industry losses with no effective vaccine available. This study constructed T7 phages displaying key ASFV proteins to evaluate their potential as an ASF vaccine by assessing viral shedding and immune responses in pigs. <b>Methods:</b> Five ASFV proteins were displayed on T7 phages to form VLPs (ASFV-SC-T7 group), with soluble proteins (ASFV-SC group) and PBS as controls; 9 piglets were immunized, boosted at 28 days, challenged with virulent ASFV, and assessed via ELISA, flow cytometry, and real-time PCR. <b>Results:</b> ASFV-SC-T7 induced more high-titer antibodies and elevated monocytes/CD8<sup>+</sup> T cells, but all groups developed ASF lesions, with ASFV-SC-T7 having higher lung/mesenteric lymph node viral loads and no survival improvement (only delayed fever). <b>Conclusions:</b> T7 phage-displayed ASFV proteins activate strong immunity, confirming T7 phages as a viable delivery platform, but failed to protect against virulent ASFV, requiring future optimization of antigens and regimens.

VaccinesVol. 14(1)
Tianjin University (CN), China Institute of Veterinary Drug Control (CN)
Openalex Percentile: Top 31%
Animal Disease Management and Epidemiology
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