# Age-dependent differences in type I interferon, IL-12 and pro-inflammatory cytokine production by porcine peripheral blood mononuclear cells in response to pseudorabies virus-infected cells

**Authors:** Manon S. C. Claeys, Simon G. A. L. Brabant, Stijn Rosschaert, Cliff Van Waesberghe, Herman W. Favoreel

PMC · DOI: 10.3389/fimmu.2025.1596490 · Frontiers in Immunology · 2025-07-03

## TL;DR

Young pigs have weaker immune responses to a virus compared to older pigs, which may explain why the disease is more severe in newborns.

## Contribution

The study identifies age-related differences in cytokine production in pigs infected with pseudorabies virus, offering insights for improving neonatal immune responses.

## Key findings

- PBMCs from young pigs show low IFN-α and IL-12 production in response to PRV.
- Newborn piglets exhibit high IL-6 and IL-10 levels, suggesting suppressed Th1 immune responses.
- Age-related cytokine shifts correlate with changes in PRV symptom severity in pigs.

## Abstract

Pseudorabies virus is a porcine alphaherpesvirus that causes devastating disease with high mortality in young piglets but much milder, mainly respiratory, problems in older pigs. Here, we report marked age-dependent differences in the cytokine response profile of primary porcine peripheral blood mononuclear cells (PBMCs) to pseudorabies virus (PRV)-infected cells. Notably, IFN-α and IL-12 production in response to PRV remains low to almost undetectable in piglets up to 8.5 weeks of age, followed by a marked increase in older piglets, which coincides with age-related shifts in PRV symptomatology. Additionally, we found that PBMC from newborn piglets exhibit a high IL-6 and IL-10 production which, in combination with the low IL-12 levels, suggests a suppressed Th1 immune response, similar to neonatal humans and mice. Our results reveal a remarkable age-dependent difference in PBMC cytokine response to PRV and provide a basis to identify cytokines or adjuvants that shift the neonatal immune response towards a Th1 response, potentially improving outcomes of severe viral infections in the neonatal period in both pigs and humans.

## Linked entities

- **Proteins:** IFN1@ (interferon, type 1, cluster), IL12 (Interleukin 12 level), IL6 (interleukin 6), IL10 (interleukin 10)
- **Diseases:** pseudorabies (MONDO:0005932)
- **Species:** Sus scrofa (taxon 9823)

## Full-text entities

- **Genes:** IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, IL12B (interleukin 12B) [NCBI Gene 3593] {aka CLMF, CLMF2, IL-12B, IMD28, IMD29, NKSF}, IFNA1 (interferon alpha 1) [NCBI Gene 3439] {aka IFL, IFN, IFN-ALPHA, IFN-alphaD, IFNA13, IFNA@}
- **Diseases:** viral infections (MESH:D014777), inflammatory (MESH:D007249)
- **Species:** Sus scrofa (pig, species) [taxon 9823], Homo sapiens (human, species) [taxon 9606], Suid alphaherpesvirus 1 (no rank) [taxon 10345], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12267268/full.md

## References

87 references — full list in the complete paper: https://tomesphere.com/paper/PMC12267268/full.md

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Source: https://tomesphere.com/paper/PMC12267268