1. Neonatal porcine blood derived dendritic cell subsets show activation after TLR2 or TLR9 stimulation.
- Author
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Vreman S, Auray G, Savelkoul HFJ, Rebel A, Summerfield A, and Stockhofe-Zurwieden N
- Subjects
- Animals, Animals, Newborn, Antigen Presentation, Antigens, CD metabolism, Cell Differentiation, Cell Separation, Cells, Cultured, Flow Cytometry, Lipoproteins immunology, Oligodeoxyribonucleotides immunology, Dendritic Cells immunology, Interleukin-12 metabolism, Swine physiology, Toll-Like Receptor 2 metabolism, Toll-Like Receptor 9 metabolism
- Abstract
The present study investigated the innate immune response in vitro to determine porcine neonate responses with Toll-like receptor (TLR)2 ligand (Pam3Cys) or TLR9 ligand (CpG) and compared these with adults. We identified the same phenotypically defined dendritic cell (DC) subsets and DC proportions in porcine neonate and adult blood by flow cytometry, which were plasmacytoid DCs (pDCs): CD14
- CD4+ CD172a+ CADM1- ) and conventional DCs (cDCs), being further divided into a cDC1 (CD14- CD4- CD172alow CADM1+ ) and a cDC2 (CD14- CD4- CD172a+ CADM1+ ) subset. With neonatal cells, the TLR2 ligand induced a stronger TNF expression in monocytes and pDCs, and a stronger CD80/86 upregulation in cDC1, when compared to adult cells. Furthermore, in neonatal mononuclear cells TLR9 ligand was more potent at inducing IL12p40 mRNA expression. These results indicate clear responses of porcine neonatal antigen presenting cells after TLR2 and TLR9 stimulation, suggesting that corresponding ligands could be promising candidates for neonatal adjuvant application., (Copyright © 2018 Elsevier Ltd. All rights reserved.)- Published
- 2018
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