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Immunogenicity analysis of BPV-1 positive equine sarcoid-derived cultured fibroblasts.

Authors :
Gysens, Lien
Depuydt, Eva
Patruno, Marco
Haspeslagh, Maarten
Spaas, Jan H.
Martens, Ann
Source :
Veterinary Immunology & Immunopathology. Feb2023, Vol. 256, pN.PAG-N.PAG. 1p.
Publication Year :
2023

Abstract

Sarcoids are the most common equine skin tumours Although they do not metastasize, they can be locally aggressive and cause significant clinical symptoms in affected horses. Despite being common, very little is known about the host immune response and the biological mechanisms underlying persistence and recurrence of equine sarcoids. The latter reflects the need for further research in this field. This in-vitro study used sarcoid explants from horses with naturally occurring sarcoids (n = 12) to evaluate the induction of a humoral immune response directed against equine sarcoid-derived bovine papilloma-virus (BPV)− 1 infected fibroblasts using a flow cytometric crossmatch assay. The presence of antibodies against exogenous bovine serum albumin (BSA) and fibroblast-like mesenchymal stromal cells (MSCs) was also evaluated by ELISA and flow cytometry, respectively. The viral load in the sarcoid explants, the corresponding cultured sarcoid fibroblasts, and matched peripheral blood mononuclear cells (PBMCs) from affected horses were determined by quantitative BPV-1/− 2 PCR analysis. Antibodies against autologous sarcoid cells were present in six out of twelve sarcoid-affected horses. Serum from all horses showed cross reactivity with allogeneic sarcoid cells, while only a part reacted with BSA or MSCs. Screening of host PBMCs demonstrated the absence of BPV E1 nucleic acids. Statistical analysis revealed a significantly higher mean viral load in the parental sarcoid tissue compared to the low passage fibroblasts (P < 0.001). These results support the hypothesis that sarcoid-affected horses may develop antibodies recognizing tumour-specific antigens. In contrast to sarcoid explants, equine PBMCs do not seem to contain complete BPV genomes. These results provide a basis for future investigations on the clinical relevance of these antibodies. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
01652427
Volume :
256
Database :
Academic Search Index
Journal :
Veterinary Immunology & Immunopathology
Publication Type :
Academic Journal
Accession number :
161441334
Full Text :
https://doi.org/10.1016/j.vetimm.2023.110547