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  3. Quantitative analysis of infiltrating immune cells and bovine papillomavirus type 1 E2-positive cells in equine sarcoids
 

Quantitative analysis of infiltrating immune cells and bovine papillomavirus type 1 E2-positive cells in equine sarcoids

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BORIS DOI
10.7892/boris.93920
Publisher DOI
10.1016/j.tvjl.2016.06.016
PubMed ID
27687925
Description
Sarcoids are the most frequently observed skin tumours in equids and consist of cutaneous accumulations of transformed fibroblasts. Their aetiopathogenesis is closely linked to a presumably abortive infection by bovine papillomavirus (BPV) types 1 and 2. In cattle, dermal fibropapillomas induced by BPV1/2 usually regress spontaneously due to a local, cell-mediated, immune response; however, equids appear to lack an effective immune response to BPV1/2 and mechanisms of immune evasion have been postulated. As a consequence, equine sarcoids tend to persist and are prone to recur. In this study, cryosections were analysed by immunofluorescent staining and a high content analysis system to determine the presence and distribution of CD4(+), CD8(+), FoxP3(+), RORγt(-), CD206(+) and CD14(+) cells, along with expression of the BPV1 early regulatory protein E2. A higher density of cells was positive for BPV1 E2(+) within the transformed tissue than in perilesional tissue or normal skin of horses with sarcoids and control horses. The proportion of CD8(+) cytotoxic T cells was significantly increased in perilesional and lesional tissues, whereas CD4(+) T helper cells were present in higher density only in lesional tissue compared to normal skin from horses with and without sarcoids. The proportion of pro-inflammatory CD4(+)FoxP3(+)RORγt(+) regulatory T cells was decreased in sarcoid tissue compared to perilesional, distant and control tissue. There were no significant differences in densities of CD4(+)FoxP3(+) RORγt(-) regulatory T cells between sarcoids and control tissues. Equine sarcoids are characterised by infiltrations of CD8(+) and CD4(+) T cells, with decreased representation by pro-inflammatory CD4(+)FoxP3(+)RORγt(+) regulatory T cells.
Date of Publication
2016
Publication Type
Article
Subject(s)
600 Technology > 630 Agriculture
500 Science > 570 Life sciences; biology
Language(s)
en
Contributor(s)
Geisshüsler, Helena
Departement klinische Veterinärmedizin, Pferdeklinik (ISME)
Marti, Eliane Isabelleorcid-logo
Department of Clinical Research and Veterinary Public Health, Experimentelle Klinische Forschung
Stoffel, Michael Hubertorcid-logo
Department of Clinical Research and Veterinary Public Health, Veterinär-Anatomie
Kühni, Kathrin
Department of Clinical Research and Veterinary Public Health, Veterinär-Anatomie
Stojiljkovic, Ana
Department of Clinical Research and Veterinary Public Health, Veterinär-Anatomie
von Tscharner, Claudia
Institut für Tierpathologie (ITPA)
Vidondo Curras, Beatriz Teresaorcid-logo
VPH-Institut der Universität Bern
Gerber, Vinzenz
Departement klinische Veterinärmedizin, Pferdeklinik (ISME)
Koch, Christoph
Departement klinische Veterinärmedizin, Pferdeklinik (ISME)
Additional Credits
Department of Clinical Research and Veterinary Public Health, Veterinär-Anatomie
Institut für Tierpathologie (ITPA)
VPH-Institut der Universität Bern
Departement klinische Veterinärmedizin, Pferdeklinik (ISME)
Department of Clinical Research and Veterinary Public Health, Experimentelle Klinische Forschung
Series
Veterinary journal
Publisher
Elsevier
ISSN
1090-0233
Access(Rights)
restricted
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