Programmed-cell death ligand 1 (PD-L1) expression in equine sarcoids and squamous cell carcinoma

被引:0
|
作者
Pimenta, Jose [1 ,2 ,3 ,6 ]
Prada, Justina [1 ,2 ,4 ]
Pires, Isabel [1 ,2 ,4 ]
Cotovio, Mario [1 ,2 ,5 ]
机构
[1] Univ Tras os Montes & Alto Douro, CECAV Vet & Anim Res Ctr, Vila Real, Portugal
[2] Associate Lab Anim & Vet Sci AL4AnimalS, Vila Real, Portugal
[3] EUVG Vasco da Gama Univ Sch, CIVG Vasco da Gama Res Ctr, Coimbra, Portugal
[4] Univ Tras os Montes & Alto Douro, Vet Sci Dept, Vila Real, Portugal
[5] Lusofona Univ, Fac Vet Med, Lisbon, Portugal
[6] EUVG Vasco da Gama Univ Sch, Coimbra, Portugal
关键词
Equine; Immunotherapy; PD-L1; Sarcoid; SCC;
D O I
10.5455/OVJ.2024.v14.i6.16
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Background: Sarcoids and squamous cell carcinomas (SCCs) are the most concerning equine oncological diseases. Both tumors are challenging to manage due to their invasive behavior and high prevalence of recurrences. Furthermore, SCCs have a propensity to metastasize. Programed cell-death ligand 1 (PD-L1) has been one of the main therapeutic targets for immunotherapy in various human tumors. PD-L1 research in equine tumors is scarce and more efforts are necessary to understand the potential of this biomarker as a therapeutical target. Aim: Evaluate the immunohistochemical expression of PD-L1 in equine sarcoids and SCC. Methods: Thirteen equine tumors (seven sarcoids and 6 SCCs) were tested by immunohistochemistry and evaluated semi quantitatively to assess the percentage of positive cells. Results: None of the sarcoids presented PD-L1 expression. Regarding SCC, 2 tumors presented <10% of labeled cells; 2 tumors presented 10%-25% of labeled cells and 2 tumors presented 25%-50% of labeled cells. There were statistically significant differences between sarcoids and SCC regarding the expression of PD-L1. Conclusion: Our results point to the fact that PD-L1 could be a potential therapeutic target against SCC, and also encourage in-depth studies in this area, with larger sample sizes.
引用
收藏
页码:1476 / 1482
页数:7
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