Cross-reactivity of anti-human programmed cell death ligand 1 (PD-L1) monoclonal antibody, clone 28-8 against feline PD-L1

被引:2
作者
Nishibori, Shoma [1 ]
Sakurai, Masashi [2 ]
Kagawa, Yumiko [3 ]
Uchida, Kazuyuki [4 ]
Nakagawa, Takayuki [5 ]
Igase, Masaya [1 ]
Mizuno, Takuya [1 ,6 ]
机构
[1] Yamaguchi Univ, Joint Fac Vet Med, Lab Mol Diagnost & Therapeut, Yamaguchi, Japan
[2] Yamaguchi Univ, Joint Fac Vet Med, Lab Vet Pathol, Yamaguchi, Japan
[3] North Lab, Sapporo, Hokkaido, Japan
[4] Univ Tokyo, Grad Sch Agr & Life Sci, Lab Vet Pathol, Tokyo, Japan
[5] Univ Tokyo, Grad Sch Agr & Life Sci, Lab Vet Surg, Tokyo, Japan
[6] Yamaguchi Univ, Joint Fac Vet Med, Lab Mol Diagnost & Therapeut, 1677-1 Yoshida, Yamaguchi, Yamaguchi 7538511, Japan
关键词
antibody; feline; immune checkpoint; immunohistochemistry; programmed cell death ligand 1; IMMUNOHISTOCHEMISTRY ASSAYS; IMMUNODEFICIENCY VIRUS; LUNG-CANCER; B7; FAMILY; EXPRESSION; RECEPTOR; SYSTEM; MEMBER; B7-H1;
D O I
10.1292/jvms.23-0003
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
. Immunotherapy is a breakthrough in human cancer therapy and has become a major concern in veterinary oncology. However, in cats, many unclear points of the tumor microenvironment exist, including immune checkpoint molecules. A reason is that very few monoclonal antibodies have been proven to react with feline molecules. Therefore, this study investigated whether antihuman programmed cell death ligand 1 (PD-L1) monoclonal antibody, clone 28-8, which is currently commercially available, can also recognize feline PD-L1 by flow cytometry, immunoprecipitation, and immunohistochemical (IHC) staining. We confirmed that the antibody's specificity by flow cytometry and immunoprecipitation using NIH3T3 cells transfected with feline PD-L1. Additionally, we revealed that PD-L1 was expressed on the surface of some feline cell lines by flow cytometry and clone 28-8 antibody unbound to the cells where feline PD-L1 was knocked out. Furthermore, IHC analysis revealed that PD-L1 was expressed in macrophages in the spleen and lymph nodes from healthy cats and mast cell tumor cells. Therefore, we indicated that the clone 28-8 antibody is a valuable tool in detecting feline PD-L1, and further analysis of tumor tissues is expected in the future.
引用
收藏
页码:592 / 600
页数:9
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