Detecting exosomal PD-L1 secreted by cancer cells

Detecting exosomal PD-L1 secreted by cancer cells



Exosomes is the extracellular vesicles secreted by all cells. Evidences accumulated that exosomes implicate in various diseases including cancer metastasis and neurodegeneration diseases. PD-L1 is an immune checkpoint inhibitor that keep T cells from attacking other cells in the body. Many cancer cells overexpress PD-L1 to escape the immunological attack.

The exosomal PD-L1 has been isolated in multiple cancer cells. Recently, Chen et al. elucidated the regulation and immunosuppressive function of exosomal PD-L1 and published their result in Nature. They found that IFNγ treatment enhances the levels of PD-L1 in exosomes. In mouse model, exosomal PD-L1 inhibits CD8+ T cells and facilitates the cancer progression. Moreover, the authors examined the exosomel PD-L1 levels in melanoma patients during anti-PD-1 therapy and found that the pretreatment level of exosomal PD-L1 was higher in non-responders which was associated with poor prognosis. Their study provides a rationale for the application of exosomal PD-L1 as a predictor for anti-PD-1 therapy.

arigo offers excellent ELISA kits to detect exosomal PD-L1 level. In addition, more quality antibodies and ELISA kits are available for facilitating related studies.


● Detecting exosomal PD-L1

Human PD-L1 ELISA Kit (ARG81929)
Sensitivity: 31.25 pg/ml 
Samples: Serum, Plasma, Cell culture sup.

Mouse PD-L1 ELISA Kit (ARG81930)
Sensitivity: 15.6 pg/ml 
Samples: Serum, Plasma, Cell culture sup.

 

 

● Exosome Antibody Panel (ARG30348)

- Includes exosome marker CD63 antibody for detecting tetraspanin
- Includes exosome marker TSG101 antibody for detecting ESCRT complex
- Includes exosome exclusion marker GM130 antibody
- Works on human samples

Component Reactivity Application Pkg
CD63 antibody Hu ICC/IF, IHC-P, WB 20 ul
TSG101 antibody Hu, Ms, Rat FACS, ICC/IF, IHC-P, WB 20 ul
GM130 antibody Hu, Ms, Rat, Cow, Dog, Mk ICC/IF, IHC-P, IP, WB 20 ul

 


Reference: Chen et al., (2018) Nature. 560(7718):382-386.