Title of article :
Development of polyclonal heavy chain antibodies targeting programmed death ligand-1
Author/Authors :
Oghalaie ، Akbar Venom and Biotherapeutics Molecules Laboratory - Biotechnology Research Center - Pasteur Institute of Iran , Shoari ، Alireza Venom and Biotherapeutics Molecules Laboratory - Biotechnology Research Center - Pasteur Institute of Iran , Kazemi-Lomedasht ، Fatemeh Venom and Biotherapeutics Molecules Laboratory - Biotechnology Research Center - Pasteur Institute of Iran , Rahimi-Jamnani ، Fatemeh Department of Mycobacteriology and Pulmonary Research - Pasteur Institute of Iran , Mahboudi ، Fereidoun Biotechnology Research Center - Pasteur Institute of Iran , Ghaderi ، Hajarossadat Venom and Biotherapeutics Molecules Laboratory - Biotechnology Research Center - Pasteur Institute of Iran , Hosseininejad-Chafi ، Mohammad Venom and Biotherapeutics Molecules Laboratory - Biotechnology Research Center - Pasteur Institute of Iran , Moaazami ، Reza Human Genetics Research Center - Baqiyatallah University of Medical Sciences , Ashja Ardalan ، Arghavan Venom and Biotherapeutics Molecules Laboratory - Biotechnology Research Center - Pasteur Institute of Iran , Piri-Gavgani ، Somayeh Department of Mycobacteriology and Pulmonary Research - Pasteur Institute of Iran , Shabazzadeh ، Delavar Venom and Biotherapeutics Molecules Laboratory - Biotechnology Research Center - Pasteur Institute of Iran , Behdani ، Mahdi Venom and Biotherapeutics Molecules Laboratory - Venom and Biotherapeutics Molecules Laboratory, Biotechnology Research Center, Zoonoses Research Center - Pasteur Institute of Iran
From page :
323
To page :
328
Abstract :
Programmed death ligand-1 (PD-L1, CD274 and B7-H1) has been described as a ligand for immune inhibitory receptor programmed death protein 1 (PD-1). With binding to PD-1 on activated T cells, PD-L1 can prevent T cell responses via motivating apoptosis. Consequently, it causes cancers immune evasion and helps the tumor growth; hence, PD-L1 is regarded as a therapeutic target for malignant cancers. The anti-PD-L1 monoclonal antibody targeting PD- 1/PD-L1 immune checkpoint has attained remarkable outcomes in clinical application and has turned to one of the most prevalent anti-cancer drugs. The present study aimed to develop polyclonal heavy chain antibodies targeting PD-L1via Camelus dromedarius immunization. The extra-cellular domain of human PD-L1 (hPD-L1) protein was cloned, expressed, and purified. Afterwards, this recombinant protein was utilized as an antigen for camel immunization to acquire polyclonal camelid sera versus this protein. Our outcomes showed that hPD-L1 protein was effectively expressed in the prokaryotic system. The antibody-based techniques, such as enzyme-linked immunosorbent assay, western blotting, and flow cytometry displayed that the hPD-L1 protein was detected by generated polyclonal antibody. Due to the advantages of multiepitope- binding ability, our study exhibited that camelid antibody is effective to be applied significantly for detection of PD-L1 protein in essential antibody-based studies.
Keywords :
Camelid heavy , chain antibody , Immunization , Polyclonal antibody , Programmed death ligand , 1
Journal title :
Veterinary Research Forum
Journal title :
Veterinary Research Forum
Record number :
2746665
Link To Document :
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