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Sensing antibody functions with a novel CCR8-responsive engineered cell.
Hao, Jianyu; Lv, Yitong; Xiao, Xufeng; Li, Lidan; Yu, Changyuan.
Affiliation
  • Hao J; College of Life Science and Technology, Beijing University of Chemical Technology, Beijing, China.
  • Lv Y; College of Life Science and Technology, Beijing University of Chemical Technology, Beijing, China.
  • Xiao X; Jiangsu Key Laboratory of Phylogenomics and Comparative Genomics, Jiangsu Normal University, Xuzhou, China.
  • Li L; National Clinical Research Center for Infectious Diseases, Shenzhen Third People's Hospital, The Second Affiliated Hospital of Southern University of Science and Technology, Shenzhen, China.
  • Yu C; College of Life Science and Technology, Beijing University of Chemical Technology, Beijing, China.
Acta Biochim Pol ; 71: 12185, 2024.
Article in En | MEDLINE | ID: mdl-38721308
ABSTRACT
Human chemokine receptor 8 (CCR8) is a promising drug target for immunotherapy of cancer and autoimmune diseases. Monoclonal antibody-based CCR8 targeted treatment shows significant inhibition in tumor growth. The inhibition of CCR8 results in the improvement of antitumor immunity and patient survival rates by regulating tumor-resident regulatory T cells. Recently monoclonal antibody drug development targeting CCR8 has become a research hotspot, which also promotes the advancement of antibody evaluation methods. Therefore, we constructed a novel engineered customized cell line HEK293-cAMP-biosensor-CCR8 combined with CCR8 and a cAMP-biosensor reporter. It can be used for the detection of anti-CCR8 antibody functions like specificity and biological activity, in addition to the detection of antibody-dependent cell-mediated cytotoxicity and antibody-dependent-cellular-phagocytosis. We obtained a new CCR8 mAb 22H9 and successfully verified its biological activities with HEK293-cAMP-biosensor-CCR8. Our reporter cell line has high sensitivity and specificity, and also offers a rapid kinetic detection platform for evaluating anti-CCR8 antibody functions.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biosensing Techniques / Cyclic AMP / Receptors, CCR8 / Antibodies, Monoclonal Limits: Humans Language: En Journal: Acta Biochim Pol Year: 2024 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biosensing Techniques / Cyclic AMP / Receptors, CCR8 / Antibodies, Monoclonal Limits: Humans Language: En Journal: Acta Biochim Pol Year: 2024 Document type: Article Affiliation country: