| Literature DB >> 34161159 |
Ren Nanamiya1, Junko Takei1, Teizo Asano1, Tomohiro Tanaka1, Masato Sano1, Takuro Nakamura1, Miyuki Yanaka1, Hideki Hosono1, Mika K Kaneko1, Yukinari Kato1,2.
Abstract
CC chemokine receptor 9 (CCR9) belongs to the beta chemokine receptor family and is mainly distributed on the surface of immature T lymphocytes and enterocytes. This receptor is highly expressed in rheumatoid arthritis, colitis, type 2 diabetes, and various tumors. Therefore, more sensitive monoclonal antibodies (mAbs) need to be developed to predict the prognosis of many high CCR9 expression diseases. Because CCR9 is a structurally unstable G protein-coupled receptor, it has been difficult to develop anti-CCR9 mAbs using the traditional method. This study developed anti-human CCR9 (hCCR9) mAbs for flow cytometry using a Cell-Based Immunization and Screening (CBIS) method. Two mice were immunized with hCCR9-overexpressed Chinese hamster ovary (CHO)-K1 cells (CHO/hCCR9), and hybridomas showing strong signals from CHO/hCCR9 and no signals from CHO-K1 cells were selected by flow cytometry. We established an anti-hCCR9 mAb, C9Mab-1 (IgG1, kappa), which detected hCCR9 in MOLT-4 leukemia T lymphoblast cells and CHO/hCCR9 cells by flow cytometry. Our study showed that an anti-hCCR9 mAb was developed more rapidly by the CBIS method than the previous method.Entities:
Keywords: CBIS; CCR9; flow cytometry; monoclonal antibody
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Year: 2021 PMID: 34161159 DOI: 10.1089/mab.2021.0007
Source DB: PubMed Journal: Monoclon Antib Immunodiagn Immunother ISSN: 2167-9436