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Development of Anti-Human CC Chemokine Receptor 9 Monoclonal Antibodies for Flow Cytometry.

Authors :
Nanamiya, Ren
Takei, Junko
Asano, Teizo
Tanaka, Tomohiro
Sano, Masato
Nakamura, Takuro
Yanaka, Miyuki
Hosono, Hideki
Kaneko, Mika K.
Kato, Yukinari
Source :
Monoclonal Antibodies in Immunodiagnosis & Immunotherapy. Jun2021, Vol. 40 Issue 3, p101-106. 6p.
Publication Year :
2021

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. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
21679436
Volume :
40
Issue :
3
Database :
Academic Search Index
Journal :
Monoclonal Antibodies in Immunodiagnosis & Immunotherapy
Publication Type :
Academic Journal
Accession number :
151059968
Full Text :
https://doi.org/10.1089/mab.2021.0007