TY - JOUR
T1 - Establishment of C20Mab-11, a novel anti-CD20 monoclonal antibody, for the detection of B cells
AU - Furusawa, Yoshikazu
AU - Kaneko, Mika Kato
AU - Kato, Yukinari
N1 - Funding Information:
The present study was supported in part by Japan Agency for Medical Research and Development (AMED) [grant nos. JP19am0401013 (YK), JP19am0101078 (YK) and JP19ae0101028 (YK)] and by Japan Society for the Promotion of Science Grants‑in‑Aid for Scientific Research (KAKENHI) [grant. nos. 17K07299 (MKK) and 19K07705 (YK)].
Funding Information:
Cell lines. P3X63Ag8U.1 (P3U1), Chinese hamster ovary (CHO)-K1, Lec1, Lec2, Lec8, and LN229 cells were obtained from the American Type Culture Collection. Raji and BALL-1 were obtained from the Cell Resource Center for Biomedical Research (Institute of Development, Aging and Cancer, Tohoku University, Miyagi, Japan). DNA encoding the CD20 gene (IRAL012D02) was provided by the RIKEN BRC through the National BioResource Project of MEXT, Japan. The open reading frame of CD20 plus an N-terminal PA tag was subcloned into a pCAG‑Neo or pCAG‑Ble vector (FUJIFILM Wako Pure Chemical Corporation). CHO/CD20 and CHO/mock were produced by transfecting pCAG-Neo/CD20 and pCAG-Neo into CHO-K1 cells, respectively, using a Gene Pulser Xcell electroporation system (Bio-Rad Laboratories, Inc.). LN229/CD20 and LN229/mock were produced by transfecting pCAG-Ble/CD20 and pCAG-Ble into LN229 cells, respectively, using a Neon transfection system (Thermo Fisher Scientific, Inc.). Lec1/CD20 (N‑glycan‑deficient), Lec2/CD20 (sialic acid‑deficient), and Lec8/CD20 (galactose‑deficient) were produced by transfecting pCAG-Ble/CD20 into Lec1, Lec2, and Lec8 cells, respectively, using a Neon transfection system. Lec1/mock, Lec2/mock, and Lec8/mock were produced by transfecting pCAG-Ble into Lec1, Lec2, and Lec8 cells, respectively, using a Neon transfection system. The cell line BALL-1/CD20-KO (BINDS-24) was generated by transfecting CRISPR/Cas9 plasmids for CD20 (Thermo Fisher Scientific, Inc.) using a Neon transfection system. Stable transfectants were established using SH800 (Sony Corp.).
Funding Information:
The authors would like to thank Mr. Takuro Nakamura, Ms. Miyuki Yanaka and Ms. Saori Handa (Tohoku University) for technical assistance of in vitro experiments. The present study was supported in part by Japan Agency for Medical Research and Development (AMED) [grant nos. JP19am0401013 (YK), JP19am0101078 (YK) and JP19ae0101028 (YK)] and by Japan Society for the Promotion of Science Grants-in-Aid for Scientific Research (KAKENHI) [grant. nos. 17K07299 (MKK) and 19K07705 (YK)].
Publisher Copyright:
© This work is licensed under a Creative Commons Attribution 4.0 International (CC BY 4.0) License.
PY - 2020/8
Y1 - 2020/8
N2 - CD20 is one of several B-lymphocyte antigens that has been shown to be an effective target for the detection and treatment of B-cell lymphomas. Sensitive and specific monoclonal antibodies (mAbs) are required for every application used for the diagnosis of B-cell lymphoma. Although many anti-CD20 mAbs have been established, the types of applications, those anti-CD20 can be used in, are limited. In this study, we aimed to establish novel anti-CD20 mAbs to be used for broad applications, such as flow cytometry, western blot, and immunohistochemical analyses, using the Cell-Based Immunization and Screening (CBIS) method. One of the established mAbs, C20Mab-11 (IgM, kappa), detected overexpression of CD20 in CHO-K1 or LN229 cell lines, indicating that C20Mab-11 is specific for CD20. In western blot analyses, C20Mab-11 detected not only overexpression of CD20 in CHO-K1 or LN229 cell lines, but also CD20 of BALL-1 and Raji cells with both sensitivity and specificity. Furthermore, C20Mab-11 strongly stained B cells of the lymph follicle and B cell lymphomas in immunohistochemical analyses. These results indicate that C20Mab-11 develped by CBIS method, is useful for the detection of CD20 in lymphoma tissues by flow cytometry, western blot, and immunohistochemical analyses and potentially could be beneficial for the treatment of B cell lymphomas.
AB - CD20 is one of several B-lymphocyte antigens that has been shown to be an effective target for the detection and treatment of B-cell lymphomas. Sensitive and specific monoclonal antibodies (mAbs) are required for every application used for the diagnosis of B-cell lymphoma. Although many anti-CD20 mAbs have been established, the types of applications, those anti-CD20 can be used in, are limited. In this study, we aimed to establish novel anti-CD20 mAbs to be used for broad applications, such as flow cytometry, western blot, and immunohistochemical analyses, using the Cell-Based Immunization and Screening (CBIS) method. One of the established mAbs, C20Mab-11 (IgM, kappa), detected overexpression of CD20 in CHO-K1 or LN229 cell lines, indicating that C20Mab-11 is specific for CD20. In western blot analyses, C20Mab-11 detected not only overexpression of CD20 in CHO-K1 or LN229 cell lines, but also CD20 of BALL-1 and Raji cells with both sensitivity and specificity. Furthermore, C20Mab-11 strongly stained B cells of the lymph follicle and B cell lymphomas in immunohistochemical analyses. These results indicate that C20Mab-11 develped by CBIS method, is useful for the detection of CD20 in lymphoma tissues by flow cytometry, western blot, and immunohistochemical analyses and potentially could be beneficial for the treatment of B cell lymphomas.
KW - CD20
KW - Flow cytometry
KW - Immunohistochemistry
KW - Monoclonal antibody
KW - Western blotting
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U2 - 10.3892/ol.2020.11753
DO - 10.3892/ol.2020.11753
M3 - Article
AN - SCOPUS:85086855739
SN - 1792-1074
VL - 20
SP - 1961
EP - 1967
JO - Oncology Letters
JF - Oncology Letters
IS - 2
ER -