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Cited by 174

The DOI matches its Crossref record; 8 of the 8 references it cites were found in a registry or an index.

Engineering Chinese hamster ovary cells to maximize effector function of produced antibodies using FUT8 siRNA

Mori, Katsuhiro, Kuni‐Kamochi, Reiko, Yamane‐Ohnuki, Naoko, Wakitani, Masako, Yamano, Kazuya, Imai, Harue, Kanda, Yutaka, Niwa, Rinpei, Iida, Shigeru, Uchida, Kazuhisa, Shitara, Kenya, Satoh, Mitsuo·2004·Biotechnology and Bioengineering

Abstract

We explored the possibility of converting established antibody‐producing cells to cells producing high antibody‐dependent cellular cytotoxicity (ADCC) antibodies. The conversion was made by constitutive expression of small interfering RNA (siRNA) against α1,6 fucosyltransferase (FUT8). We found two effective siRNAs, which reduce FUT8 mRNA expression to 20% when introduced into Chinese hamster ovary (CHO)/DG44 cells. Selection for Lens culinaris agglutinin (LCA)‐resistant clones after introduction of the FUT8 siRNA expression plasmids yields clones producing highly defucosylated (≈60%) antibody with over 100‐fold higher ADCC compared to antibody produced by the parental cells (≈10% defucosylated). Moreover, the selected clones remain stable, producing defucosylated antibody even in serum‐free fed‐batch culture. Our results demonstrate that constitutive FUT8 siRNA expression can control the oligosaccharide structure of recombinant antibody produced by CHO cells to yield antibodies with dramatically enhanced ADCC. © 2004 Wiley Periodicals, Inc.

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Metadata

Authors
Mori, K., Kuni‐Kamochi, R., Yamane‐Ohnuki, N., Wakitani, M., Yamano, K., Imai, H., Kanda, Y., Niwa, R., Iida, S., Uchida, K., Shitara, K., & Satoh, M.
Venue
Biotechnology and Bioengineering
Publisher
Wiley
Published
2004-10-28
Volume
88
Issue
7
Pages
901-908
ISSN
  • 0006-3592 (ISSN-L)
  • 1097-0290
OpenAlex
W2129658913
Cited by
174
References
8
FWCI
3.39
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Engineering Chinese hamster ovary cells to maximize effector function of produced antibodies using FUT8 siRNA. https://app.cochat.ai/papers/10.1002/bit.20326
The paper
Mori, K., Kuni‐Kamochi, R., Yamane‐Ohnuki, N., Wakitani, M., Yamano, K., Imai, H., Kanda, Y., Niwa, R., Iida, S., Uchida, K., Shitara, K., & Satoh, M. (2004). Engineering Chinese hamster ovary cells to maximize effector function of produced antibodies using FUT8 siRNA. Biotechnology and Bioengineering. https://doi.org/10.1002/bit.20326

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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