Strong antibody reaction against glycosphingolipids injected in liposome-embedded forms in beta3GN-T5 knockout mice.

Xiaoyan Fan, Yuji Kondo, Noriyo Tokuda, Yuhsuke Ohmi, Reiko Ando, Tomokazu Umezu, Qing Zhang, Keiko Furukawa, Kiyosumi Shibata, Akira Togayachi, Hisashi Narimatsu, Tetsuya Okajima, Koji Kikkawa, Koichi Furukawa

研究成果: Article査読

3 被引用数 (Scopus)

抄録

It is known that mutant mice of the beta-1,3-N-acetylglucosaminyltransferase gene (beta3Gn-T5) respond well to T-cell dependent and independent antigens. Here, we examined the effectiveness of anti-ganglioside antibody generation by immunization of beta3Gn-T5 mutant mice with liposome-embedded glycosphingolipids such as GD1a and GT1b. Consequently, the mutant mice showed a more efficient generation of anti-GD1a or anti-GT1b antibodies than wild-type mice in an enzyme-linked immunosorbent assay using sera during immunization. Thus, the beta3Gn-T5 deficient mutant mice proved more responsive than wild-type mice to not only protein antigens, but also to carbohydrates in glycolipids. Furthermore, about 50% of monoclonal antibodies generated using splenocytes of the immunized mutant mice were of the IgG class. Besides general high responsiveness to proteins and glycolipids, it could be expected that the mutant mice of beta3Gn-T5 would be useful in the generation of monoclonal antibodies towards lacto-/neolacto-series glycolipids, since these mutants lack lacto-/neolacto-series glycolipids. In fact, they showed a good serum response in immuno-fluorescence assay with cultured living cells when immunized by glycolipids extracted from ovarian cancer cell lines. These results suggested that beta3Gn-T5 mutant mice are useful for the generation of anti-glycolipid antigens with lacto-/neolacto-core structures expressed in cancer cells.

本文言語English
ページ(範囲)137-146
ページ数10
ジャーナルNagoya journal of medical science
73
3-4
出版ステータスPublished - 08-2011

All Science Journal Classification (ASJC) codes

  • Medicine(all)

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