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Antidisialoganglioside ricin A-chain immunotoxins show potent antitumor effects in vitro and in a disseminated human neuroblastoma severe combined immunodeficiency mouse model.

Abstract
Several monoclonal antibodies (mAbs) were screened on different neuroblastoma cell lines to evaluate ricin A-chain immunotoxins for possible use against human neuroblastoma. Four mAbs were identified that exhibited high antitumor activity against neuroblastoma cell lines as measured in an indirect cytotoxicity assay. These mAbs, including 14G2a (antidisialoganglioside), ch14.18 (a humanized switch variant), BW704 (antidisialoganglioside), and chCE7 (anti-glycoprotein of M(r) 190,000), were subsequently linked via the bivalent linker N-succinimidyloxycarbonyl-alpha-methyl-alpha-(2-piridyldithio++ +)toluene to deglycosylated ricin A chain. The most potent immunotoxin, 14G2a.dgA, inhibited the protein synthesis of neuroblastoma cell lines IMR5 and NMB by 50% at concentrations of 6 x 10(-12) M. To test the antitumor efficacy of these immunotoxins in vivo, we developed a disseminated human neuroblastoma model in severe combined immunodeficiency mice. Treatment of tumor-bearing mice with 14G2a.dgA 12 days after tumor challenge resulted in a significant prolongation of survival as compared with phosphate-buffered saline-treated controls (16.8 versus 6.5 weeks). We conclude that ricin A-chain immunotoxins might be of potential use in the treatment of human neuroblastoma.
AuthorsC Gottstein, G Schön, S Tawadros, D Kube, U C Wargalla-Plate, M L Hansmann, H H Wacker, F Berthold, V Diehl, A Engert
JournalCancer research (Cancer Res) Vol. 54 Issue 23 Pg. 6186-93 (Dec 01 1994) ISSN: 0008-5472 [Print] United States
PMID7954465 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antibodies, Monoclonal
  • Gangliosides
  • Immunotoxins
  • sialogangliosides
  • Ricin
Topics
  • Animals
  • Antibodies, Monoclonal (immunology, therapeutic use)
  • Gangliosides (immunology)
  • Humans
  • Immunotoxins (pharmacology, therapeutic use)
  • Mice
  • Mice, SCID
  • Neoplasm Transplantation
  • Neuroblastoma (therapy)
  • Ricin (pharmacology, therapeutic use)
  • Transplantation, Heterologous

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