Skip to main content
Journal cover image

Affinity-matured anti-glycoprotein NMB recombinant immunotoxins targeting malignant gliomas and melanomas.

Publication ,  Journal Article
Kuan, C-T; Wakiya, K; Keir, ST; Li, J; Herndon, JE; Pastan, I; Bigner, DD
Published in: Int J Cancer
July 1, 2011

Glycoprotein NMB (GPNMB), a transmembrane glycoprotein highly expressed in high-grade gliomas (HGGs), is an attractive target in cancer immunotherapy. We isolated a GPNMB-specific scFv clone, G49, from a human synthetic phage-display library. To obtain mutant single-chain variable-fragment antibodies (scFvs) with improved affinity and immunotoxins with increased activity, we subjected G49 to in vitro affinity maturation by a complementarity-determining-region (CDR) random-mutagenesis technique. Using light-chain CDR3 mutagenesis, cell-based panning by phage display, subsequent heavy-chain CDR1 mutagenesis, and flow-cytometric selection by yeast-surface display, we generated the mutant scFv clone 902V, with an overall 11-fold increase in affinity for GPNMB. Clone 902V was further randomized throughout the whole scFv by error-prone PCR, and one mutant, F6V, was selected by yeast-surface display. F6V scFv, differing from 902V by one amino-acid change in the light-chain CDR2, exhibited an affinity for GPNMB of 0.30 nM. The F6V mutant scFv clone was fused with a truncated form of Pseudomonas exotoxin A to form the immunotoxin F6V-PE38. F6V-PE38 demonstrated significant protein-synthesis-inhibition activity on GPNMB-expressing glioma and malignant melanoma cells (IC(50) = 0.5 ng/ml [8 pM]), a 60-fold improvement over G49 activity, but no cytotoxicity on GPNMB-negative cells. Furthermore, F6V-PE38 exhibited significant antitumor activity against subcutaneous malignant glioma xenografts in two nude-mouse models and a melanoma neoplastic meningitis model in athymic rats. These GPNMB-specific scFv antibodies and immunotoxins hold promise as reagents in targeted therapy for HGGs and other GPNMB-expressing malignancies.

Duke Scholars

Altmetric Attention Stats
Dimensions Citation Stats

Published In

Int J Cancer

DOI

EISSN

1097-0215

Publication Date

July 1, 2011

Volume

129

Issue

1

Start / End Page

111 / 121

Location

United States

Related Subject Headings

  • Surface Plasmon Resonance
  • Recombinant Fusion Proteins
  • Oncology & Carcinogenesis
  • Mice, Nude
  • Mice
  • Membrane Glycoproteins
  • Melanoma
  • Immunotoxins
  • Humans
  • Glioma
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Kuan, C.-T., Wakiya, K., Keir, S. T., Li, J., Herndon, J. E., Pastan, I., & Bigner, D. D. (2011). Affinity-matured anti-glycoprotein NMB recombinant immunotoxins targeting malignant gliomas and melanomas. Int J Cancer, 129(1), 111–121. https://doi.org/10.1002/ijc.25645
Kuan, Chien-Tsun, Kenji Wakiya, Stephen T. Keir, Jianjun Li, James E. Herndon, Ira Pastan, and Darell D. Bigner. “Affinity-matured anti-glycoprotein NMB recombinant immunotoxins targeting malignant gliomas and melanomas.Int J Cancer 129, no. 1 (July 1, 2011): 111–21. https://doi.org/10.1002/ijc.25645.
Kuan C-T, Wakiya K, Keir ST, Li J, Herndon JE, Pastan I, et al. Affinity-matured anti-glycoprotein NMB recombinant immunotoxins targeting malignant gliomas and melanomas. Int J Cancer. 2011 Jul 1;129(1):111–21.
Kuan, Chien-Tsun, et al. “Affinity-matured anti-glycoprotein NMB recombinant immunotoxins targeting malignant gliomas and melanomas.Int J Cancer, vol. 129, no. 1, July 2011, pp. 111–21. Pubmed, doi:10.1002/ijc.25645.
Kuan C-T, Wakiya K, Keir ST, Li J, Herndon JE, Pastan I, Bigner DD. Affinity-matured anti-glycoprotein NMB recombinant immunotoxins targeting malignant gliomas and melanomas. Int J Cancer. 2011 Jul 1;129(1):111–121.
Journal cover image

Published In

Int J Cancer

DOI

EISSN

1097-0215

Publication Date

July 1, 2011

Volume

129

Issue

1

Start / End Page

111 / 121

Location

United States

Related Subject Headings

  • Surface Plasmon Resonance
  • Recombinant Fusion Proteins
  • Oncology & Carcinogenesis
  • Mice, Nude
  • Mice
  • Membrane Glycoproteins
  • Melanoma
  • Immunotoxins
  • Humans
  • Glioma