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Increased binding affinity enhances targeting of glioma xenografts by EGFRvIII-specific scFv.

Publication ,  Journal Article
Kuan, CT; Wikstrand, CJ; Archer, G; Beers, R; Pastan, I; Zalutsky, MR; Bigner, DD
Published in: Int J Cancer
December 15, 2000

Combinatorial variation of CDR3 of V(H) and V(L), followed by phage display, was used to select affinity mutants of the parental anti-epidermal growth factor receptor-vIII (EGFRvIII) scFv MR1. One mutant, MR1-1(scFv), had increased specific binding affinity for EGFRvIII. It was produced and radiolabeled, and its biodistribution was evaluated in human glioma-bearing athymic mice. MR1-1 targeted the same EGFRvIII epitope as MR1 with an approximately 15-fold higher affinity (K(d) = 1.5 x 10(-9) M) measured by surface resonance analysis. Labeling with (131)I or (125)I was performed, and the immunoreactive fraction of the labeled MR1-1(scFv) was 50% to 55%. After incubation at 37 degrees C for 4 days, the binding affinity was maintained at 60% of initial levels. The specificity of MR1-1 for EGFRvIII was demonstrated in vitro by flow cytometry and incubation of FITC-labeled scFv with the EGFRvIII-expressing U87MG. DeltaEGFR cell line or with the EGFRvIII-negative U87MG cell line in the presence or absence of competing unlabeled MR1-1(scFv). We also investigated the internalization and processing of MR1-1 compared with MR1; MR1-1 exhibited levels of both cell surface retention and internalization up to 5 times higher than those by MR1. In biodistribution studies performed in athymic mice bearing s.c. U87MG. DeltaEGFR tumor xenografts, animals received paired-label intratumoral infusions of (131)I-labeled MR1-1(scFv) and (125)I-labeled MR1(scFv). Our results showed an up to 244% +/- 77% increase in tumor uptake for MR1-1 compared with that for MR1. The improved tumor retention of MR1-1(scFv) combined with its rapid clearance from normal tissues also resulted in sustained higher tumor:normal organ ratios. These results suggest that the improved affinity of MR1-1 can significantly impact in vivo glioma-specific targeting and immunotherapy.

Duke Scholars

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Published In

Int J Cancer

DOI

ISSN

0020-7136

Publication Date

December 15, 2000

Volume

88

Issue

6

Start / End Page

962 / 969

Location

United States

Related Subject Headings

  • Transplantation, Heterologous
  • Tissue Distribution
  • Oncology & Carcinogenesis
  • Mice, Nude
  • Mice, Inbred BALB C
  • Mice
  • Iodine Radioisotopes
  • Immunotoxins
  • Immunoglobulin Variable Region
  • Glioma
 

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Kuan, C. T., Wikstrand, C. J., Archer, G., Beers, R., Pastan, I., Zalutsky, M. R., & Bigner, D. D. (2000). Increased binding affinity enhances targeting of glioma xenografts by EGFRvIII-specific scFv. Int J Cancer, 88(6), 962–969. https://doi.org/10.1002/1097-0215(20001215)88:6<962::aid-ijc20>3.0.co;2-u
Kuan, C. T., C. J. Wikstrand, G. Archer, R. Beers, I. Pastan, M. R. Zalutsky, and D. D. Bigner. “Increased binding affinity enhances targeting of glioma xenografts by EGFRvIII-specific scFv.Int J Cancer 88, no. 6 (December 15, 2000): 962–69. https://doi.org/10.1002/1097-0215(20001215)88:6<962::aid-ijc20>3.0.co;2-u.
Kuan CT, Wikstrand CJ, Archer G, Beers R, Pastan I, Zalutsky MR, et al. Increased binding affinity enhances targeting of glioma xenografts by EGFRvIII-specific scFv. Int J Cancer. 2000 Dec 15;88(6):962–9.
Kuan, C. T., et al. “Increased binding affinity enhances targeting of glioma xenografts by EGFRvIII-specific scFv.Int J Cancer, vol. 88, no. 6, Dec. 2000, pp. 962–69. Pubmed, doi:10.1002/1097-0215(20001215)88:6<962::aid-ijc20>3.0.co;2-u.
Kuan CT, Wikstrand CJ, Archer G, Beers R, Pastan I, Zalutsky MR, Bigner DD. Increased binding affinity enhances targeting of glioma xenografts by EGFRvIII-specific scFv. Int J Cancer. 2000 Dec 15;88(6):962–969.
Journal cover image

Published In

Int J Cancer

DOI

ISSN

0020-7136

Publication Date

December 15, 2000

Volume

88

Issue

6

Start / End Page

962 / 969

Location

United States

Related Subject Headings

  • Transplantation, Heterologous
  • Tissue Distribution
  • Oncology & Carcinogenesis
  • Mice, Nude
  • Mice, Inbred BALB C
  • Mice
  • Iodine Radioisotopes
  • Immunotoxins
  • Immunoglobulin Variable Region
  • Glioma