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Monoclonal antibody U36, a suitable candidate for clinical immunotherapy of squamous-cell carcinoma, recognizes a CD44 isoform
- Source :
- Van Hal, N L W, Van Dongen, G A M S, Rood-Knippels, E M C, Van der Valk, P, Snow, G B & Brakenhoff, R H 1996, ' Monoclonal antibody U36, a suitable candidate for clinical immunotherapy of squamous-cell carcinoma, recognizes a CD44 isoform ', International Journal of Cancer, vol. 68, no. 4, pp. 520-527 . https://doi.org/10.1002/(SICI)1097-0215(19961115)68:4<520::AID-IJC19>3.0.CO;2-8, International Journal of Cancer, 68(4), 520-527. Wiley-Liss Inc.
- Publication Year :
- 1996
-
Abstract
- At present, tumor-targeting with monoclonal antibodies (MAbs) is among the most promising novel adjuvant-therapy modalities for the treatment of patients with minimal residual disease of head-and-neck squamous-cell carcinoma (HNSCC). For this purpose we developed MAb U36, recognizing a 200-kDa antigen expressed on the outer cell surface of squamous-cell carcinomas and their normal counterparts. Clinical radioimmunoscintigraphy (RIS) and biodistribution studies have shown that the MAb-U36-defined antigen is a suitable target molecule for antibody-based therapy of head-and-neck cancer. In the present study we further characterized the antigen by cDNA cloning. The cDNA was isolated by expression cloning in COS-7 cells. Sequence analysis and database searching revealed that the MAb-U36-defined antigen is identical to the squamous-cell-specific CD44 splice variant epican. The epitope recognized by MAb U36 was mapped by screening overlapping synthetic peptides of the epican-specific region encoded by exon 7-11 (v3-v7), and appeared to be located in the v6 domain. The applicability of MAb U36 for targeting human tumors of various origin expressing the CD44vb domain is discussed.
Details
- Language :
- English
- ISSN :
- 00207136
- Volume :
- 68
- Issue :
- 4
- Database :
- OpenAIRE
- Journal :
- International Journal of Cancer
- Accession number :
- edsair.doi.dedup.....a3b068d21b7e311c78a705f9d82d7be3
- Full Text :
- https://doi.org/10.1002/(sici)1097-0215(19961115)68:4<520::aid-ijc19>3.0.co;2-8