Literature DB >> 26443804

Recombinant Immunotoxin with T-cell Epitope Mutations That Greatly Reduce Immunogenicity for Treatment of Mesothelin-Expressing Tumors.

Ronit Mazor1, Jingli Zhang1, Laiman Xiang1, Selamawit Addissie1, Prince Awuah1, Richard Beers1, Raffit Hassan1, Ira Pastan2.   

Abstract

SS1P is a recombinant immunotoxin (RIT) that targets mesothelin. It consists of an antimesothelin Fv fused to a portion of Pseudomonas exotoxin A. In clinical studies, it has produced dramatic responses in patients with advanced mesothelioma, when combined with immunosuppressive therapy so that several treatment cycles could be given. Otherwise its activity is limited by its immunogenicity. In this work, we describe the development and characterization of LMB-T20, a highly potent RIT targeted at mesothelin-expressing cancers with low immunogenicity due to removal of its eight T-cell epitopes. LMB-T20 was more active than SS1P when tested on four different mesothelin-expressing cell lines as well as on cells obtained from patients with mesothelioma. It also has potent antitumor activity in mice, and has reduced immunogenicity as measured by cytokine secretion assays. In conclusion, LMB-T20 is a favorable candidate for evaluation in clinical trials due to its reduced immunogenicity and excellent activity. ©2015 American Association for Cancer Research.

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Year:  2015        PMID: 26443804      PMCID: PMC4674367          DOI: 10.1158/1535-7163.MCT-15-0532

Source DB:  PubMed          Journal:  Mol Cancer Ther        ISSN: 1535-7163            Impact factor:   6.009


  30 in total

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6.  Humoral immune response to mesothelin in mesothelioma and ovarian cancer patients.

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Review 7.  Immunogenicity of therapeutic recombinant immunotoxins.

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10.  Improving the In Vivo Efficacy of an Anti-Tac (CD25) Immunotoxin by Pseudomonas Exotoxin A Domain II Engineering.

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