Literature DB >> 15782542

Effective tumor targeting: strategies for the delivery of Armed Antibodies.

Glen C MacDonald1, Nick Glover.   

Abstract

It has long been realized that the presence of tumor-associated antigens offers an excellent opportunity for targeted cancer therapy and hence an improved clinical benefit for cancer patients. Advances in the field of antibody engineering as well as the characterization of toxins, such as diphtheria toxin and Pseudomonas exotoxin A, have enabled the routine construction of recombinant immunotoxins, which we have termed Armed Antibodies. The selective toxicity and mechanism of action of these molecules could potentially provide an excellent clinical alternative to conventional anticancer agents which have many unacceptable side effects. Although considerable clinical success has been achieved using immunotoxin therapy, particularly for B-cell malignancies, the treatment of solid tumors remains highly challenging. To successfully treat solid tumors that are not amenable to local therapy, immunotoxins must be designed to permit repeat systemic administration. This review outlines some of the strategies currently being employed in the design of the Viventia Biotech Inc Armed Antibodies to minimize the development of immunogenicity and to remove the potential for toxicity in non-target tissues.

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Year:  2005        PMID: 15782542

Source DB:  PubMed          Journal:  Curr Opin Drug Discov Devel        ISSN: 1367-6733


  7 in total

1.  A phase I clinical study of intratumorally administered VB4-845, an anti-epithelial cell adhesion molecule recombinant fusion protein, in patients with squamous cell carcinoma of the head and neck.

Authors:  G C MacDonald; M Rasamoelisolo; J Entwistle; W Cuthbert; M Kowalski; Maureen A Spearman; N Glover
Journal:  Med Oncol       Date:  2008-10-28       Impact factor: 3.064

Review 2.  Addressing the Immunogenicity of the Cargo and of the Targeting Antibodies with a Focus on Demmunized Bacterial Toxins and on Antibody-Targeted Human Effector Proteins.

Authors:  Yehudit Grinberg; Itai Benhar
Journal:  Biomedicines       Date:  2017-06-02

Review 3.  Strategies to Improve the Clinical Utility of Saporin-Based Targeted Toxins.

Authors:  Francesco Giansanti; David J Flavell; Francesco Angelucci; Maria Serena Fabbrini; Rodolfo Ippoliti
Journal:  Toxins (Basel)       Date:  2018-02-13       Impact factor: 4.546

4.  Aptamer-Driven Toxin Gene Delivery in U87 Model Glioblastoma Cells.

Authors:  Luana di Leandro; Francesco Giansanti; Sabrina Mei; Sara Ponziani; Martina Colasante; Matteo Ardini; Francesco Angelucci; Giuseppina Pitari; Michele d'Angelo; Annamaria Cimini; Maria Serena Fabbrini; Rodolfo Ippoliti
Journal:  Front Pharmacol       Date:  2021-04-15       Impact factor: 5.810

5.  A phase I clinical study of VB4-845: weekly intratumoral administration of an anti-EpCAM recombinant fusion protein in patients with squamous cell carcinoma of the head and neck.

Authors:  Glen C MacDonald; Michèle Rasamoelisolo; Joycelyn Entwistle; Jeannick Cizeau; Denis Bosc; Wendy Cuthbert; Mark Kowalski; Maureen Spearman; Nick Glover
Journal:  Drug Des Devel Ther       Date:  2009-02-06       Impact factor: 4.162

6.  A bispecific diabody directed against prostate-specific membrane antigen and CD3 induces T-cell mediated lysis of prostate cancer cells.

Authors:  P Bühler; P Wolf; D Gierschner; I Schaber; A Katzenwadel; W Schultze-Seemann; U Wetterauer; M Tacke; M Swamy; W W A Schamel; U Elsässer-Beile
Journal:  Cancer Immunol Immunother       Date:  2007-06-20       Impact factor: 6.968

7.  Potent anti-tumor activity of CD45RA-targeting Hm3A4-Ranpirnase against myeloid lineage leukemias.

Authors:  Sisi Li; Zhujun Wang; Xiaoping Guo; Ping Chen; Yongmin Tang
Journal:  Bioengineered       Date:  2022-04       Impact factor: 6.832

  7 in total

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