Literature DB >> 15268678

Recombinant immunotoxins for the treatment of haematological malignancies.

Robert J Kreitman1.   

Abstract

Recombinant immunotoxins are fusion proteins which contain a ligand derived from the immune system fused to a toxin. The protein toxin is truncated to delete its binding domain, allowing selective ligand-directed binding. Growth factor fusion toxins are often considered immunotoxins. One of these molecules, containing the truncated diphtheria toxin and human IL-2 (Ontak), Ligand Pharmaceuticals), has been approved for the treatment of cutaneous T-cell lymphoma. Recombinant immunotoxins have also been produced containing the variable domains (Fv fragment) of monoclonal antibodies fused to toxins. These agents are relatively versatile with respect to the range of antigens possible. Several of these recombinant immunotoxins have showed clinical effectiveness in Phase I testing against haematological malignancies. One of these molecules, BL22, targets CD22 on hairy-cell leukaemia and has enabled patients to achieve complete remissions despite previous treatment and resistance to chemotherapy.

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Year:  2004        PMID: 15268678     DOI: 10.1517/14712598.4.7.1115

Source DB:  PubMed          Journal:  Expert Opin Biol Ther        ISSN: 1471-2598            Impact factor:   4.388


  6 in total

Review 1.  Thrombotic microangiopathy with targeted cancer agents.

Authors:  John A Blake-Haskins; Robert J Lechleider; Robert J Kreitman
Journal:  Clin Cancer Res       Date:  2011-08-03       Impact factor: 12.531

2.  Selective elimination of human regulatory T lymphocytes in vitro with the recombinant immunotoxin LMB-2.

Authors:  Peter Attia; Daniel J Powell; Ajay V Maker; Robert J Kreitman; Ira Pastan; Steven A Rosenberg
Journal:  J Immunother       Date:  2006 Mar-Apr       Impact factor: 4.456

3.  Partial reduction of human FOXP3+ CD4 T cells in vivo after CD25-directed recombinant immunotoxin administration.

Authors:  Daniel J Powell; Peter Attia; Victor Ghetie; John Schindler; Ellen S Vitetta; Steven A Rosenberg
Journal:  J Immunother       Date:  2008 Feb-Mar       Impact factor: 4.456

Review 4.  Toxin-based therapeutic approaches.

Authors:  Assaf Shapira; Itai Benhar
Journal:  Toxins (Basel)       Date:  2010-10-28       Impact factor: 4.546

5.  The efficacy of NP11-4-derived immunotoxin scFv-artesunate in reducing hepatic fibrosis induced by Schistosoma japonicum in mice.

Authors:  Hong Li; Chunyan Gu; Yongya Ren; Yang Dai; Xiaojuan Zhu; Jing Xu; Yuhua Li; Zhenning Qiu; Jin Zhu; Yinchang Zhu; Xiaohong Guan; Zhenqing Feng
Journal:  J Biomed Res       Date:  2011-03

6.  CCR4-expressing T cell tumors can be specifically controlled via delivery of toxins to chemokine receptors.

Authors:  Dolgor Baatar; Purevdorj Olkhanud; Dianne Newton; Kenya Sumitomo; Arya Biragyn
Journal:  J Immunol       Date:  2007-08-01       Impact factor: 5.426

  6 in total

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