Literature DB >> 19679884

Development of a Wilms' tumor antigen-specific T-cell receptor for clinical trials: engineered patient's T cells can eliminate autologous leukemia blasts in NOD/SCID mice.

Shao-An Xue1, Liquan Gao, Sharyn Thomas, Daniel P Hart, John Zhao Xue, Roopinder Gillmore, Ralf-Holger Voss, Emma Morris, Hans J Stauss.   

Abstract

BACKGROUND: The Wilms' tumor antigen (WT1) is an attractive target for immunotherapy of leukemia. In the past, we isolated and characterized the specificity and function of a WT1-specific T-cell receptor. The goal of this translational study was to develop a safe and efficient WT1-T-cell receptor retroviral vector for an adoptive immunotherapy trial with engineered T cells. DESIGN AND METHODS: We generated a panel of retroviral constructs containing unmodified or codon-optimized WT1-T-cell receptor alpha and beta genes, linked via internal ribosome entry sites or 2A sequences, with or without an additional inter-chain disulfide bond in the T-cell receptor constant domains. These constructs were functionally analyzed in vitro, and the best one was tested in an autologous primary leukemia model in vivo.
RESULTS: We identified a WT1-T-cell receptor construct that showed optimal tetramer staining, antigen-specific cytokine production and killing activity when introduced into primary human T cells. Fresh CD34(+) cells purified from a patient with leukemia were engrafted into NOD/SCID mice, followed by adoptive immunotherapy with patient's autologous T cells transduced with the WT1-T-cell receptor. This therapeutic treatment evidently decreased leukemia engraftment in mice and resulted in a substantial improvement of leukemia-free survival.
CONCLUSIONS: This is the first report that patient's T cells, engineered to express the WT1-T-cell receptor, can eliminate autologous leukemia progenitor cells in an in vivo model. This study provides a firm basis for the planned WT1-T-cell receptor gene therapy trial in leukemia patients.

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Year:  2009        PMID: 19679884      PMCID: PMC2805729          DOI: 10.3324/haematol.2009.006486

Source DB:  PubMed          Journal:  Haematologica        ISSN: 0390-6078            Impact factor:   9.941


  39 in total

1.  Complete remission in a patient with recurrent acute myeloid leukemia induced by vaccination with WT1 peptide in the absence of hematological or renal toxicity.

Authors:  V Mailänder; C Scheibenbogen; E Thiel; A Letsch; I W Blau; U Keilholz
Journal:  Leukemia       Date:  2004-01       Impact factor: 11.528

2.  The usefulness of monitoring WT1 gene transcripts for the prediction and management of relapse following allogeneic stem cell transplantation in acute type leukemia.

Authors:  Hiroyasu Ogawa; Hiroya Tamaki; Kazuhiro Ikegame; Toshihiro Soma; Manabu Kawakami; Akihiro Tsuboi; Eui Ho Kim; Naoki Hosen; Masaki Murakami; Tatsuya Fujioka; Tomoki Masuda; Yuki Taniguchi; Sumiyuki Nishida; Yusuke Oji; Yoshihiro Oka; Haruo Sugiyama
Journal:  Blood       Date:  2002-10-24       Impact factor: 22.113

3.  Selective elimination of leukemic CD34(+) progenitor cells by cytotoxic T lymphocytes specific for WT1.

Authors:  L Gao; I Bellantuono; A Elsässer; S B Marley; M Y Gordon; J M Goldman; H J Stauss
Journal:  Blood       Date:  2000-04-01       Impact factor: 22.113

4.  Preliminary results of interferon-alpha therapy on woodchuck hepatitis virus-induced hepatocarcinogenesis: possible benefit in female transgenic mice.

Authors:  P Merle; M Chevallier; R Levy; M Maisonnas; O Terradillos; C Trépo; M A Buendia; L Vitvitski-Trépo
Journal:  J Hepatol       Date:  2001-04       Impact factor: 25.083

5.  Human cytotoxic T-lymphocyte responses specific for peptides of the wild-type Wilms' tumor gene (WT1 ) product.

Authors:  Y Oka; O A Elisseeva; A Tsuboi; H Ogawa; H Tamaki; H Li; Y Oji; E H Kim; T Soma; M Asada; K Ueda; E Maruya; H Saji; T Kishimoto; K Udaka; H Sugiyama
Journal:  Immunogenetics       Date:  2000-02       Impact factor: 2.846

6.  Woodchuck hepatitis virus post-transcriptional regulatory element deleted from X protein and promoter sequences enhances retroviral vector titer and expression.

Authors:  A Schambach; J Bohne; C Baum; F G Hermann; L Egerer; D von Laer; T Giroglou
Journal:  Gene Ther       Date:  2006-04       Impact factor: 5.250

7.  Cancer regression and autoimmunity in patients after clonal repopulation with antitumor lymphocytes.

Authors:  Mark E Dudley; John R Wunderlich; Paul F Robbins; James C Yang; Patrick Hwu; Douglas J Schwartzentruber; Suzanne L Topalian; Richard Sherry; Nicholas P Restifo; Amy M Hubicki; Michael R Robinson; Mark Raffeld; Paul Duray; Claudia A Seipp; Linda Rogers-Freezer; Kathleen E Morton; Sharon A Mavroukakis; Donald E White; Steven A Rosenberg
Journal:  Science       Date:  2002-09-19       Impact factor: 47.728

8.  WT1 gene expression: an excellent tool for monitoring minimal residual disease in 70% of acute myeloid leukaemia patients - results from a single-centre study.

Authors:  Mette Østergaard; Lene Hyldahl Olesen; Henrik Hasle; Eigil Kjeldsen; Peter Hokland
Journal:  Br J Haematol       Date:  2004-06       Impact factor: 6.998

Review 9.  WT1 as a universal marker for minimal residual disease detection and quantification in myeloid leukemias and in myelodysplastic syndrome.

Authors:  Daniela Cilloni; Giuseppe Saglio
Journal:  Acta Haematol       Date:  2004       Impact factor: 2.195

10.  Correction of multi-gene deficiency in vivo using a single 'self-cleaving' 2A peptide-based retroviral vector.

Authors:  Andrea L Szymczak; Creg J Workman; Yao Wang; Kate M Vignali; Smaroula Dilioglou; Elio F Vanin; Dario A A Vignali
Journal:  Nat Biotechnol       Date:  2004-04-04       Impact factor: 54.908

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  25 in total

Review 1.  Adoptive transfer of unselected or leukemia-reactive T-cells in the treatment of relapse following allogeneic hematopoietic cell transplantation.

Authors:  Richard J O'Reilly; Tao Dao; Guenther Koehne; David Scheinberg; Ekaterina Doubrovina
Journal:  Semin Immunol       Date:  2010-05-26       Impact factor: 11.130

Review 2.  New Strategies in Engineering T-cell Receptor Gene-Modified T cells to More Effectively Target Malignancies.

Authors:  Thomas M Schmitt; Ingunn M Stromnes; Aude G Chapuis; Philip D Greenberg
Journal:  Clin Cancer Res       Date:  2015-10-13       Impact factor: 12.531

Review 3.  Cellular immunotherapy for malignant gliomas.

Authors:  Yi Lin; Hideho Okada
Journal:  Expert Opin Biol Ther       Date:  2016-07-29       Impact factor: 4.388

4.  T-cell receptor gene transfer for the treatment of leukemia and other tumors.

Authors:  Mirjam H M Heemskerk
Journal:  Haematologica       Date:  2010-01       Impact factor: 9.941

Review 5.  Immune responses and immunotherapeutic interventions in malignant pleural mesothelioma.

Authors:  Adam J Bograd; Kei Suzuki; Eva Vertes; Christos Colovos; Eduardo A Morales; Michel Sadelain; Prasad S Adusumilli
Journal:  Cancer Immunol Immunother       Date:  2011-09-13       Impact factor: 6.968

Review 6.  Augmentation of anti-tumor immunity by adoptive T-cell transfer after allogeneic hematopoietic stem cell transplantation.

Authors:  Marie Bleakley; Cameron J Turtle; Stanley R Riddell
Journal:  Expert Rev Hematol       Date:  2012-08       Impact factor: 2.929

7.  Adiponectin receptor signaling on dendritic cells blunts antitumor immunity.

Authors:  Peng H Tan; Helen E J Tyrrell; Liquan Gao; Danmei Xu; Jianchao Quan; Dipender Gill; Lena Rai; Yunchuan Ding; Gareth Plant; Yuan Chen; John Z Xue; Ashok I Handa; Michael J Greenall; Kenneth Walsh; Shao-An Xue
Journal:  Cancer Res       Date:  2014-09-26       Impact factor: 12.701

8.  Adoptive Immunotherapy after Allogeneic Hematopoietic Progenitor Cell Transplantation: New Perspectives for Transfusion Medicine.

Authors:  Susanne Hofmann; Jochen Greiner
Journal:  Transfus Med Hemother       Date:  2011-05-11       Impact factor: 3.747

Review 9.  Application of adoptive T-cell therapy using tumor antigen-specific T-cell receptor gene transfer for the treatment of human leukemia.

Authors:  Toshiki Ochi; Hiroshi Fujiwara; Masaki Yasukawa
Journal:  J Biomed Biotechnol       Date:  2010-05-05

10.  CpG oligodeoxynucleotides enhance the efficacy of adoptive cell transfer using tumor infiltrating lymphocytes by modifying the Th1 polarization and local infiltration of Th17 cells.

Authors:  Lin Xu; Chunhong Wang; Zhenke Wen; Ya Zhou; Zhongmin Liu; Yongjie Liang; Zengguang Xu; Tao Ren
Journal:  Clin Dev Immunol       Date:  2010-10-20
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