Literature DB >> 27289360

Current status of ex vivo gene therapy for hematological disorders: a review of clinical trials in Japan around the world.

Kenzaburo Tani1.   

Abstract

Gene therapies are classified into two major categories, namely, in vivo and ex vivo. Clinical trials of human gene therapy began with the ex vivo techniques. Based on the initial successes of gene-therapy clinical trials, these approaches have spread worldwide. The number of gene therapy trials approved worldwide increased gradually starting in 1989, reaching 116 protocols per year in 1999, and a total of 2210 protocols had been approved by 2015. Accumulating clinical evidence has demonstrated the safety and benefits of several types of gene therapy, with the exception of serious adverse events in several clinical trials. These painful experiences were translated backward to basic science, resulting in the development of several new technologies that have influenced the recent development of ex vivo gene therapy in this field. To date, six gene therapies have been approved in a limited number of countries worldwide. In Japan, clinical trials of gene therapy have developed under the strong influence of trials in the US and Europe. Since the initial stages, 50 clinical trials have been approved by the Japanese government. In this review, the history and current status of clinical trials of ex vivo gene therapy for hematological disorders are introduced and discussed.

Entities:  

Keywords:  Adenosine deaminase deficiency; Chronic granulomatous disease; Leukemia cell vaccine; Severe combined immune deficiency; Wiskott-Aldrich syndrome

Mesh:

Year:  2016        PMID: 27289360     DOI: 10.1007/s12185-016-2030-2

Source DB:  PubMed          Journal:  Int J Hematol        ISSN: 0925-5710            Impact factor:   2.490


  85 in total

Review 1.  Gene therapy for monogenic disorders of the bone marrow.

Authors:  Sujal Ghosh; Adrian J Thrasher; H Bobby Gaspar
Journal:  Br J Haematol       Date:  2015-06-05       Impact factor: 6.998

2.  New Japanese initiatives on stem cell therapies.

Authors:  Kenji Konomi; Morikuni Tobita; Kenichi Kimura; Daisaku Sato
Journal:  Cell Stem Cell       Date:  2015-04-02       Impact factor: 24.633

3.  Inducible caspase-9 suicide gene controls adverse effects from alloreplete T cells after haploidentical stem cell transplantation.

Authors:  Xiaoou Zhou; Gianpietro Dotti; Robert A Krance; Caridad A Martinez; Swati Naik; Rammurti T Kamble; April G Durett; Olga Dakhova; Barbara Savoldo; Antonio Di Stasi; David M Spencer; Yu-Feng Lin; Hao Liu; Bambi J Grilley; Adrian P Gee; Cliona M Rooney; Helen E Heslop; Malcolm K Brenner
Journal:  Blood       Date:  2015-05-14       Impact factor: 22.113

Review 4.  Adoptive T-cell therapy for hematological malignancies using T cells gene-modified to express tumor antigen-specific receptors.

Authors:  Hiroshi Fujiwara
Journal:  Int J Hematol       Date:  2013-12-19       Impact factor: 2.490

5.  Multicenter phase I study of repeated intratumoral delivery of adenoviral p53 in patients with advanced non-small-cell lung cancer.

Authors:  Toshiyoshi Fujiwara; Noriaki Tanaka; Susumu Kanazawa; Shoichiro Ohtani; Yasuo Saijo; Toshihiro Nukiwa; Kunihiko Yoshimura; Tetsuo Sato; Yoshikatsu Eto; Sunil Chada; Haruhiko Nakamura; Harubumi Kato
Journal:  J Clin Oncol       Date:  2006-02-27       Impact factor: 44.544

6.  Transfusion independence and HMGA2 activation after gene therapy of human β-thalassaemia.

Authors:  Marina Cavazzana-Calvo; Emmanuel Payen; Olivier Negre; Gary Wang; Kathleen Hehir; Floriane Fusil; Julian Down; Maria Denaro; Troy Brady; Karen Westerman; Resy Cavallesco; Beatrix Gillet-Legrand; Laure Caccavelli; Riccardo Sgarra; Leila Maouche-Chrétien; Françoise Bernaudin; Robert Girot; Ronald Dorazio; Geert-Jan Mulder; Axel Polack; Arthur Bank; Jean Soulier; Jérôme Larghero; Nabil Kabbara; Bruno Dalle; Bernard Gourmel; Gérard Socie; Stany Chrétien; Nathalie Cartier; Patrick Aubourg; Alain Fischer; Kenneth Cornetta; Frédéric Galacteros; Yves Beuzard; Eliane Gluckman; Frederick Bushman; Salima Hacein-Bey-Abina; Philippe Leboulch
Journal:  Nature       Date:  2010-09-16       Impact factor: 49.962

7.  Correction of X-linked chronic granulomatous disease by gene therapy, augmented by insertional activation of MDS1-EVI1, PRDM16 or SETBP1.

Authors:  Marion G Ott; Manfred Schmidt; Kerstin Schwarzwaelder; Stefan Stein; Ulrich Siler; Ulrike Koehl; Hanno Glimm; Klaus Kühlcke; Andrea Schilz; Hana Kunkel; Sonja Naundorf; Andrea Brinkmann; Annette Deichmann; Marlene Fischer; Claudia Ball; Ingo Pilz; Cynthia Dunbar; Yang Du; Nancy A Jenkins; Neal G Copeland; Ursula Lüthi; Moustapha Hassan; Adrian J Thrasher; Dieter Hoelzer; Christof von Kalle; Reinhard Seger; Manuel Grez
Journal:  Nat Med       Date:  2006-04-02       Impact factor: 53.440

8.  Biologic activity of irradiated, autologous, GM-CSF-secreting leukemia cell vaccines early after allogeneic stem cell transplantation.

Authors:  Vincent T Ho; Matthew Vanneman; Haesook Kim; Tetsuro Sasada; Yoon Joong Kang; Mildred Pasek; Corey Cutler; John Koreth; Edwin Alyea; Stefanie Sarantopoulos; Joseph H Antin; Jerome Ritz; Christine Canning; Jeffery Kutok; Martin C Mihm; Glenn Dranoff; Robert Soiffer
Journal:  Proc Natl Acad Sci U S A       Date:  2009-08-26       Impact factor: 11.205

9.  Gene therapy improves immune function in preadolescents with X-linked severe combined immunodeficiency.

Authors:  Javier Chinen; Joie Davis; Suk See De Ravin; Beverly N Hay; Amy P Hsu; Gilda F Linton; Nora Naumann; Effie Y H Nomicos; Christopher Silvin; Jean Ulrick; Narda L Whiting-Theobald; Harry L Malech; Jennifer M Puck
Journal:  Blood       Date:  2007-03-16       Impact factor: 22.113

Review 10.  Gene therapy for inherited immunodeficiency.

Authors:  Fabien Touzot; Salima Hacein-Bey-Abina; Alain Fischer; Marina Cavazzana
Journal:  Expert Opin Biol Ther       Date:  2014-03-08       Impact factor: 4.388

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  2 in total

Review 1.  Development and clinical translation of ex vivo gene therapy.

Authors:  Xiaomo Wu; Xiaorong He; Fahui Liu; Xiaochang Jiang; Ping Wang; Jinyan Zhang; Ju Jiang
Journal:  Comput Struct Biotechnol J       Date:  2022-06-11       Impact factor: 6.155

2.  Improving the Safety of Mesenchymal Stem Cell-Based Ex Vivo Therapy Using Herpes Simplex Virus Thymidine Kinase.

Authors:  Narayan Bashyal; Tae-Young Lee; Da-Young Chang; Jin-Hwa Jung; Min Gyeong Kim; Rakshya Acharya; Sung-Soo Kim; Il-Hoan Oh; Haeyoung Suh-Kim
Journal:  Mol Cells       Date:  2022-03-21       Impact factor: 4.250

  2 in total

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