Literature DB >> 24598452

T-cell therapy using a bank of EBV-specific cytotoxic T cells: lessons from a phase I/II feasibility and safety study.

Géraldine Gallot1, Solène Vollant, Soraya Saïagh, Béatrice Clémenceau, Régine Vivien, Evelyne Cerato, Jean-D Bignon, Christophe Ferrand, Arnaud Jaccard, Stéphane Vigouroux, Sylvain Choquet, Jean-Hugues Dalle, Irène Frachon, Bénédicte Bruno, Mohamad Mothy, Françoise Mechinaud, Véronique Leblond, Noël Milpied, Henri Vié.   

Abstract

We report herein the results we obtained and the limitations we experienced during the production and use of a bank of Epstein-Barr virus (EBV)-transformed human cytotoxic T lymphocytes (EBV-CTLs). To assess the feasibility and toxicity of this strategy, we selected and stored, in liquid nitrogen, 4 billion EBV-CTLs from each of the 13 selected donors. Subsequently, in a multicenter phase I/II study, 11 patients with EBV-associated lymphoma resistant to conventional treatments received 1-3 doses of 5 million EBV-CTLs/kg with 1-3 and 0-4 compatibilities for human leukocyte antigen (HLA)-I and HLA-II, respectively. Except for one event of fever after injection, no immediate or delayed toxicity, no graft versus host disease, and no graft rejection attributable to CTL infusion were observed. Three patients presented complete remission and 1 partial remission after treatment. Considering the clinical options currently available, and the constrains associated with CTL preparation and implementation, we conclude that CTL banks should consist of a reasonably small number of cell lines with documented specificities. This objective could be more easily achieved if the few homozygous donors for the most frequent HLA alleles of the targeted population could be made available for such a project.

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Year:  2014        PMID: 24598452     DOI: 10.1097/CJI.0000000000000031

Source DB:  PubMed          Journal:  J Immunother        ISSN: 1524-9557            Impact factor:   4.456


  21 in total

1.  Feasibility of salvage cord blood transplantation following fludarabine, melphalan and low-dose TBI for graft rejection after hematopoietic stem cell transplantation.

Authors:  K Ishiyama; J Takeda; T Kondo; N Sugimoto; H Kawabata; T Kitano; A Takaori-Kondo
Journal:  Bone Marrow Transplant       Date:  2016-02-15       Impact factor: 5.483

Review 2.  New cell sources for T cell engineering and adoptive immunotherapy.

Authors:  Maria Themeli; Isabelle Rivière; Michel Sadelain
Journal:  Cell Stem Cell       Date:  2015-04-02       Impact factor: 24.633

Review 3.  Epstein-Barr virus lymphoproliferative disease after hematopoietic stem cell transplant.

Authors:  Rayne H Rouce; Chrystal U Louis; Helen E Heslop
Journal:  Curr Opin Hematol       Date:  2014-11       Impact factor: 3.284

4.  Safety and feasibility of virus-specific T cells derived from umbilical cord blood in cord blood transplant recipients.

Authors:  Allistair A Abraham; Tami D John; Michael D Keller; C Russell N Cruz; Baheyeldin Salem; Lauren Roesch; Hao Liu; Fahmida Hoq; Bambi J Grilley; Adrian P Gee; Hema Dave; David A Jacobsohn; Robert A Krance; Elizabeth J Shpall; Caridad A Martinez; Patrick J Hanley; Catherine M Bollard
Journal:  Blood Adv       Date:  2019-07-23

Review 5.  Immunotherapy of lymphomas.

Authors:  Stephen M Ansell; Yi Lin
Journal:  J Clin Invest       Date:  2020-04-01       Impact factor: 14.808

6.  Off-the-shelf EBV-specific T cell immunotherapy for rituximab-refractory EBV-associated lymphoma following transplantation.

Authors:  Susan Prockop; Ekaterina Doubrovina; Stephanie Suser; Glenn Heller; Juliet Barker; Parastoo Dahi; Miguel A Perales; Esperanza Papadopoulos; Craig Sauter; Hugo Castro-Malaspina; Farid Boulad; Kevin J Curran; Sergio Giralt; Boglarka Gyurkocza; Katharine C Hsu; Ann Jakubowski; Alan M Hanash; Nancy A Kernan; Rachel Kobos; Guenther Koehne; Heather Landau; Doris Ponce; Barbara Spitzer; James W Young; Gerald Behr; Mark Dunphy; Sofia Haque; Julie Teruya-Feldstein; Maria Arcila; Christine Moung; Susan Hsu; Aisha Hasan; Richard J O'Reilly
Journal:  J Clin Invest       Date:  2020-02-03       Impact factor: 14.808

Review 7.  Cellular Immunotherapy in Lymphoma: Beyond CART Cells.

Authors:  Mahmoud R Gaballa; Carlos A Ramos
Journal:  Curr Treat Options Oncol       Date:  2020-02-11

Review 8.  Viral-specific T-cell transfer from HSCT donor for the treatment of viral infections or diseases after HSCT.

Authors:  C Qian; Y Wang; L Reppel; M D'aveni; A Campidelli; V Decot; D Bensoussan
Journal:  Bone Marrow Transplant       Date:  2017-10-23       Impact factor: 5.483

Review 9.  Trial Watch: Adoptive cell transfer for oncological indications.

Authors:  Fernando Aranda; Aitziber Buqué; Norma Bloy; Francesca Castoldi; Alexander Eggermont; Isabelle Cremer; Wolf Hervé Fridman; Jitka Fucikova; Jérôme Galon; Radek Spisek; Eric Tartour; Laurence Zitvogel; Guido Kroemer; Lorenzo Galluzzi
Journal:  Oncoimmunology       Date:  2015-05-05       Impact factor: 8.110

Review 10.  Producing proT cells to promote immunotherapies.

Authors:  Jastaranpreet Singh; Juan Carlos Zúñiga-Pflücker
Journal:  Int Immunol       Date:  2018-11-14       Impact factor: 4.823

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