Literature DB >> 17229638

Phase I/II feasibility study evaluating the generation of leukemia-reactive cytotoxic T lymphocyte lines for treatment of patients with relapsed leukemia after allogeneic stem cell transplantation.

Erik Marijt1, Amon Wafelman, Menno van der Hoorn, Cornelis van Bergen, Rian Bongaerts, Simone van Luxemburg-Heijs, Joost van den Muijsenberg, Judith Olde Wolbers, Nicole van der Werff, Roel Willemze, Frederik Falkenburg.   

Abstract

BACKGROUND AND OBJECTIVES: Graft-versus-host-disease may be avoided and the likelihood of a graft-versus-leukemia reaction increased by infusion of in vitro generated, leukemia-reactive, cytotoxic T lymphocyte (CTL) lines as treatment for patients with relapsed leukemia after allogeneic stem cell transplantation, instead of donor lymphocyte infusion. The aim of this study phase I/II study was to assess the feasibility of large-scale in vitro generation of leukemia-reactive CTL for clinical use. DESIGN AND METHODS: Using a modified limiting dilution culture system donor T cells were stimulated with HLA-identical leukemic antigen presenting cells. Feasibility experiments demonstrated that in 16 of 27 donor-recipient pairs tested a CTL line could be generated. Twelve of these 16 patients developed a relapse and for 11 of these 12 patients a CTL line was generated under Good Manufacturing Practice conditions.
RESULTS: The CTL lines showed moderate to high cytotoxic activity against original recipient leukemic cells in vitro. Eight patients with a relapse received from one to seven CTL lines. One patient entered a complete remission after CTL infusion only, one entered a complete remission after combined CTL infusion and donor lymphocyte infusion, two patients had temporarily stable disease, and in four patients no response was observed. INTERPRETATION AND
CONCLUSIONS: Although the current procedure to generate these CTL lines is feasible, the strategy is logistically complex and time-consuming, and needs further improvement. Key words: cellular immunotherapy, CTL, leukemia, allogeneic stem cell transplantation.

Entities:  

Mesh:

Year:  2007        PMID: 17229638     DOI: 10.3324/haematol.10433

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


  11 in total

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Review 2.  T cell therapy in allogeneic stem cell transplantation.

Authors:  J H Frederik Falkenburg; Helen E Heslop; A John Barrett
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4.  Generation and administration of HA-1-specific T-cell lines for the treatment of patients with relapsed leukemia after allogeneic stem cell transplantation: a pilot study.

Authors:  Pauline Meij; Inge Jedema; Menno A W G van der Hoorn; Rian Bongaerts; Linda Cox; Amon R Wafelman; Erik W A Marijt; Roel Willemze; J H Frederik Falkenburg
Journal:  Haematologica       Date:  2012-04-17       Impact factor: 9.941

Review 5.  Immunomodulation in the treatment of haematological malignancies.

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7.  Cellular therapy following allogeneic stem-cell transplantation.

Authors:  Alison Rager; David L Porter
Journal:  Ther Adv Hematol       Date:  2011-12

Review 8.  Cell-based strategies to manage leukemia relapse: efficacy and feasibility of immunotherapy approaches.

Authors:  A Rambaldi; E Biagi; C Bonini; A Biondi; M Introna
Journal:  Leukemia       Date:  2014-06-12       Impact factor: 11.528

9.  Depletion of endogenous tumor-associated regulatory T cells improves the efficacy of adoptive cytotoxic T-cell immunotherapy in murine acute myeloid leukemia.

Authors:  Qing Zhou; Christoph Bucher; Meghan E Munger; Steven L Highfill; Jakub Tolar; David H Munn; Bruce L Levine; Megan Riddle; Carl H June; Daniel A Vallera; Brenda J Weigel; Bruce R Blazar
Journal:  Blood       Date:  2009-09-01       Impact factor: 22.113

10.  Improving TCR Gene Therapy for Treatment of Haematological Malignancies.

Authors:  Emma Nicholson; Sara Ghorashian; Hans Stauss
Journal:  Adv Hematol       Date:  2012-01-26
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