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.
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.
Authors: Stephen E Wright; Kathleen A Rewers-Felkins; Imelda S Quinlin; Catherine A Phillips; Mary Townsend; Ramila Philip; Mark J Dobrzanski; Pamela R Lockwood-Cooke; William Robinson Journal: J Immunother Date: 2012 Feb-Mar Impact factor: 4.456
Authors: Steven Lawrence Rosinski; Brad Stone; Scott S Graves; Deborah H Fuller; Stephen C De Rosa; Gregory A Spies; Gregory J Mize; James T Fuller; Rainer Storb Journal: Transplantation Date: 2015-10 Impact factor: 4.939
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
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