Donor-derived b2a2-specific T cells for immunotherapy of patients with chronic myeloid leukemia


Autoria(s): Crough, T; Nieda, M; Morton, J; Bashford, J; Durrant, S; Nicol, AJ
Contribuinte(s)

S. A. Rosenberg

Data(s)

01/01/2002

Resumo

The BCR-ABL fusion proteins, b2a2 and b3a2, are potential targets for a beneficial graft-versus-leukemia (GVL) effect after allogeneic stem cell transplantation for chronic myeloid leukemia (CML). This study demonstrates that CD4(+) T cells specific to the b2a2 peptide can be generated from a normal allogeneic stem cell transplant donor after stimulation with monocyte-derived dendritic cells (Mo-DC) using culture conditions applicable to clinical use. Stimulation of donor T-cell enriched mononuclear cells (MNC) with b2a2-pulsed Mo-DC produced approximately 3 x 10(9) b2a2-specific CD4(+) T cells. The CD4(+) T cells were HLA-DR7 restricted. These results confirm that the generation of donor derived b2a2-specific T cells for clinical use is feasible and warrants clinical testing after stem cell transplantation.

Identificador

http://espace.library.uq.edu.au/view/UQ:63974

Idioma(s)

eng

Publicador

Lippincott Williams & Wilkins

Palavras-Chave #Oncology #Immunology #Medicine, Research & Experimental #B2a2 #Chronic Myeloid Leukemia #Dendritic Cell #Immunotherapy #T Cells #Chronic Myelogenous Leukemia #Bone-marrow Transplantation #Polymerase Chain-reaction #Versus-host Disease #Dendritic Cells #Selective Depletion #Peripheral-blood #Bcr #Lymphocytes #Immunity #C1 #320206 Tumor Immunology #730108 Cancer and related disorders
Tipo

Journal Article