Immunotherapy of myeloid leukaemias
Immunotherapy of myeloid leukaemias
The treatment of myeloid leukaemia has progressed in recent years with the advent of donor leukocyte infusions (DLI), haemopoietic stem cell transplants (HSCTs) and targeted therapies. However, relapse has a high associated morbidity rate and a method for removing diseased cells in first remission, when a minimal residual disease state is achieved and tumour load is low, has the potential to extend remission times and prevent relapse especially when used in combination with conventional treatments. Acute myeloid leukaemia (AML) and myelodysplastic syndrome (MDS) are heterogeneous diseases which lack one common molecular target while chronic myeloid leukaemia (CML) patients have experienced prolonged remissions through the use of targeted therapies which remove BCR-ABL(+) cells effectively in early chronic phase. However, escape mutants have arisen and this therapy has little effectivity in the late chronic phase. Here we review the immune therapies which are close to or in clinical trials for the myeloid leukaemias and describe their potential advantages and disadvantages
myeloid leukaemia, immunotherapy, tumour associated antigens, cancer-testis antigens, SEREX, cDNA microarray
943-957
Guinn, Barbara-Ann
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Mohamedali, Azim
bf5195ae-fe4f-43d7-9dc5-222d2e5776d3
Thomas, N.Shaun B.
0cd2fbef-b152-4ff5-a1bc-a4c7818c00be
Mills, Ken I.
be9c4b93-fda3-40b1-8514-9191652ab8b7
20 December 2006
Guinn, Barbara-Ann
728d28c9-a23d-413a-ba1d-4531005705d7
Mohamedali, Azim
bf5195ae-fe4f-43d7-9dc5-222d2e5776d3
Thomas, N.Shaun B.
0cd2fbef-b152-4ff5-a1bc-a4c7818c00be
Mills, Ken I.
be9c4b93-fda3-40b1-8514-9191652ab8b7
Guinn, Barbara-Ann, Mohamedali, Azim, Thomas, N.Shaun B. and Mills, Ken I.
(2006)
Immunotherapy of myeloid leukaemias.
Cancer Immunology Immunotherapy, 56 (7), .
(doi:10.1007/s00262-006-0267-y).
Abstract
The treatment of myeloid leukaemia has progressed in recent years with the advent of donor leukocyte infusions (DLI), haemopoietic stem cell transplants (HSCTs) and targeted therapies. However, relapse has a high associated morbidity rate and a method for removing diseased cells in first remission, when a minimal residual disease state is achieved and tumour load is low, has the potential to extend remission times and prevent relapse especially when used in combination with conventional treatments. Acute myeloid leukaemia (AML) and myelodysplastic syndrome (MDS) are heterogeneous diseases which lack one common molecular target while chronic myeloid leukaemia (CML) patients have experienced prolonged remissions through the use of targeted therapies which remove BCR-ABL(+) cells effectively in early chronic phase. However, escape mutants have arisen and this therapy has little effectivity in the late chronic phase. Here we review the immune therapies which are close to or in clinical trials for the myeloid leukaemias and describe their potential advantages and disadvantages
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Published date: 20 December 2006
Keywords:
myeloid leukaemia, immunotherapy, tumour associated antigens, cancer-testis antigens, SEREX, cDNA microarray
Identifiers
Local EPrints ID: 71568
URI: http://eprints.soton.ac.uk/id/eprint/71568
ISSN: 0340-7004
PURE UUID: 8b2fb3eb-ce41-4c54-be48-f151d9342344
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Date deposited: 14 Dec 2009
Last modified: 13 Mar 2024 20:33
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Contributors
Author:
Barbara-Ann Guinn
Author:
Azim Mohamedali
Author:
N.Shaun B. Thomas
Author:
Ken I. Mills
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