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New insights into antigen specific immunotherapy for chronic myeloid leukemia

Chronic myeloid leukemia (CML) is a stem cell disease in which BCR/ABL plays an important role as an oncoprotein and a molecular and immunogenic target. Despite the success of targeted therapy using tyrosine kinase inhibitors (TKIs), CML remains largely incurable, most likely due to the treatment re...

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Detalles Bibliográficos
Autores principales: Li, Yangqiu, Lin, Chen, Schmidt, Christian A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3538626/
https://www.ncbi.nlm.nih.gov/pubmed/23241263
http://dx.doi.org/10.1186/1475-2867-12-52
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author Li, Yangqiu
Lin, Chen
Schmidt, Christian A
author_facet Li, Yangqiu
Lin, Chen
Schmidt, Christian A
author_sort Li, Yangqiu
collection PubMed
description Chronic myeloid leukemia (CML) is a stem cell disease in which BCR/ABL plays an important role as an oncoprotein and a molecular and immunogenic target. Despite the success of targeted therapy using tyrosine kinase inhibitors (TKIs), CML remains largely incurable, most likely due to the treatment resistance of leukemic stem cells. Several immunotherapies have been developed for CML in different stages and relapse after allogeneic stem cell transplantation. In the this review, several specific immunotherapeutic approaches for CML, including vaccination and adoptive cellular immunotherapy, are discussed along with results from clinical trials, and the value of such immunotherapies in the era of imatinib and leukemia-associated antigens (LAAs), which are capable of inducing specific T cell responses and are appropriate target structures for the immunological targeting of CML cells, are also summarized.
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spelling pubmed-35386262013-01-10 New insights into antigen specific immunotherapy for chronic myeloid leukemia Li, Yangqiu Lin, Chen Schmidt, Christian A Cancer Cell Int Review Chronic myeloid leukemia (CML) is a stem cell disease in which BCR/ABL plays an important role as an oncoprotein and a molecular and immunogenic target. Despite the success of targeted therapy using tyrosine kinase inhibitors (TKIs), CML remains largely incurable, most likely due to the treatment resistance of leukemic stem cells. Several immunotherapies have been developed for CML in different stages and relapse after allogeneic stem cell transplantation. In the this review, several specific immunotherapeutic approaches for CML, including vaccination and adoptive cellular immunotherapy, are discussed along with results from clinical trials, and the value of such immunotherapies in the era of imatinib and leukemia-associated antigens (LAAs), which are capable of inducing specific T cell responses and are appropriate target structures for the immunological targeting of CML cells, are also summarized. BioMed Central 2012-12-15 /pmc/articles/PMC3538626/ /pubmed/23241263 http://dx.doi.org/10.1186/1475-2867-12-52 Text en Copyright ©2012 Li et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Li, Yangqiu
Lin, Chen
Schmidt, Christian A
New insights into antigen specific immunotherapy for chronic myeloid leukemia
title New insights into antigen specific immunotherapy for chronic myeloid leukemia
title_full New insights into antigen specific immunotherapy for chronic myeloid leukemia
title_fullStr New insights into antigen specific immunotherapy for chronic myeloid leukemia
title_full_unstemmed New insights into antigen specific immunotherapy for chronic myeloid leukemia
title_short New insights into antigen specific immunotherapy for chronic myeloid leukemia
title_sort new insights into antigen specific immunotherapy for chronic myeloid leukemia
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3538626/
https://www.ncbi.nlm.nih.gov/pubmed/23241263
http://dx.doi.org/10.1186/1475-2867-12-52
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