Cargando…
New targets for therapy: antigen identification in adults with B-cell acute lymphoblastic leukaemia
Acute lymphoblastic leukaemia (ALL) in adults is a rare and difficult-to-treat cancer that is characterised by excess lymphoblasts in the bone marrow. Although many patients achieve remission with chemotherapy, relapse rates are high and the associated impact on survival devastating. Most patients r...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7183504/ https://www.ncbi.nlm.nih.gov/pubmed/31970440 http://dx.doi.org/10.1007/s00262-020-02484-0 |
_version_ | 1783526427404009472 |
---|---|
author | Jordaens, Stephanie Cooksey, Leah Freire Boullosa, Laurie Van Tendeloo, Viggo Smits, Evelien Mills, Ken I. Orchard, Kim H. Guinn, Barbara-ann |
author_facet | Jordaens, Stephanie Cooksey, Leah Freire Boullosa, Laurie Van Tendeloo, Viggo Smits, Evelien Mills, Ken I. Orchard, Kim H. Guinn, Barbara-ann |
author_sort | Jordaens, Stephanie |
collection | PubMed |
description | Acute lymphoblastic leukaemia (ALL) in adults is a rare and difficult-to-treat cancer that is characterised by excess lymphoblasts in the bone marrow. Although many patients achieve remission with chemotherapy, relapse rates are high and the associated impact on survival devastating. Most patients receive chemotherapy and for those whose overall fitness supports it, the most effective treatment to date is allogeneic stem cell transplant that can improve overall survival rates in part due to a ‘graft-versus-leukaemia’ effect. However, due to the rarity of this disease, and the availability of mature B-cell antigens on the cell surface, few new cancer antigens have been identified in adult B-ALL that could act as targets to remove residual disease in first remission or provide alternative targets for escape variants if and when current immunotherapy strategies fail. We have used RT-PCR analysis, literature searches, antibody-specific profiling and gene expression microarray analysis to identify and prioritise antigens as novel targets for the treatment of adult B-ALL. |
format | Online Article Text |
id | pubmed-7183504 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-71835042020-04-29 New targets for therapy: antigen identification in adults with B-cell acute lymphoblastic leukaemia Jordaens, Stephanie Cooksey, Leah Freire Boullosa, Laurie Van Tendeloo, Viggo Smits, Evelien Mills, Ken I. Orchard, Kim H. Guinn, Barbara-ann Cancer Immunol Immunother Focussed Research Review Acute lymphoblastic leukaemia (ALL) in adults is a rare and difficult-to-treat cancer that is characterised by excess lymphoblasts in the bone marrow. Although many patients achieve remission with chemotherapy, relapse rates are high and the associated impact on survival devastating. Most patients receive chemotherapy and for those whose overall fitness supports it, the most effective treatment to date is allogeneic stem cell transplant that can improve overall survival rates in part due to a ‘graft-versus-leukaemia’ effect. However, due to the rarity of this disease, and the availability of mature B-cell antigens on the cell surface, few new cancer antigens have been identified in adult B-ALL that could act as targets to remove residual disease in first remission or provide alternative targets for escape variants if and when current immunotherapy strategies fail. We have used RT-PCR analysis, literature searches, antibody-specific profiling and gene expression microarray analysis to identify and prioritise antigens as novel targets for the treatment of adult B-ALL. Springer Berlin Heidelberg 2020-01-22 2020 /pmc/articles/PMC7183504/ /pubmed/31970440 http://dx.doi.org/10.1007/s00262-020-02484-0 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Focussed Research Review Jordaens, Stephanie Cooksey, Leah Freire Boullosa, Laurie Van Tendeloo, Viggo Smits, Evelien Mills, Ken I. Orchard, Kim H. Guinn, Barbara-ann New targets for therapy: antigen identification in adults with B-cell acute lymphoblastic leukaemia |
title | New targets for therapy: antigen identification in adults with B-cell acute lymphoblastic leukaemia |
title_full | New targets for therapy: antigen identification in adults with B-cell acute lymphoblastic leukaemia |
title_fullStr | New targets for therapy: antigen identification in adults with B-cell acute lymphoblastic leukaemia |
title_full_unstemmed | New targets for therapy: antigen identification in adults with B-cell acute lymphoblastic leukaemia |
title_short | New targets for therapy: antigen identification in adults with B-cell acute lymphoblastic leukaemia |
title_sort | new targets for therapy: antigen identification in adults with b-cell acute lymphoblastic leukaemia |
topic | Focussed Research Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7183504/ https://www.ncbi.nlm.nih.gov/pubmed/31970440 http://dx.doi.org/10.1007/s00262-020-02484-0 |
work_keys_str_mv | AT jordaensstephanie newtargetsfortherapyantigenidentificationinadultswithbcellacutelymphoblasticleukaemia AT cookseyleah newtargetsfortherapyantigenidentificationinadultswithbcellacutelymphoblasticleukaemia AT freireboullosalaurie newtargetsfortherapyantigenidentificationinadultswithbcellacutelymphoblasticleukaemia AT vantendelooviggo newtargetsfortherapyantigenidentificationinadultswithbcellacutelymphoblasticleukaemia AT smitsevelien newtargetsfortherapyantigenidentificationinadultswithbcellacutelymphoblasticleukaemia AT millskeni newtargetsfortherapyantigenidentificationinadultswithbcellacutelymphoblasticleukaemia AT orchardkimh newtargetsfortherapyantigenidentificationinadultswithbcellacutelymphoblasticleukaemia AT guinnbarbaraann newtargetsfortherapyantigenidentificationinadultswithbcellacutelymphoblasticleukaemia |