TY - JOUR
T1 - New targets for therapy antigen identification in adults with B-cell acute lymphoblastic leukaemia
AU - Jordaens, Stephanie
AU - Cooksey, Leah
AU - Freire Boullosa, Laurie
AU - Van Tendeloo, Viggo
AU - Smits, Evelien
AU - Mills, Ken I
AU - Orchard, Kim H
AU - Guinn, Barbara-Ann
PY - 2020/1/22
Y1 - 2020/1/22
N2 - 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.
AB - 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.
U2 - 10.1007/s00262-020-02484-0
DO - 10.1007/s00262-020-02484-0
M3 - Review article
C2 - 31970440
SN - 0340-7004
JO - Cancer immunology, immunotherapy : CII
JF - Cancer immunology, immunotherapy : CII
ER -