leukemia
|
0.100 |
Biomarker
|
disease |
BEFREE |
We performed a preclinical validation using a model of CD33<sup>+</sup> AML, and generated iC9 CAR T-cells co-expressing a CAR targeting the AML-associated antigen CD33 and a selectable marker (ΔCD19).ΔCD19 selected (sel.) iC9-CAR.CD33 T-cells were effective in controlling leukemia growth in vitro, and could be partially eliminated (76%) using a chemical inducer of dimerization that activates iC9.
|
30539529 |
2019 |
leukemia
|
0.100 |
Biomarker
|
disease |
BEFREE |
CD33 (siglec-3), a well-known target in leukemia therapy, is an inhibitory sialoadhesin expressed in human leukocytes of the myeloid lineage and some lymphoid subsets, including NK cells.
|
31143782 |
2019 |
leukemia
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Using a human AML cell line (HL-60), we modeled a postremission marrow with minimal residual disease and showed that the transplantation of CD33-ablated HSPCs with CD33-targeted immunotherapy leads to leukemia clearance, without myelosuppression, as demonstrated by the engraftment and recovery of multilineage descendants of CD33-ablated HSPCs.
|
31138698 |
2019 |
leukemia
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Here we present 2 patients with CD33 EML treated with GO.
|
29734213 |
2019 |
leukemia
|
0.100 |
Biomarker
|
disease |
BEFREE |
CD33-deficient cells were impervious to CD33-targeting CAR T cells, allowing for efficient elimination of leukemia without myelotoxicity.
|
29856956 |
2018 |
leukemia
|
0.100 |
Biomarker
|
disease |
BEFREE |
BACKGROUND Leukemia stem cells (LSC) are involved in the incidence, drug resistance, and relapse of leukemia while LSC-related antigen CD33, CD96, and DAPK expression in AML and its prognosis is still unclear.
|
28391288 |
2017 |
leukemia
|
0.100 |
Biomarker
|
disease |
BEFREE |
Dual-specific targeting and elimination were investigated against the B-cell precursor leukemia cell line BV-173 and patient blasts, which were positive for myeloid marker CD33 and B lymphoid marker CD19 exclusively presented on biphenotypic B/myeloid leukemia's.
|
28943878 |
2017 |
leukemia
|
0.100 |
AlteredExpression
|
disease |
BEFREE |
CD33 is variably expressed on leukemia blasts in almost all patients with acute myeloid leukemia (AML) and possibly leukemia stem cells in some.
|
28607471 |
2017 |
leukemia
|
0.100 |
Biomarker
|
disease |
BEFREE |
Challenging ΔCD19 selected inducible Caspase9-CAR.CD33 T-cells with programmed-death-ligand-1 enriched leukemia blasts resulted in significant killing like observed for the programmed-death-ligand-1 negative leukemic blasts fraction.
|
27907031 |
2016 |
leukemia
|
0.100 |
Biomarker
|
disease |
BEFREE |
Furthermore, the CD33-redirected T cells were effective in vivo, preventing the development of leukemia after prophylactic administration and delaying the progression of established disease in mice.
|
25480499 |
2015 |
leukemia
|
0.100 |
Biomarker
|
disease |
BEFREE |
Ectopic expression of SOX7 in K562 and THP-1 cells, as well as primary CD33(+)CD34(+) AML cells, abrogated leukemia engraftment in xenogeneic transplantation.
|
25940713 |
2015 |
leukemia
|
0.100 |
Biomarker
|
disease |
BEFREE |
In vitro experimental (211)At-anti-CD33 antibody therapy of leukaemia cells overcomes cellular resistance seen in vivo against gemtuzumab ozogamicin.
|
20107790 |
2010 |
leukemia
|
0.100 |
Biomarker
|
disease |
BEFREE |
An FLT3-ITD-associated gene-expression signature revealed overexpression of FLT3, homeobox genes (MEIS1, PBX3, HOXB3), and immunotherapeutic tar-gets (WT1, CD33) and underexpression of leukemia-associated (MLLT3, TAL1) and erythropoiesis-associated (GATA3, EPOR, ANK1, HEMGN) genes.
|
20656931 |
2010 |
leukemia
|
0.100 |
Biomarker
|
disease |
BEFREE |
Immunophenotyping has defined an adequate target (CD33) for antibody-directed treatment, although this is not leukemia specific.
|
18024661 |
2007 |
leukemia
|
0.100 |
AlteredExpression
|
disease |
LHGDN |
Overall, our results demonstrate that the expression of CD33 on CD4(+)CD56(+) lineage-negative cells should not exclude the diagnosis of pDC leukemia and underline that pDC-specific markers should be used at diagnosis for CD4(+)CD56(+) malignancies.
|
15388576 |
2005 |
leukemia
|
0.100 |
Biomarker
|
disease |
LHGDN |
Influence of CD33 expression levels and ITIM-dependent internalization on gemtuzumab ozogamicin-induced cytotoxicity.
|
15454492 |
2005 |
leukemia
|
0.100 |
Biomarker
|
disease |
LHGDN |
Ligation of the leukemia-associated antigen CD33 by anti-CD33 monoclonal antibody (mAb) also results in signaling events that induce a downregulation of cell growth.
|
15676214 |
2005 |
leukemia
|
0.100 |
Biomarker
|
disease |
BEFREE |
Two cases of CD56+CD33+ leukemia/lymphoma are reported.
|
15270596 |
2004 |
leukemia
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
In addition, immunophenotypic analysis revealed the coexpression of the CD33 and CD7 antigens on common ALL blasts, in accordance with other reported cases that displayed a predominant biphenotypic leukemia profile.
|
12810259 |
2003 |
leukemia
|
0.100 |
Biomarker
|
disease |
BEFREE |
The patient was an adult male diagnosed with ALL(L2), Cell marker studies showed positivity for CD3, CD7, CD13 and CD33, so the phenotypic diagnosis was determined to be biphenotypic leukemia.
|
11342322 |
2000 |
leukemia
|
0.100 |
Biomarker
|
disease |
BEFREE |
NALM-29 cells display biphenotypic characteristics: expression of the intracellular enzyme myeloperoxidase at the mRNA and protein level and cell surface positivity for CD19, CD10, CD13, CD33 and HLA-DR. NALM-29 fulfills EGIL criteria as B-cell precursor (BCP) leukemia B-II type.
|
10456671 |
1999 |
leukemia
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
However, donors homozygous for this allele could be used to generate cytotoxic T cells against the frequent CD33 allele, for adoptive therapy of leukaemia.
|
9753070 |
1998 |
leukemia
|
0.100 |
AlteredExpression
|
disease |
BEFREE |
Our results suggest that the leukemia with inv(3)(q21q26) represents a new cytogenetic-clinicopathologic subtype, characterized by 1) abnormal megakaryopoiesis and multiple hematopoietic lineage involvement; 2) an antecedent MDS; 3) poor response to conventional chemotherapy; and 4) expression of CD7, CD34, CD38, HLA-DR, CD13, and CD33 antigens.
|
9209472 |
1997 |
leukemia
|
0.100 |
Biomarker
|
disease |
BEFREE |
It is therefore intriguing from a biological standpoint why the supposedly early antigens (CD33 and CD13) remain unexpressed; this may represent an example of 'asynchronous differentiation' in leukaemia.
|
1382546 |
1992 |