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The Src/ABL kinase inhibitor dasatinib (BMS-354825) inhibits function of normal human T-lymphocytes in vitro
- Source :
- Clinical Immunology. 127:330-339
- Publication Year :
- 2008
- Publisher :
- Elsevier BV, 2008.
-
Abstract
- Dasatinib (BMS-354825) is a Src/ABL tyrosine kinase inhibitor currently approved for the treatment of chronic myeloid leukemia. Dasatinib has increased potency against ABL compared to the current therapy imatinib, and is effective in many cases where disease is resistant to imatinib. Dasatinib also inhibits many Src-family tyrosine kinases. We have demonstrated in this study that dasatinib is able to block the function of normal human T-lymphocytes in vitro at clinically relevant concentrations. T-cell functions including proliferation, activation and cytokine production were all uniformly inhibited in the presence of dasatinib. We also demonstrated inhibition of TCR signalling through Src-family kinase LCK, and predicted that inhibition of LCK and other kinases involved in T-cell signalling by dasatinib is responsible for the suppression of T-cell function. These findings raise the concern about potential T-cell inhibition in patients taking dasatinib, and suggest a possible application for the treatment of T-cell mediated immune disorders.
- Subjects :
- Antigens, Differentiation, T-Lymphocyte
medicine.drug_class
T-Lymphocytes
Immunology
Dasatinib
Receptors, Antigen, T-Cell
Biology
Lymphocyte Activation
Tyrosine-kinase inhibitor
Interferon-gamma
Antigens, CD
hemic and lymphatic diseases
medicine
Humans
Immunology and Allergy
Lectins, C-Type
Oncogene Proteins v-abl
Protein Kinase Inhibitors
Cell Proliferation
ABL
Kinase
T-cell receptor
Interleukin-2 Receptor alpha Subunit
Imatinib
Protein-Tyrosine Kinases
Thiazoles
Pyrimidines
src-Family Kinases
Cancer research
Tyrosine kinase
Signal Transduction
medicine.drug
Proto-oncogene tyrosine-protein kinase Src
Subjects
Details
- ISSN :
- 15216616
- Volume :
- 127
- Database :
- OpenAIRE
- Journal :
- Clinical Immunology
- Accession number :
- edsair.doi.dedup.....4a7932f4c8db36089335bf8f4da2af55