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Effects of dasatinib on CD8(+)T, Th1, and Treg cells in patients with chronic myeloid leukemia

OBJECTIVE: To investigate the immunomodulatory effects of the tyrosine kinase inhibitor (TKI) dasatinib on T-cell subtypes in patients with chronic myeloid leukemia (CML). METHODS: T helper (Th) 1, Th2, regulatory T (Treg), and CD8(+)T cell levels were detected in patients with CML (n = 9) before an...

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Detalles Bibliográficos
Autores principales: Wei, Xiaoqing, He, Lin, Wang, Xiaodong, Lin, Min, Dai, Jingying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7607186/
https://www.ncbi.nlm.nih.gov/pubmed/31578901
http://dx.doi.org/10.1177/0300060519877321
Descripción
Sumario:OBJECTIVE: To investigate the immunomodulatory effects of the tyrosine kinase inhibitor (TKI) dasatinib on T-cell subtypes in patients with chronic myeloid leukemia (CML). METHODS: T helper (Th) 1, Th2, regulatory T (Treg), and CD8(+)T cell levels were detected in patients with CML (n = 9) before and after dasatinib treatment. The corresponding response level at the time of a blood test was evaluated. RESULTS: After dasatinib treatment, six patients achieved a better response level, while three did not show improved response levels. Among the total nine patients, there were no significant differences in Th1, Th2, and Treg cell levels, whereas CD8(+)T cell levels were significantly increased after dasatinib treatment compared with before treatment. When we analyzed the six patients who obtained a better response level, Th1 and CD8(+)T cell levels were significantly increased after dasatinib treatment, but Th2 and Treg cell levels did not change. The other three patients who did not have improved response levels showed decreased Th1 cell levels and increased Treg cell levels after treatment. CONCLUSIONS: Dasatinib may increase Th1 and CD8(+)T cell levels, and decrease Treg cell levels in patients with CML. This finding might be associated with a good therapeutic response to this drug.