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Memory T cells skew toward terminal differentiation in the CD8+ T cell population in patients with acute myeloid leukemia
Stem cell memory T (T(SCM)) and central memory T (T(CM)) cells can rapidly differentiate into effector memory (T(EM)) and terminal effector (T(EF)) T cells, and have the most potential for immunotherapy. In this study, we found that the frequency of T(SCM) and T(CM) cells in the CD8+ population dram...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6038290/ https://www.ncbi.nlm.nih.gov/pubmed/29986734 http://dx.doi.org/10.1186/s13045-018-0636-y |
Sumario: | Stem cell memory T (T(SCM)) and central memory T (T(CM)) cells can rapidly differentiate into effector memory (T(EM)) and terminal effector (T(EF)) T cells, and have the most potential for immunotherapy. In this study, we found that the frequency of T(SCM) and T(CM) cells in the CD8+ population dramatically decreased together with increases in T(EM) and T(EF) cells, particularly in younger patients with acute myeloid leukemia (AML) (< 60 years). These alterations persisted in patients who achieved complete remission after chemotherapy. The decrease in T(SCM) and T(CM) together with the increase in differentiated T(EM) and T(EF) subsets in CD8+ T cells may explain the reduced T cell response and subdued anti-leukemia capacity in AML patients. |
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