T细胞白血病
生物
淋巴
端粒酶
淋巴结
白血病
抗原
电池类型
细胞
急性白血病
癌症研究
分子生物学
免疫学
病理
医学
基因
遗传学
生物化学
作者
Mariko Mizuguchi,Mitsuyoshi Takatori,Shugo Sakihama,Manami Yoshita‐Takahashi,Naoki Imaizumi,Yoshiaki Takahashi,Hiroo Hasegawa,Kennosuke Karube,Takuya Fukushima,Masataka Nakamura,Yuetsu Tanaka
标识
DOI:10.1038/s41417-022-00475-0
摘要
A massive increase in the number of mature CD4+ T-cells in peripheral blood (PB) is a defining characteristic of acute type of adult T-cell leukemia (ATL). To date, the site of proliferation of ATL cells in the body has been unclear. In an attempt to address this question, we examined the expression of the proliferation marker, Ki-67, in freshly isolated ATL cells from PB and lymph nodes (LNs) of patients with various types of ATL. Our findings reveal that LN-ATL cells display higher expression of the Ki-67 antigen than PB-ATL cells in acute type patients. The gene expression of T-cell quiescence regulators such as Krüppel-like factor 2/6 and forkhead box protein 1 was substantially high in acute type PB-ATL cells. The expression of human telomerase reverse transcriptase, which is involved in T-cell expansion, was significantly low in PB-ATL cells from acute type patients, similar to that in normal resting T-cells. These findings suggest that ATL cells proliferate in the LNs rather than in PB.
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