| Literature DB >> 35459881 |
Mariko Mizuguchi1, Mitsuyoshi Takatori2, Shugo Sakihama2, Manami Yoshita-Takahashi3, Naoki Imaizumi4, Yoshiaki Takahashi5, Hiroo Hasegawa6, Kennosuke Karube7,8, Takuya Fukushima8, Masataka Nakamura3, Yuetsu Tanaka9.
Abstract
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.Entities:
Year: 2022 PMID: 35459881 DOI: 10.1038/s41417-022-00475-0
Source DB: PubMed Journal: Cancer Gene Ther ISSN: 0929-1903 Impact factor: 5.987