The CD3 versus CD7 plot in multicolor flow cytometry reflects progression of disease stage in patients infected with HTLV-I.
The CD3 versus CD7 plot in multicolor flow cytometry reflects progression of disease stage in patients infected with HTLV-I.
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DOI:
10.1371/journal.pone.0053728
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发表时间:
2013
期刊:
影响因子:
3.7
通讯作者:
Uchimaru K
中科院分区:
文献类型:
--
作者:
Kobayashi S;Tian Y;Ohno N;Yuji K;Ishigaki T;Isobe M;Tsuda M;Oyaizu N;Watanabe E;Watanabe N;Tani K;Tojo A;Uchimaru K
In a recent study to purify adult T-cell leukemia-lymphoma (ATL) cells from acute-type patients by flow cytometry, three subpopulations were observed in a CD3 versus CD7 plot (H: CD3highCD7high; D: CD3dimCD7dim; L: CD3dimCD7low). The majority of leukemia cells were enriched in the L subpopulation and the same clone was included in the D and L subpopulations, suggesting clonal evolution. In this study, we analyzed patients with indolent-type ATL and human T-cell leukemia virus type I (HTLV-I) asymptomatic carriers (ACs) to see whether the CD3 versus CD7 profile reflected progression in the properties of HTLV-I-infected cells. Using peripheral blood mononuclear cells from patient samples, we performed multi-color flow cytometry. Cells that underwent fluorescence-activated cell sorting were subjected to molecular analyses, including inverse long PCR. In the D(%) versus L(%) plot, patient data could largely be categorized into three groups (Group 1: AC; Group 2: smoldering- and chronic-type ATL; and Group 3: acute-type ATL). Some exceptions, however, were noted (e.g., ACs in Group 2). In the follow-up of some patients, clinical disease progression correlated well with the CD3 versus CD7 profile. In clonality analysis, we clearly detected a major clone in the D and L subpopulations in ATL cases and, intriguingly, in some ACs in Group 2. We propose that the CD3 versus CD7 plot reflects progression of disease stage in patients infected with HTLV-I. The CD3 versus CD7 profile will be a new indicator, along with high proviral load, for HTLV-I ACs in forecasting disease progression.
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影响因子:
4.8
作者:
Sasaki, Daisuke;Doi, Yuko;Kamihira, Shimeru
通讯作者:
Kamihira, Shimeru
DOI:
10.1073/pnas.87.17.6713
发表时间:
1990-09-01
影响因子:
11.1
作者:
WILLARDGALLO, KE;VANDEKEERE, F;KETTMANN, R
通讯作者:
KETTMANN, R
影响因子:
20.3
作者:
Iwanaga, Masako;Watanabe, Toshiki;Yamaguchi, Kazunari
通讯作者:
Yamaguchi, Kazunari
影响因子:
45.3
作者:
Tsukasaki, Kunihiro;Hermine, Olivier;Watanabe, Toshiki
通讯作者:
Watanabe, Toshiki
影响因子:
6.5
作者:
YAMAGUCHI, K;KIYOKAWA, T;TAKATSUKI, K
通讯作者:
TAKATSUKI, K