Evidence map›Paper›PMID 23349737›Full record

ArticlePloS one2013

The CD3 versus CD7 plot in multicolor flow cytometry reflects progression of disease stage in patients infected with HTLV-I.

Seiichiro Kobayashi, Yamin Tian, Nobuhiro Ohno, Koichiro Yuji, Tomohiro Ishigaki, Masamichi Isobe, Mayuko Tsuda, Naoki Oyaizu, Eri Watanabe, Nobukazu Watanabe and 3 more

Abstract readComparative Study
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Seiichiro KobayashiDivision of Molecular Therapy, Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
Yamin Tian
Nobuhiro Ohno
Koichiro Yuji
Tomohiro Ishigaki
Masamichi Isobe
Mayuko Tsuda
Naoki Oyaizu
Eri Watanabe
Nobukazu Watanabe
Kenzaburo Tani
Arinobu Tojo
Kaoru Uchimaru

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeIn 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: CD3(high)CD7(high); D: CD3(dim)CD7(dim); L: CD3(dim)CD7(low)). 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. EXPERIMENTAL

designUsing 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.

resultsIn 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.

conclusionWe 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.

Indexed as

Disease ProgressionFlow CytometryAdultAgedAntigens, CD7Asymptomatic InfectionsCD3 ComplexColorFemaleHumansHuman T-lymphotropic virus 1Leukemia-Lymphoma, Adult T-CellMaleMiddle AgedPrognosisProtein MultimerizationAntigens, CD7CD3 Complex

Identifiers

PMID23349737
PMCPMC3551918

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.