Evidence map›Paper›PMID 28943543›Full record

ArticleInternal medicine (Tokyo, Japan)2017

Expression of Master Regulators of T-cell, Helper T-cell and Follicular Helper T-cell Differentiation in Angioimmunoblastic T-cell Lymphoma.

Yosuke Matsumoto, Hisao Nagoshi, Mihoko Yoshida, Seiichi Kato, Junya Kuroda, Kazuho Shimura, Hiroto Kaneko, Shigeo Horiike, Shigeo Nakamura, Masafumi Taniwaki

Open access · diamondAbstract read
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Article in Internal medicine (Tokyo, Japan), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 35% of its field
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

3 citing papers in PubMed, 7 citations in OpenAlex.

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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

10 authors at 2 institutions in 1 country.

Yosuke MatsumotoDepartments of Hematology and Laboratory Medicine, Aiseikai Yamashina Hospital, Japan.
Hisao NagoshiDivision of Hematology, Kyoto Prefectural University of Medicine, Graduate School of Medical Science, Japan.
Mihoko YoshidaDepartments of Hematology and Laboratory Medicine, Aiseikai Yamashina Hospital, Japan.
Seiichi KatoDepartment of Pathology and Laboratory Medicine, Nagoya University Hospital, Japan.
Junya KurodaDivision of Hematology, Kyoto Prefectural University of Medicine, Graduate School of Medical Science, Japan.
Kazuho ShimuraDepartments of Hematology and Laboratory Medicine, Aiseikai Yamashina Hospital, Japan.
Hiroto KanekoDepartments of Hematology and Laboratory Medicine, Aiseikai Yamashina Hospital, Japan.
Shigeo HoriikeDivision of Hematology, Kyoto Prefectural University of Medicine, Graduate School of Medical Science, Japan.
Shigeo NakamuraDepartment of Pathology and Laboratory Medicine, Nagoya University Hospital, Japan.
Masafumi TaniwakiDepartments of Hematology and Laboratory Medicine, Aiseikai Yamashina Hospital, Japan.
Kyoto Prefectural University of Medicine · JPNagoya University Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective It has been postulated that the normal counterpart of angioimmunoblastic T-cell lymphoma (AITL) is the follicular helper T-cell (TFH). Recent immunological studies have identified several transcription factors responsible for T-cell differentiation. The master regulators associated with T-cell, helper T-cell (Th), and TFH differentiation are reportedly BCL11B, Th-POK, and BCL6, respectively. We explored the postulated normal counterpart of AITL with respect to the expression of the master regulators of T-cell differentiation. Methods We performed an immunohistochemical analysis in 15 AITL patients to determine the expression of the master regulators and several surface markers associated with T-cell differentiation. Results BCL11B was detected in 10 patients (67%), and the surface marker of T-cells (CD3) was detected in all patients. Only 2 patients (13%) expressed the marker of naïve T-cells (CD45RA), but all patients expressed the marker of effector T-cells (CD45RO). Nine patients expressed Th-POK (60%), and 7 (47%) expressed a set of surface antigens of Th (CD4-positive and CD8-negative). In addition, BCL6 and the surface markers of TFH (CXCL13, PD-1, and SAP) were detected in 11 (73%), 8 (53%), 14 (93%), and all patients, respectively. Th-POK-positive/BCL6-negative patients showed a significantly shorter overall survival (OS) than the other patients (median OS: 33.0 months vs. 74.0 months, p=0.020; log-rank test). Conclusion Many of the AITL patients analyzed in this study expressed the master regulators of T-cell differentiation. The clarification of the diagnostic significance and pathophysiology based on the expression of these master regulators in AITL is expected in the future.

Indexed as

AdultAgedAged, 80 and overBiomarkersCell DifferentiationDNA-Binding ProteinsFemaleHumansImmunoblastic LymphadenopathyLymphoma, T-CellMaleMiddle AgedProto-Oncogene Proteins c-bcl-6Repressor ProteinsT-Lymphocytes, Helper-InducerTranscription FactorsBCL11B protein, humanBCL6 protein, humanBiomarkersDNA-Binding ProteinsProto-Oncogene Proteins c-bcl-6Repressor ProteinsTranscription FactorsTumor Suppressor ProteinsZBTB7B protein, humanangioimmunoblastic T-cell lymphomaBCL11BBCL6follicular helper T-cellTh-POK

Identifiers

PMID28943543
PMCPMC5709626
OpenAlexW2759330824

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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.