Evidence map›Paper›PMID 23792457›Full record

ArticleThe Journal of investigative dermatology2014

CD164 and FCRL3 are highly expressed on CD4+CD26- T cells in Sézary syndrome patients.

Maria Wysocka, Andrew V Kossenkov, Bernice M Benoit, Andrea B Troxel, Elisha Singer, Andras Schaffer, Brian Kim, Tzvete Dentchev, Satoshi Nagata, Tomoko Ise and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of investigative dermatology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

16 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
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  13. Review
  14. TIGIT and Helios Are Highly Expressed on CD4The Journal of investigative dermatology · 2017
    Article
  15. CD164 identifies CD4Archives of dermatological research · 2017
    Article
  16. Article
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

12 authors at 3 institutions in 1 country.

Maria WysockaDepartment of Dermatology, University of Pennsylvania, Philadelphia, Pennsylvania, USA. Electronic address: mwysocka@mail.med.upenn.edu.
Andrew V KossenkovThe Wistar Institute, Philadelphia, Pennsylvania, USA.
Bernice M BenoitDepartment of Dermatology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Andrea B TroxelDepartment of Biostatistics and Epidemiology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Elisha SingerDepartment of Dermatology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Andras SchafferDepartment of Dermatology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Brian KimDepartment of Dermatology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Tzvete DentchevDepartment of Dermatology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Satoshi NagataCancer Biology Research Center, Sanford Research/USD, Sioux Falls, South Dakota, USA.
Tomoko IseCancer Biology Research Center, Sanford Research/USD, Sioux Falls, South Dakota, USA.
Louise C ShoweThe Wistar Institute, Philadelphia, Pennsylvania, USA.
Alain H RookDepartment of Dermatology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
University of Pennsylvania · USSanford Research · USThe Wistar Institute · US

Funding

UNIVERSITY OF PENNSYLVANIA CAN CTR SUPPORT GRANTP30CA016520 · NCI · UNIVERSITY OF PENNSYLVANIA · PI SHELLEY L BERGER · 1985 to 2026
$222.3M
Tumor Microenvironment and MetastasisP30CA010815 · NCI · WISTAR INSTITUTE · PI Dario C Altieri · 1985 to 2026
$75.9M
CENTER FOR CANCER BIOLOGY RESEARCHP20RR024219 · NCRR · SANFORD RESEARCH/USD · PI MISKIMINS, W KEITH · 2011 to 2011
$2.3M
HDAC Inhibitors and CTCLR01CA132098 · NCI · WISTAR INSTITUTE · PI SHOWE, LOUISE C. · 2009 to 2013
$2.0M
Toll Receptor Ligand Therapy of Cutaneous T-Cell LymphomaR01CA122569 · NCI · UNIVERSITY OF PENNSYLVANIA · PI ROOK, ALAIN H · 2008 to 2011
$1.1M
Innate Immune Regulation of Skin InflammationK08AR065577 · NIAMS · WASHINGTON UNIVERSITY · PI KIM, BRIAN · 2014 to 2018
$711k
NCI NIH HHS P30 CA010815NCI NIH HHS P30 CA016520NCI NIH HHS R01 CA122569NCI NIH HHS R01CA122569NCI NIH HHS R01 CA 132098NCI NIH HHS R01 CA132098NCRR NIH HHS 1P20RR024219-01A2NCRR NIH HHS P20 RR024219NIAMS NIH HHS K08 AR065577
6 · The paper itself

Abstract

Sézary syndrome (SS) cells express cell surface molecules also found on normal activated CD4 T cells. In an effort to find a more specific surface marker for malignant SS cells, a microarray analysis of gene expression was performed. Results showed significantly increased levels of mRNA for CD164, a sialomucin found on human CD34+ hematopoietic stem cells, and FCRL3, a molecule present on a subset of human natural T regulatory cells. Both markers were increased in CD4 T cells from SS patients compared with healthy donors (HD). Flow cytometry studies confirmed the increased expression of CD164 and FCRL3 primarily on CD4+CD26- T cells of SS patients. Importantly, a statistically significant correlation was found between an elevated percentage of CD4+CD164+ T cells and an elevated percentage of CD4+CD26- T cells in all tested SS patients but not in patients with mycosis fungoides and atopic dermatitis or HD. FCRL3 expression was significantly increased only in patients with high tumor burden. CD4+CD164+ cells displayed cerebriform morphology and their loss correlated with clinical improvement in treated patients. Our results suggest that CD164 can serve as a marker for diagnosis and for monitoring progression of cutaneous T-cell lymphoma (CTCL)/SS and that FCRL3 expression correlates with a high circulating tumor burden.

Indexed as

BiomarkersCD4-Positive T-LymphocytesCell ShapeDipeptidyl Peptidase 4Disease ProgressionEndolynFlow CytometryHumansMembrane GlycoproteinsMicrofilament ProteinsNeoplastic Cells, CirculatingReceptors, ImmunologicSezary SyndromeTranscriptomeBiomarkersDipeptidyl Peptidase 4DPP4 protein, humanEndolynFCRL3 protein, humanMembrane GlycoproteinsMicrofilament ProteinsplastinReceptors, Immunologic

Identifiers

PMID23792457
PMCPMC3869886
OpenAlexW2052022127

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.