Evidence map›Paper›PMID 29843224›Full record

ArticleCancer biomarkers : section A of Disease markers2018

Up-regulation of regulatory T cells, CD200 and TIM3 expression in cytogenetically normal acute myeloid leukemia.

Asmaa M Zahran, Mostafa F Mohammed Saleh, Mona M Sayed, Amal Rayan, Arwa Mohammed Ali, Helal F Hetta

Abstract read
In one paragraph

Article in Cancer biomarkers : section A of Disease markers, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

19 citing papers in PubMed, 31 citations in OpenAlex.

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  6. Frontiers in immunology · 2024
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  12. CD200:CD200R Interactions and Their Importance in Immunoregulation.International journal of molecular sciences · 2021
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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

6 authors at 2 institutions in 2 countries.

Asmaa M ZahranClinical Pathology Department, South Egypt Cancer Institute, Assiut University, Assiut, Egypt.
Mostafa F Mohammed SalehClinical Hematology Unit, Internal Medicine Department, Assiut University, Assiut, Egypt.
Mona M SayedRadiation Oncology Department, South Egypt Cancer Institute, Assiut University, Assiut, Egypt.
Amal RayanClinical Oncology Department, Assiut University, Assiut, Egypt.
Arwa Mohammed AliDepartment of Medical Oncology, South Egypt Cancer Institute, Assiut University, Assiut, Egypt.
Helal F HettaDepartment of Medical Microbiology and Immunology, Faculty of Medicine, Assiut University, Assiut, Egypt.
Assiut University · EGORCID · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe bone marrow immunosuppressive microenvironment of AML patients sustains and modulates proliferation, survival and drug resistance of AML through deregulation of both innate and adaptive immune response. We aimed to investigate the level of Tregs, expression of Tim-3 on peripheral blood T cells, expression of CD200 in myeloid blasts in newly diagnosed AML patients with normal cytogenetics (AML-NC) and their prognostic impact. PATIENTS AND

methodsThis study included 40 patients with de novo AML-NC and 20 healthy controls. Flow-cytometry was used for detection of CD4+CD25+high FoxP3+ regulatory T cells, Tim-3 expression on peripheral blood T cells and CD200 expression on myeloid blasts.

resultsThe percentages of CD4+CD25+high and CD4+CD25+high Foxp3+ Tregs were significantly increased in AML patients than controls. The levels of Tregs, Tim-3/CD4+, Tim-3/CD8+, CD200 and MFI of CD200 were significantly lower in responding patients than in those with persistent leukemia. Only high CD200 expression (> 50%) showed statistically significant worse OS with P< 0.04.

conclusionThe increased levels of Tregs, Tim-3 expression on peripheral blood T cells and CD200 expression in myeloid blast in AML patients could play a role in the development of AML. Analysis of these markers could serve as prognostic markers and might guide the therapy in AML patients in the future.

Indexed as

AdultAntigens, CDBiomarkers, TumorBone MarrowBone Marrow CellsCase-Control StudiesCytogenetic AnalysisFemaleFlow CytometryGene ExpressionHepatitis A Virus Cellular Receptor 2HumansImmunophenotypingLeukemia, Myeloid, AcuteLymphocyte CountMaleAntigens, CDantigens, CD200Biomarkers, TumorHAVCR2 protein, humanHepatitis A Virus Cellular Receptor 2acute myeloid leukemiaCD200normal cytogeneticsRegulatory T cellsTIM3

Identifiers

PMID29843224
PMCPMC13078467
OpenAlexW2804688828

What OpenQuestion holds

Textmetadata
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.