Evidence map›Paper›PMID 35847700›Full record

ArticleEJHaem2020

PD1 expression on bone marrow T-cells in newly diagnosed Egyptian AML patients: Correlation with hematological parameters, aberrant antigens expression, and response to induction therapy.

Noha Bassiouny, Nour El-Hoda, Ibtesam M Khalifa, Sara Ibrahim, Lamyaa Salem, Layla Annaka

Open access · diamondAbstract read
In one paragraph

Article in EJHaem, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.1field-weighted citation impact, top 59% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. 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

6 authors at 1 institution in 1 country.

Noha BassiounyDepartment of Clinical Pathology Faculty of Medicine Ain Shams University Cairo Egypt.ORCID https://orcid.org/0000-0002-7843-1105
Nour El-HodaDepartment of Internal Medicine and Clinical Hematology Faculty of Medicine Ain Shams University Cairo Egypt.
Ibtesam M KhalifaDepartment of Internal Medicine and Clinical Hematology Faculty of Medicine Ain Shams University Cairo Egypt.
Sara IbrahimDepartment of Clinical Pathology Faculty of Medicine Ain Shams University Cairo Egypt.
Lamyaa SalemDepartment of Clinical Pathology Faculty of Medicine Ain Shams University Cairo Egypt.
Layla AnnakaDepartment of Clinical Pathology Faculty of Medicine Ain Shams University Cairo Egypt.
Ain Shams University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Programed cell death protein 1 (PD-1) is a key mediator for the development of T cell exhaustion that develops in response to persistent antigen stimulation. Aim: In this study, we measured PD1 expression on CD3 positive bone marrow T-lymphocytes in newly diagnosis AML patients and its relation to clinical/ prognostic outcomes in addition to response to induction therapy (day 28). Methods: This study was conducted on 59 newly diagnosed AML patients and 20 healthy controls. Complete blood counts, flow cytometry using acute leukemia panel in addition to PD1 monoclonal antibodies were performed on bone marrow lymphocytes (CD3+), whereas cytogenetic/molecular studies were used to determine risk group. The patients' remission status following induction therapy was determined. Results: PD1 was brightly expressed in 91.5% of the cases than control sample with highly significant difference ( Conclusion: PD1 expression on BM T-cells had a predictive value and providing an immunotherapeutic target for AML.

Indexed as

acute myeloid leukemia (AML)bone marrow (BM)complete remission (CR)flow cytometryprogrammed cell death protein 1 (PD‐1)

Identifiers

PMID35847700
PMCPMC9175862
OpenAlexW3031900733

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.