Evidence map›Paper›PMID 20613786›Full record

ArticleLeukemia2010

Reduced DNAM-1 expression on bone marrow NK cells associated with impaired killing of CD34+ blasts in myelodysplastic syndrome.

M Carlsten, B C Baumann, M Simonsson, M Jädersten, A-M Forsblom, C Hammarstedt, Y T Bryceson, H-G Ljunggren, E Hellström-Lindberg, K-J Malmberg

Registry-linked trialAbstract read
PubMed Publisher
In one paragraph

Article in Leukemia, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05933070 (A Phase I Open-Label Dose Escalation Study Of Intravenous INKmune In Patients With Myelodysplastic Syndrome With Excess Blasts), which is not on this map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
1.3field-weighted citation impact, top 21% 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.

NCT05933070 phase1terminatednot on this mapstarted 2020, after this paper: background citation

A Phase I Open-Label Dose Escalation Study Of Intravenous INKmune In Patients With Myelodysplastic Syndrome With Excess Blasts (MDS-EB-1/2 - MDS-CMML 1/2) Or Acute Myeloid Leukaemia (AML)

TypeinterventionalSponsorInmune Bio, Inc.Ran2020 to 2024Enrolled2ConditionsCancer, MDS-EB, Myelodysplastic Syndromes, Acute Myeloid LeukemiaArmsINKmune
3 · Its place in the literature

Who cites it

67 citing papers in PubMed, 108 citations in OpenAlex.

  1. Review
  2. High frequency of CD95British journal of haematology · 2026
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  19. CD155 and Its Receptors as Targets for Cancer Therapy.International journal of molecular sciences · 2023
    Review
  20. Review

7 more citing papers are in PubMed but not listed here.

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.

M CarlstenDepartment of Medicine, Center for Infectious Medicine, Karolinska Institutet, Karolinska University Hospital Huddinge, Stockholm, Sweden. mattias.carlsten@ki.se
B C Baumann
M Simonsson
M Jädersten
A-M Forsblom
C Hammarstedt
Y T Bryceson
H-G Ljunggren
E Hellström-Lindberg
K-J Malmberg
Karolinska Institutet · SEKarolinska University Hospital · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myelodysplastic syndromes (MDS) comprise a heterogeneous group of clonal stem-cell disorders characterized by ineffective hematopoiesis and risk of progression to acute myeloid leukemia. Increased apoptosis and suppressed functions of peripheral blood natural killer (NK) cells have been described in MDS patients, but only limited information is available on the phenotypic and functional integrity of NK cells in the bone marrow. In a cohort of 41 patients with distinct clinical subtypes of MDS, we here show that NK cells in the bone marrow show decreased surface expression of the activating receptors DNAM-1 and NKG2D. Notably, decreased receptor expression correlated with elevated bone marrow blast counts and was associated with impaired NK-cell responsiveness to stimulation with the K562 cell line, or co-activation by NKG2D or DNAM-1 in combination with the 2B4 receptor. Furthermore, antibody-masking experiments revealed a central role for DNAM-1 in NK cell-mediated killing of freshly isolated MDS blasts. Thus, given the emerging evidence for NK cell-mediated immune surveillance of neoplastic cells, we speculate that reduced expression of DNAM-1 on bone marrow NK cells may facilitate disease progression in patients with MDS.

Indexed as

ApoptosisAdultAgedAged, 80 and overAntigens, CD34Antigens, Differentiation, T-LymphocyteBone Marrow CellsDisease ProgressionFemaleFlow CytometryHumansKiller Cells, NaturalMaleMiddle AgedMyelodysplastic SyndromesT Lineage-Specific Activation Antigen 1Antigens, CD34Antigens, Differentiation, T-LymphocyteT Lineage-Specific Activation Antigen 1

Identifiers

PMID20613786
OpenAlexW2018642917

What OpenQuestion holds

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Registered trials

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.