Evidence map›Paper›PMID 23555960›Full record

ArticlePloS one2013

A combination of cytokines rescues highly purified leukemic CLL B-cells from spontaneous apoptosis in vitro.

Hussein Ghamlouch, Hakim Ouled-Haddou, Gandhi Damaj, Bruno Royer, Brigitte Gubler, Jean-Pierre Marolleau

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

30 citing papers in PubMed, 41 citations in OpenAlex.

  1. Trial
  2. Polyfunctional CD8Molecular oncology · 2025
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  10. Expanded antigen-experienced CD160Journal for immunotherapy of cancer · 2021
    Article
  11. Article
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  14. Review
  15. Review
  16. A novelOncotarget · 2018
    Article
  17. Review
  18. Article
  19. Review
  20. Cytokine Contents in Chronic Lymphocytic Leukemia: Association with ZAP70 Expression.Turkish journal of haematology : official journal of Turkish Society of Haematology · 2016
    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.

Hussein GhamlouchEA4666, Laboratoire d'Immunologie, Université de Picardie Jules Verne, UFR de Médecine, Amiens, France. hussein.ghamlouch@hotmail.com
Hakim Ouled-Haddou
Gandhi Damaj
Bruno Royer
Brigitte Gubler
Jean-Pierre Marolleau
Université de Picardie Jules Verne · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

B-chronic lymphocytic leukemia (B-CLL), the most common human leukemia, is characterized by predominantly non-dividing malignant mature CD5+ B lymphocytes with an apoptosis defect. Various microenvironmental stimuli confer a growth advantage on these leukemic cells and extend their survival in vivo. Nevertheless, when cultured in vitro, CLL B-cells rapidly die from apoptosis. Certain cytokines may extend the survival capacity of CLL B-cells in vitro and individual anti-apoptotic effects of several cytokines have been reported. The potential cumulative effect of such cytokines has not been studied. We therefore investigated the effects on CLL B-cells survival in vitro of humoral factors, polyclonal lymphocyte activators and a combination of cytokines known for their anti-apoptotic effects. Purified CLL B-cells were cultured in the presence or absence of various soluble molecules and the leukemic cell response was assessed in terms of viability. Apoptotic cell death was detected by flow cytometry using annexinV and 7-amino-actinomycin. The survival of CLL B-cells in vitro was highly variable. When tested separately, cytokines (IL-2, -6, -10, -12, -15, -21, BAFF and APRIL) improved CLL B cell survival moderately; in combination, they significantly enhanced survival of these cells, even up to 7 days of culture. We also report that humoral factors from autologous serum are important for survival of these malignant cells. Our findings support the concept that the CLL microenvironment is critical and suggest that soluble factors may contribute directly to the prolonged survival of CLL B-cells. Therefore, the combination of cytokines we describe as providing strong resistance to apoptosis in vitro might be used to improve the treatment of CLL.

Indexed as

AgedAged, 80 and overApoptosisB-LymphocytesCell SeparationCell SurvivalCytokinesFemaleHumansInterleukin-4Leukemia, Lymphocytic, Chronic, B-CellMaleMiddle AgedTetradecanoylphorbol AcetateTumor Cells, CulturedCytokinesInterleukin-4Tetradecanoylphorbol Acetate

Identifiers

PMID23555960
PMCPMC3608602
OpenAlexW2020029911

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.