Evidence map›Paper›PMID 25699074›Full record

ArticleFrontiers in genetics2015

DNA damage response and evasion from immunosurveillance in CLL: new options for NK cell-based immunotherapies.

Olga M Shatnyeva, Hinrich P Hansen, Katrin S Reiners, Maike Sauer, Maulik Vyas, Elke Pogge von Strandmann

Open access · goldAbstract read
In one paragraph

Article in Frontiers in genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

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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 1 institution in 1 country.

Olga M ShatnyevaInnate Immunity Group, Clinic 1 for Internal Medicine, University of Cologne , Cologne, Germany.
Hinrich P HansenInnate Immunity Group, Clinic 1 for Internal Medicine, University of Cologne , Cologne, Germany.
Katrin S ReinersInnate Immunity Group, Clinic 1 for Internal Medicine, University of Cologne , Cologne, Germany.
Maike SauerInnate Immunity Group, Clinic 1 for Internal Medicine, University of Cologne , Cologne, Germany.
Maulik VyasInnate Immunity Group, Clinic 1 for Internal Medicine, University of Cologne , Cologne, Germany.
Elke Pogge von StrandmannInnate Immunity Group, Clinic 1 for Internal Medicine, University of Cologne , Cologne, Germany.
University of Cologne · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic lymphocytic leukemia (CLL) is the most prominent B cell malignancy among adults in the Western world and characterized by a clonal expansion of B cells. The patients suffer from severe immune defects resulting in increased susceptibility to infections and failure to generate an antitumor immune response. Defects in both, DNA damage response (DDR) pathway and crosstalk with the tissue microenvironment have been reported to play a crucial role for the survival of CLL cells, therapy resistance and impaired immune response. To this end, major advances over the past years have highlighted several T cell immune evasion mechanisms in CLL. Here, we discuss the consequences of an impaired DDR pathway for detection and elimination of CLL cells by natural killer (NK) cells. NK cells are considered to be a major component of the immunosurveillance in leukemia but NK cell activity is impaired in CLL. Restoration of NK cell activity using immunoligands and immunoconstructs in combination with the conventional chemotherapy may provide a future perspective for CLL treatment.

Indexed as

chronic lymphocytic leukemiaDNA damage responseimmunoconstructsimmunoligandsimmunotherapynatural killer cell

Identifiers

PMID25699074
PMCPMC4316781
OpenAlexW2021556109

What OpenQuestion holds

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LicenceCC BY
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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.