Evidence map›Paper›PMID 30083264›Full record

ArticleTheranostics2018

Expansion of allogeneic NK cells with efficient antibody-dependent cell cytotoxicity against multiple tumors.

Diego Sanchez-Martinez, Nerea Allende-Vega, Stefania Orecchioni, Giovanna Talarico, Amelie Cornillon, Dang-Nghiem Vo, Celine Rene, Zhao-Yang Lu, Ewelina Krzywinska, Alberto Anel and 8 more

Open access · goldAbstract read
In one paragraph

Article in Theranostics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 13% 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

43 citing papers in PubMed, 1 synthesis or guideline pooled it, 65 citations in OpenAlex.

  1. Pooled it
  2. PolyoxidoniumFrontiers in immunology · 2019
    Trial
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  10. Generation of non-genetically modified, CAR-like, NK cells.Journal for immunotherapy of cancer · 2024
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  12. Article
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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

18 authors at 5 institutions in 2 countries.

Diego Sanchez-MartinezIRMB, Univ Montpellier, INSERM, CHU Montpellier, Montpellier, France.
Nerea Allende-VegaIRMB, Univ Montpellier, INSERM, CHU Montpellier, Montpellier, France.
Stefania OrecchioniLaboratory of Hematology-Oncology, European Institute of Oncology, Milan, Italy.
Giovanna TalaricoLaboratory of Hematology-Oncology, European Institute of Oncology, Milan, Italy.
Amelie CornillonIRMB, Univ Montpellier, INSERM, CHU Montpellier, Montpellier, France.
Dang-Nghiem VoIRMB, Univ Montpellier, INSERM, CHU Montpellier, Montpellier, France.
Celine ReneIRMB, Univ Montpellier, INSERM, CHU Montpellier, Montpellier, France.
Zhao-Yang LuIRMB, Univ Montpellier, INSERM, CHU Montpellier, Montpellier, France.
Ewelina KrzywinskaIRMB, Univ Montpellier, INSERM, CHU Montpellier, Montpellier, France.
Alberto AnelUniversity of Zaragoza/Institute of Health Research of Aragón (IIS-Aragón), Spain.
Eva M GalvezInstituto de Carboquimica, Consejo Superior de Investigaciones Científicas (CSIC).
Julian PardoUniversity of Zaragoza/Institute of Health Research of Aragón (IIS-Aragón), Spain.
Bruno RobertIRCM, INSERM U1194, Univ Montpellier, France.
Pierre MartineauIRCM, INSERM U1194, Univ Montpellier, France.
Yosr HicheriDépartement d'Hématologie Clinique, CHU Montpellier, Univ Montpellier, France.
Francesco BertoliniLaboratory of Hematology-Oncology, European Institute of Oncology, Milan, Italy.
Guillaume CartronDépartement d'Hématologie Clinique, CHU Montpellier, Univ Montpellier, France.
Martin VillalbaIRMB, Univ Montpellier, INSERM, CHU Montpellier, Montpellier, France.
Inserm · FREuropean Institute of Oncology · ITUniversité de Montpellier · FRInstitute for Regenerative Medicine & Biotherapy · FRCentre Hospitalier Universitaire de Montpellier · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Monoclonal antibodies (mAbs) have significantly improved the treatment of certain cancers. However, in general mAbs alone have limited therapeutic activity. One of their main mechanisms of action is to induce antibody-dependent cell-mediated cytotoxicity (ADCC), which is mediated by natural killer (NK) cells. Unfortunately, most cancer patients have severe immune dysfunctions affecting NK activity. This can be circumvented by the injection of allogeneic, expanded NK cells, which is safe. Nevertheless, despite their strong cytolytic potential against different tumors, clinical results have been poor.

Indexed as

Antibody-Dependent Cell CytotoxicityAnimalsAntibodies, MonoclonalAntineoplastic Agents, ImmunologicalDisease Models, AnimalHumansImmunotherapyKiller Cells, NaturalLeukemia, Lymphocytic, Chronic, B-CellMice, SCIDTransplantation, HomologousTreatment OutcomeAntibodies, MonoclonalAntineoplastic Agents, Immunologicalantibody-dependent cell cytotoxicity (ADCC)cancermonoclonal antibodies (mAbs)NK cells

Identifiers

PMID30083264
PMCPMC6071536
OpenAlexW2808995183

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.