Evidence map›Paper›PMID 26289090›Full record

ReviewCancer immunology, immunotherapy : CII2016

Human natural killer cells: news in the therapy of solid tumors and high-risk leukemias.

Gabriella Pietra, Chiara Vitale, Daniela Pende, Alice Bertaina, Francesca Moretta, Michela Falco, Paola Vacca, Elisa Montaldo, Claudia Cantoni, Maria Cristina Mingari and 3 more

Open access · greenAbstract readReview
In one paragraph

Review in Cancer immunology, immunotherapy : CII, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

28 citing papers in PubMed, 35 citations in OpenAlex.

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  15. Exploiting Human NK Cells in Tumor Therapy.Frontiers in immunology · 2019
    Review
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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

13 authors at 6 institutions in 1 country.

Gabriella PietraIRCCS AOU San Martino-IST, Genoa, Italy.
Chiara VitaleIRCCS AOU San Martino-IST, Genoa, Italy.
Daniela PendeIRCCS AOU San Martino-IST, Genoa, Italy.
Alice BertainaIRCCS Ospedale Pediatrico Bambino Gesù, Rome, Italy.
Francesca MorettaDepartment of Medicine, University of Verona, Verona, Italy.
Michela FalcoIstituto Giannina Gaslini, Via G. Gaslini n. 5, 16147, Genoa, Italy.
Paola VaccaDepartment of Experimental Medicine, University of Genova, Genoa, Italy.
Elisa MontaldoIstituto Giannina Gaslini, Via G. Gaslini n. 5, 16147, Genoa, Italy.
Claudia CantoniDepartment of Experimental Medicine, University of Genova, Genoa, Italy.
Maria Cristina MingariIRCCS AOU San Martino-IST, Genoa, Italy.
Alessandro MorettaDepartment of Experimental Medicine, University of Genova, Genoa, Italy.
Franco LocatelliIRCCS Ospedale Pediatrico Bambino Gesù, Rome, Italy.
Lorenzo MorettaIRCCS Ospedale Pediatrico Bambino Gesù, Rome, Italy. lorenzomoretta@opbg.net.
University of Genoa · ITIstituti di Ricovero e Cura a Carattere Scientifico · ITIstituto Giannina Gaslini · ITOspedale Policlinico San Martino · ITBambino Gesù Children's Hospital · ITUniversity of Verona · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It is well established that natural killer (NK) cells play an important role in the immunity against cancer, while the involvement of other recently identified, NK-related innate lymphoid cells is still poorly defined. In the haploidentical hematopoietic stem cell transplantation for the therapy of high-risk leukemias, NK cells have been shown to exert a key role in killing leukemic blasts residual after conditioning. While the clinical results in the cure of leukemias are excellent, the exploitation of NK cells in the therapy of solid tumors is still limited and unsatisfactory. In solid tumors, NK cell function may be inhibited via different mechanisms, occurring primarily at the tumor site. The cellular interactions in the tumor microenvironment involve tumor cells, stromal cells and resident or recruited leukocytes and may favor tumor evasion from the host's defenses. In this context, a number of cytokines, growth factors and enzymes synthesized by tumor cells, stromal cells, suppressive/regulatory myeloid and lymphoid cells may substantially impair the function of different tumor-reactive effector cells, including NK cells. The identification and characterization of such mechanisms may offer clues for the development of new immunotherapeutic strategies to restore effective anti-tumor responses. In order to harness NK cell-based immunotherapies, several approaches have been proposed, including reinforcement of NK cell cytotoxicity by means of specific cytokines, antibodies or drugs. These new tools may improve NK cell function and/or increase tumor susceptibility to NK-mediated killing. Hence, the integration of NK-based immunotherapies with conventional anti-tumor therapies may increase chances of successful cancer treatment.

Indexed as

Cell CommunicationCytotoxicity, ImmunologicHematopoietic Stem Cell TransplantationHumansImmunotherapy, AdoptiveKiller Cells, NaturalLeukemiaModels, ImmunologicalNeoplasmsTumor MicroenvironmentAcute leukemiasHematopoietic stem cell transplantationImmunotherapyInnate lymphoid cellsNK cellsTumor microenvironment

Identifiers

PMID26289090
PMCPMC11028670
OpenAlexW1577253557

What OpenQuestion holds

Textmetadata
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.