Evidence map›Paper›PMID 28474278›Full record

ReviewTargeted oncology2017

Cancer Immunotherapy with Cytokine-Induced Killer Cells.

Juan J Mata-Molanes, Manuel Sureda González, Belén Valenzuela Jiménez, Elena Mª Martínez Navarro, Antonio Brugarolas Masllorens

Abstract readReview
PubMed Publisher
In one paragraph

Review in Targeted oncology, 2017. 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
2.2field-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, 47 citations in OpenAlex.

  1. B cells in cancer: functions, mechanisms and therapeutic advances.Signal transduction and targeted therapy · 2026
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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

5 authors at 1 institution in 1 country.

Juan J Mata-MolanesPlataforma de Oncología, Hospital Quirónsalud Torrevieja, Alicante, Spain. juan.mata@quironsalud.es.
Manuel Sureda GonzálezPlataforma de Oncología, Hospital Quirónsalud Torrevieja, Alicante, Spain.
Belén Valenzuela JiménezPlataforma de Oncología, Hospital Quirónsalud Torrevieja, Alicante, Spain.
Elena Mª Martínez NavarroPlataforma de Oncología, Hospital Quirónsalud Torrevieja, Alicante, Spain.
Antonio Brugarolas MasllorensPlataforma de Oncología, Hospital Quirónsalud Torrevieja, Alicante, Spain.
Hospital Quirón Torrevieja · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cytokine-induced killer (CIK) cells form under certain stimulation conditions in cultures of peripheral blood mononuclear cells (PBMCs). They are a heterogeneous immune cell population and contain a high percentage of cells with a mixed T-NK phenotype (CD3+CD56+). The ready availability of a lymphocyte source, together with the high proliferative rate and potent anti-tumor activity of CIK cells, has allowed their use as immunotherapy in a wide variety of neoplasms. Cytotoxicity mediated by CD3+CD56+ T cells depends on the major histocompatibility antigen (MHC)-independent recognition of tumor cells and the activation of signaling pathways through the natural killer group 2 member D (NKG2D) cell-surface receptor. Clinical trials have demonstrated the feasibility and efficacy of CIK cell immunotherapy even in advanced stage cancer patients or those that have not responded to first-line treatment. This review summarizes biological and technical aspects of CIK cells, as well as past and current clinical trials and future trends in this form of immunotherapy.

Indexed as

AnimalsCancer VaccinesCD3 ComplexCD56 AntigenClinical Trials as TopicCytokine-Induced Killer CellsCytotoxicity, ImmunologicDrug Resistance, NeoplasmHistocompatibility Antigens Class IHumansImmunotherapy, AdoptiveNeoplasmsNeoplasm StagingNK Cell Lectin-Like Receptor Subfamily KSignal TransductionCancer VaccinesCD3 ComplexCD56 AntigenHistocompatibility Antigens Class IKLRK1 protein, humanNK Cell Lectin-Like Receptor Subfamily K

Identifiers

PMID28474278
OpenAlexW2611096344

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.