Evidence map›Paper›PMID 36172343›Full record

ReviewFrontiers in immunology2022

Cytokines as an important player in the context of CAR-T cell therapy for cancer: Their role in tumor immunomodulation, manufacture, and clinical implications.

Caio Raony Farina Silveira, Amanda Cristina Corveloni, Sâmia Rigotto Caruso, Nathália Araújo Macêdo, Natália Moscheta Brussolo, Felipe Haddad, Taisa Risque Fernandes, Pamela Viani de Andrade, Maristela Delgado Orellana, Renato Luiz Guerino-Cunha

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed
8.0field-weighted citation impact, top 2% 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

73 citing papers in PubMed, 83 citations in OpenAlex.

  1. Trial
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  4. Review
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  6. Cellular immunotherapy in melanoma: the next frontier in cancer treatment.Journal of experimental & clinical cancer research : CR · 2026
    Review
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  8. Article
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  16. Transient expression of human interleukin-15 inPlant biotechnology (Tokyo, Japan) · 2025
    Article
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  18. Review
  19. Review
  20. Review

13 more citing papers are in PubMed but not listed here.

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

10 authors at 1 institution in 1 country.

Caio Raony Farina SilveiraAdvanced Cellular Therapy Laboratory, Fundação Hemocentro de Ribeirão Preto, São Paulo, Brazil.
Amanda Cristina CorveloniAdvanced Cellular Therapy Laboratory, Fundação Hemocentro de Ribeirão Preto, São Paulo, Brazil.
Sâmia Rigotto CarusoCell Therapy Laboratory, Fundação Hemocentro de Ribeirão Preto, São Paulo, Brazil.
Nathália Araújo MacêdoAdvanced Cellular Therapy Laboratory, Fundação Hemocentro de Ribeirão Preto, São Paulo, Brazil.
Natália Moscheta BrussoloAdvanced Cellular Therapy Laboratory, Fundação Hemocentro de Ribeirão Preto, São Paulo, Brazil.
Felipe HaddadAdvanced Cellular Therapy Laboratory, Fundação Hemocentro de Ribeirão Preto, São Paulo, Brazil.
Taisa Risque FernandesCell Therapy Laboratory, Fundação Hemocentro de Ribeirão Preto, São Paulo, Brazil.
Pamela Viani de AndradeAdvanced Cellular Therapy Laboratory, Fundação Hemocentro de Ribeirão Preto, São Paulo, Brazil.
Maristela Delgado OrellanaCell Therapy Laboratory, Fundação Hemocentro de Ribeirão Preto, São Paulo, Brazil.
Renato Luiz Guerino-CunhaAdvanced Cellular Therapy Laboratory, Fundação Hemocentro de Ribeirão Preto, São Paulo, Brazil.
Fundação Hemopa · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CAR-T cell therapies have been recognized as one of the most advanced and efficient strategies to treat patients with hematologic malignancies. However, similar results have not been observed for the treatment of solid tumors. One of the explanations is the fact that tumors have extremely hostile microenvironments for the infiltration and effector activity of T-cells, mainly due to the presence of highly suppressive cytokines, hypoxia, and reactive oxygen species. Taking advantage of cytokines functionally, new fourth-generation CAR constructs have been developed to target tumor cells and additionally release cytokines that can contribute to the cytotoxicity of T-cells. The manufacturing process, including the use of cytokines in the expansion and differentiation of T cells, is also discussed. Finally, the clinical aspects and the influence of cytokines on the clinical condition of patients, such as cytokine release syndrome, who receive treatment with CAR-T cells are addressed. Therefore, this review aims to highlight how important cytokines are as one of the major players of cell therapy.

Indexed as

NeoplasmsReceptors, Chimeric AntigenCell- and Tissue-Based TherapyCytokinesCytotoxicity, ImmunologicHumansImmunomodulationReactive Oxygen SpeciesTumor MicroenvironmentCytokinesReactive Oxygen SpeciesReceptors, Chimeric Antigencancer microenvironmentCAR-T cellscell therapychimeric antigen receptorcytokinesimmunomodulationimmunotherapy

Identifiers

PMID36172343
PMCPMC9512053
OpenAlexW4295884820

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.