Evidence map›Paper›PMID 35355992›Full record

ReviewFrontiers in immunology2022

Control of Dendritic Cell Function Within the Tumour Microenvironment.

Yukti Hari Gupta, Abida Khanom, Sophie E Acton

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 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

48 citing papers in PubMed, 62 citations in OpenAlex.

  1. Trial
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  4. Immunomodulatory Nanozymes as Programmable Redox-Immune Set-Point Regulators.Small (Weinheim an der Bergstrasse, Germany) · 2026
    Review
  5. Marine drugs · 2026
    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

3 authors at 2 institutions in 1 country.

Yukti Hari GuptaStromal Immunology Laboratory, MRC Laboratory for Molecular Cell Biology, University College London, London, United Kingdom.
Abida KhanomStromal Immunology Laboratory, MRC Laboratory for Molecular Cell Biology, University College London, London, United Kingdom.
Sophie E ActonStromal Immunology Laboratory, MRC Laboratory for Molecular Cell Biology, University College London, London, United Kingdom.
MRC Laboratory for Molecular Cell Biology · GBUniversity College London · GB

Funding

Cancer Research UK 19763
6 · The paper itself

Abstract

The tumour microenvironment (TME) presents a major block to anti-tumour immune responses and to effective cancer immunotherapy. The inflammatory mediators such as cytokines, chemokines, growth factors and prostaglandins generated in the TME alter the phenotype and function of dendritic cells (DCs) that are critical for a successful adaptive immune response against the growing tumour. In this mini review we discuss how tumour cells and the surrounding stroma modulate DC maturation and trafficking to impact T cell function. Fibroblastic stroma and the associated extracellular matrix around tumours can also provide physical restrictions to infiltrating DCs and other leukocytes. We discuss interactions between the inflammatory TME and infiltrating immune cell function, exploring how the inflammatory TME affects generation of T cell-driven anti-tumour immunity. We discuss the open question of the relative importance of antigen-presentation site; locally within the TME versus tumour-draining lymph nodes. Addressing these questions will potentially increase immune surveillance and enhance anti-tumour immunity.

Indexed as

NeoplasmsTumor MicroenvironmentAntigen PresentationDendritic CellsHumansT-Lymphocytesanti-tumour immunitydendritic cellsdraining lymph nodesimmune infiltrationinflammatory cytokinesTertiary Lymphoid Structures (TLS)tumour microenvironment (TME)

Identifiers

PMID35355992
PMCPMC8960065
OpenAlexW4220753874

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.