Evidence map›Paper›PMID 29628306›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2018

Tumor-Resident Dendritic Cells and Macrophages Modulate the Accumulation of TCR-Engineered T Cells in Melanoma.

Alastair Hotblack, Angelika Holler, Alice Piapi, Sophie Ward, Hans J Stauss, Clare L Bennett

Open access · hybridAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

13 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
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  4. Review
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  8. Article
  9. T Cell Reprogramming Against Cancer.Methods in molecular biology (Clifton, N.J.) · 2020
    Review
  10. Immunotherapy for skin cancer.International immunology · 2019
    Review
  11. Review
  12. Article
  13. Review
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

6 authors at 1 institution in 1 country.

Alastair HotblackInstitute for Immunity and Transplantation, Division of Infection and Immunity, University College London, London NW3 2PF, UK.
Angelika HollerInstitute for Immunity and Transplantation, Division of Infection and Immunity, University College London, London NW3 2PF, UK.
Alice PiapiInstitute for Immunity and Transplantation, Division of Infection and Immunity, University College London, London NW3 2PF, UK.
Sophie WardInstitute for Immunity and Transplantation, Division of Infection and Immunity, University College London, London NW3 2PF, UK; Cancer Institute, Division of Cancer Studies, University College London, London WC1E 6DD, UK.
Hans J StaussInstitute for Immunity and Transplantation, Division of Infection and Immunity, University College London, London NW3 2PF, UK. Electronic address: h.stauss@ucl.ac.uk.
Clare L BennettInstitute for Immunity and Transplantation, Division of Infection and Immunity, University College London, London NW3 2PF, UK; Cancer Institute, Division of Cancer Studies, University College London, London WC1E 6DD, UK. Electronic address: c.bennett@ucl.ac.uk.
University College London · GB

Funding

Medical Research Council MR/K50077X/1
6 · The paper itself

Abstract

Ongoing clinical trials explore T cell receptor (TCR) gene therapy as a treatment option for cancer, but responses in solid tumors are hampered by the immunosuppressive microenvironment. The production of TCR gene-engineered T cells requires full T cell activation in vitro, and it is currently unknown whether in vivo interactions with conventional dendritic cells (cDCs) regulate the accumulation and function of engineered T cells in tumors. Using the B16 melanoma model and the inducible depletion of CD11c

Indexed as

AnimalsAntigens, NeoplasmCD11c AntigenDendritic CellsHeparin-binding EGF-like Growth FactorHumansImmunotherapy, AdoptiveMacrophagesMelanoma, ExperimentalMiceMice, Inbred C57BLMice, KnockoutReceptors, Antigen, T-CellAntigens, NeoplasmCD11c AntigenHeparin-binding EGF-like Growth FactorReceptors, Antigen, T-Celladoptive cellular therapydendritic cellsengineered T cellsmyeloid cellstumor

Identifiers

PMID29628306
PMCPMC5986719
OpenAlexW2792513622

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.