Evidence map›Paper›PMID 29429633›Full record

ArticleCell2018

NK Cells Stimulate Recruitment of cDC1 into the Tumor Microenvironment Promoting Cancer Immune Control.

Jan P Böttcher, Eduardo Bonavita, Probir Chakravarty, Hanna Blees, Mar Cabeza-Cabrerizo, Stefano Sammicheli, Neil C Rogers, Erik Sahai, Santiago Zelenay, Caetano Reis e Sousa

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in Cell, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06056791 (An Open-label, Phase I/IIa Dose Escalation and Expansion Study to Determine the Safety and Clinical Activity of an Immune Priming Cell Therapy), which is not on this map. Cited by 1,178 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1,178citing papers in PubMed, 1 pooled it
62.9field-weighted citation impact, top 1% 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.

NCT06056791 phase1 / phase2completednot on this mapstarted 2023, after this paper: background citation

An Open-label, Phase I/IIa Dose Escalation and Expansion Study to Determine the Safety and Clinical Activity of an Immune Priming Cell Therapy (INKmune) in Patients With Metastatic Castration Resistant Prostate Cancer (mCRPC)

TypeinterventionalSponsorInmune Bio, Inc.Ran2023 to 2025Enrolled12ConditionsCancer, Metastatic Castration-resistant Prostate Cancer, mCRPCArmsINKmune
3 · Its place in the literature

Who cites it

1,178 citing papers in PubMed, 1 synthesis or guideline pooled it, 1,765 citations in OpenAlex.

  1. Pooled it
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  5. Article
  6. Review
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  12. Cytotoxic CD4Nature aging · 2026
    Article
  13. Article
  14. IL-17D reprograms CD93Cellular & molecular immunology · 2026
    Article
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1,118 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 1 country.

Jan P BöttcherImmunobiology Laboratory, The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK. Electronic address: j.boettcher@tum.de.
Eduardo BonavitaCancer Inflammation and Immunity Group, CRUK Manchester Institute, The University of Manchester, Manchester M20 4BX, UK.
Probir ChakravartyBioinformatics, The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.
Hanna BleesImmunobiology Laboratory, The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.
Mar Cabeza-CabrerizoImmunobiology Laboratory, The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.
Stefano SammicheliImmunobiology Laboratory, The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.
Neil C RogersImmunobiology Laboratory, The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.
Erik SahaiTumour Cell Biology Laboratory, The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.
Santiago ZelenayCancer Inflammation and Immunity Group, CRUK Manchester Institute, The University of Manchester, Manchester M20 4BX, UK.
Caetano Reis e SousaImmunobiology Laboratory, The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK. Electronic address: caetano@crick.ac.uk.
The Francis Crick Institute · GBCancer Research UK Manchester Institute · GBUniversity of Manchester · GB

Funding

Cancer Research UK 15689Cancer Research UK 22255Medical Research CouncilWellcome Trust FC001136
6 · The paper itself

Abstract

Conventional type 1 dendritic cells (cDC1) are critical for antitumor immunity, and their abundance within tumors is associated with immune-mediated rejection and the success of immunotherapy. Here, we show that cDC1 accumulation in mouse tumors often depends on natural killer (NK) cells that produce the cDC1 chemoattractants CCL5 and XCL1. Similarly, in human cancers, intratumoral CCL5, XCL1, and XCL2 transcripts closely correlate with gene signatures of both NK cells and cDC1 and are associated with increased overall patient survival. Notably, tumor production of prostaglandin E2 (PGE

Indexed as

AnimalsCell Line, TumorChemokine CCL5Chemokines, CCyclooxygenase 1Cyclooxygenase 2Dendritic CellsDinoprostoneGene Expression Regulation, NeoplasticHumansKiller Cells, NaturalMelanomaMiceMutationNeoplasmsPrognosisBRAF protein, humanCCL5 protein, humanChemokine CCL5Chemokines, CCyclooxygenase 1Cyclooxygenase 2DinoprostoneProto-Oncogene Proteins B-rafXCL1 protein, humancancer immunotherapydendritic cellsimmune evasiontumor immune controltumor microenvironment

Identifiers

PMID29429633
PMCPMC5847168
OpenAlexW2787835497

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.