Evidence map›Paper›PMID 34361107›Full record

ReviewInternational journal of molecular sciences2021

Dendritic Cells and CCR7 Expression: An Important Factor for Autoimmune Diseases, Chronic Inflammation, and Cancer.

Emma Probst Brandum, Astrid Sissel Jørgensen, Mette Marie Rosenkilde, Gertrud Malene Hjortø

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 82 papers.

0numbers the graph read from it
0cells of the map it votes in
82citing papers in PubMed
8.3field-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.

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

82 citing papers in PubMed, 130 citations in OpenAlex.

  1. Article
  2. Developing Antiviral Vaccines Based on AttenuatedPathogens (Basel, Switzerland) · 2026
    Review
  3. Article
  4. Review
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  6. Article
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  14. Review
  15. Article
  16. Intratumoral delivery of 4-1BBL boosts IL-12-triggered anti-glioma immunity.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  17. Article
  18. Review
  19. Review
  20. Review

22 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

4 authors at 1 institution in 1 country.

Emma Probst BrandumDepartment of Biomedical Sciences, Faculty of Health and Medical Sciences, Blegdamsvej 3B, Room 18.5.32., DK-2200 Copenhagen, Denmark.
Astrid Sissel JørgensenDepartment of Biomedical Sciences, Faculty of Health and Medical Sciences, Blegdamsvej 3B, Room 18.5.32., DK-2200 Copenhagen, Denmark.ORCID 0000-0003-2736-8713
Mette Marie RosenkildeDepartment of Biomedical Sciences, Faculty of Health and Medical Sciences, Blegdamsvej 3B, Room 18.5.32., DK-2200 Copenhagen, Denmark.ORCID 0000-0001-9600-3254
Gertrud Malene HjortøDepartment of Biomedical Sciences, Faculty of Health and Medical Sciences, Blegdamsvej 3B, Room 18.5.32., DK-2200 Copenhagen, Denmark.
University of Copenhagen · DK

Funding

Novo Nordisk Fonden 0057954
6 · The paper itself

Abstract

Chemotactic cytokines-chemokines-control immune cell migration in the process of initiation and resolution of inflammatory conditions as part of the body's defense system. Many chemokines also participate in pathological processes leading up to and exacerbating the inflammatory state characterizing chronic inflammatory diseases. In this review, we discuss the role of dendritic cells (DCs) and the central chemokine receptor CCR7 in the initiation and sustainment of selected chronic inflammatory diseases: multiple sclerosis (MS), rheumatoid arthritis (RA), and psoriasis. We revisit the binary role that CCR7 plays in combatting and progressing cancer, and we discuss how CCR7 and DCs can be harnessed for the treatment of cancer. To provide the necessary background, we review the differential roles of the natural ligands of CCR7, CCL19, and CCL21 and how they direct the mobilization of activated DCs to lymphoid organs and control the formation of associated lymphoid tissues (ALTs). We provide an overview of DC subsets and, briefly, elaborate on the different T-cell effector types generated upon DC-T cell priming. In the conclusion, we promote CCR7 as a possible target of future drugs with an antagonistic effect to reduce inflammation in chronic inflammatory diseases and an agonistic effect for boosting the reactivation of the immune system against cancer in cell-based and/or immune checkpoint inhibitor (ICI)-based anti-cancer therapy.

Indexed as

AnimalsAutoimmune DiseasesDendritic CellsHumansInflammationNeoplasmsReceptors, CCR7Signal TransductionReceptors, CCR7cancerCCR7chronic inflammationdendritic cellMSpsoriasisRA

Identifiers

PMID34361107
PMCPMC8348795
OpenAlexW3191066281

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.