Evidence map›Paper›PMID 15851484›Full record

ArticleThe Journal of experimental medicine2005

Differential requirements for the chemokine receptor CCR7 in T cell activation during Listeria monocytogenes infection.

Mischo Kursar, Uta E Höpken, Markus Koch, Anne Köhler, Martin Lipp, Stefan H E Kaufmann, Hans-Willi Mittrücker

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The Journal of experimental medicine, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

31 citing papers in PubMed, 65 citations in OpenAlex.

  1. Dysregulated NAMPT signaling underlines the immune-suppressive microenvironment in venous leg ulcers.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
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  3. Splenic stromal niches in homeostasis and immunity.Nature reviews. Immunology · 2023
    Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. CCR7 Deficiency Allows Accelerated Clearance ofJournal of immunology (Baltimore, Md. : 1950) · 2017
    Article
  10. Article
  11. Absence of system xJournal of neuroinflammation · 2017
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. The transcription factor Interferon Regulatory Factor 4 is required for the generation of protective effector CD8+ T cells.Proceedings of the National Academy of Sciences of the United States of America · 2013
    Article
  18. Article
  19. Article
  20. 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

7 authors at 2 institutions in 1 country.

Mischo KursarDepartment of Immunology, Max-Planck Institute for Infection Biology, 10117 Berlin, Germany.
Uta E Höpken
Markus Koch
Anne Köhler
Martin Lipp
Stefan H E Kaufmann
Hans-Willi Mittrücker
Max Planck Institute for Infection Biology · DEMax Delbrück Center · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Effective priming of T cell responses depends on cognate interactions between naive T cells and professional antigen-presenting cells (APCs). This contact is the result of highly coordinated migration processes, in which the chemokine receptor CCR7 and its ligands, CCL19 and CCL21, play a central role. We used the murine Listeria monocytogenes infection model to characterize the role of the CCR7/CCR7 ligand system in the generation of T cell responses during bacterial infection. We demonstrate that efficient priming of naive major histocompatibility complex (MHC) class Ia-restricted CD8+ T cells requires CCR7. In contrast, MHC class Ib-restricted CD8+ T cells and MHC class II-restricted CD4+ T cells seem to be less dependent on CCR7; memory T cell responses are independent of CCR7. Infection experiments with bone marrow chimeras or mice reconstituted with purified T cell populations indicate that CCR7 has to be expressed on CD8+ T cells and professional APCs to promote efficient MHC class Ia-restricted T cell priming. Thus, different T cell subtypes and maturation stages have discrete requirements for CCR7.

Indexed as

AnimalsAntigen-Presenting CellsBone Marrow CellsCD8-Positive T-LymphocytesChemokine CCL19Chemokine CCL21Chemokines, CCDNA PrimersFlow CytometryImmunologic MemoryListeria monocytogenesListeriosisLymphocyte ActivationMajor Histocompatibility ComplexMiceMice, Inbred BALB CCcl19 protein, mouseCcl21c protein, mouseCcr7 protein, mouseChemokine CCL19Chemokine CCL21Chemokines, CCDNA PrimersReceptors, CCR7Receptors, Chemokine

Identifiers

PMID15851484
PMCPMC2213180
OpenAlexW2097296981

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.