Evidence map›Paper›PMID 19440334›Full record

ArticlePloS one2009

MGL2 Dermal dendritic cells are sufficient to initiate contact hypersensitivity in vivo.

Yosuke Kumamoto, Kaori Denda-Nagai, Satoshi Aida, Nobuaki Higashi, Tatsuro Irimura

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

32 citing papers in PubMed, 63 citations in OpenAlex.

  1. Article
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  5. Review
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  7. The role of IL-2 in type 2 immunity.Frontiers in immunology · 2025
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  13. A highly polarized TNature immunology · 2020
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  17. CLEC10A Is a Specific Marker for Human CD1cFrontiers in immunology · 2018
    Article
  18. The Origin of Skin Dendritic Cell Network and Its Role in Psoriasis.International journal of molecular sciences · 2017
    Review
  19. Article
  20. CD301beLife · 2016
    Article
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

5 authors at 1 institution in 1 country.

Yosuke KumamotoLaboratory of Cancer Biology and Molecular Immunology, Graduate School of Pharmaceutical Sciences, the University of Tokyo, Tokyo, Japan.
Kaori Denda-Nagai
Satoshi Aida
Nobuaki Higashi
Tatsuro Irimura
The University of Tokyo · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDendritic cells (DCs) are the most potent antigen-presenting cells in the mammalian immune system. In the skin, epidermal Langerhans cells (LCs) and dermal dendritic cells (DDCs) survey for invasive pathogens and present antigens to T cells after migration to the cutaneous lymph nodes (LNs). So far, functional and phenotypic differences between these two DC subsets remain unclear due to lack of markers to identify DDCs. METHODOLOGY/PRINCIPAL

findingsIn the present report, we demonstrated that macrophage galactose-type C-type lectin (MGL) 2 was exclusively expressed in the DDC subset in the skin-to-LN immune system. In the skin, MGL2 was expressed on the majority (about 88%) of MHCII(+)CD11c(+) cells in the dermis. In the cutaneous LN, MGL2 expression was restricted to B220(-)CD8alpha(lo)CD11b(+)CD11c(+)MHCII(hi) tissue-derived DC. MGL2(+)DDC migrated from the dermis into the draining LNs within 24 h after skin sensitization with FITC. Distinct from LCs, MGL2(+)DDCs localized near the high endothelial venules in the outer T cell cortex. In FITC-induced contact hypersensitivity (CHS), adoptive transfer of FITC(+)MGL2(+)DDCs, but not FITC(+)MGL2(-)DCs into naive mice resulted in the induction of FITC-specific ear swelling, indicating that DDCs played a key role in initiation of immune responses in the skin. CONCLUSIONS/SIGNIFICANCE: These results demonstrated the availability of MGL2 as a novel marker for DDCs and suggested the contribution of MGL2(+) DDCs for initiating CHS.

Indexed as

AnimalsAntigens, CDAsialoglycoproteinsCD11b AntigenCD11c AntigenCD8 AntigensCell MovementDermatitis, ContactFlow CytometryLangerhans CellsLectins, C-TypeMembrane ProteinsMiceMice, Inbred BALB CMinor Histocompatibility AntigensReceptors, Cell SurfaceAntigens, CDAsialoglycoproteinsCD11b AntigenCD11c AntigenCD8alpha antigenCD8 AntigensClec10a protein, mouseDEC-205 receptorLectins, C-TypeMembrane ProteinsMGL2 protein, mouseMinor Histocompatibility AntigensReceptors, Cell Surface

Identifiers

PMID19440334
PMCPMC2680031
OpenAlexW2052059484

What OpenQuestion holds

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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.