Evidence map›Paper›PMID 19171766›Full record

ArticleThe Journal of experimental medicine2009

Differential rates of replacement of human dermal dendritic cells and macrophages during hematopoietic stem cell transplantation.

Muzlifah Haniffa, Florent Ginhoux, Xiao-Nong Wang, Venetia Bigley, Michal Abel, Ian Dimmick, Sarah Bullock, Marcos Grisotto, Trevor Booth, Peter Taub and 3 more

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The Journal of experimental medicine, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 134 papers.

0numbers the graph read from it
0cells of the map it votes in
134citing papers in PubMed
5.5field-weighted citation impact, top 4% 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

134 citing papers in PubMed, 241 citations in OpenAlex.

  1. Trial
  2. Cutaneous macrophage infiltration in acute GvHD.Bone marrow transplantation · 2015
    Trial
  3. Trial
  4. Trial
  5. Macrophage heterogeneity in human secondary lymphoid organs.Clinical science (London, England : 1979) · 2026
    Review
  6. Establishment of a murine resident dermal macrophage cell line.bioRxiv : the preprint server for biology · 2026
    Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Redefining the human corneal immune compartment using dynamic intravital imaging.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  16. Article
  17. Article
  18. Immune Response in Laser Tattoo Removal: A Systematic Review.Journal of lasers in medical sciences · 2023
    Review
  19. Review
  20. Review

74 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

13 authors at 2 institutions in 2 countries.

Muzlifah HaniffaInstitute of Cellular Medicine, Newcastle University, Newcastle upon Tyne NE2 4HH, England, UK.
Florent Ginhoux
Xiao-Nong Wang
Venetia Bigley
Michal Abel
Ian Dimmick
Sarah Bullock
Marcos Grisotto
Trevor Booth
Peter Taub
Catharien Hilkens
Miriam Merad
Matthew Collin
Newcastle University · GBIcahn School of Medicine at Mount Sinai · US

Funding

Biotechnology and Biological Sciences Research Council BB/E012841/1
6 · The paper itself

Abstract

Animal models of hematopoietic stem cell transplantation have been used to analyze the turnover of bone marrow-derived cells and to demonstrate the critical role of recipient antigen-presenting cells (APC) in graft versus host disease (GVHD). In humans, the phenotype and lineage relationships of myeloid-derived tissue APC remain incompletely understood. It has also been proposed that the risk of acute GVHD, which extends over many months, is related to the protracted survival of certain recipient APC. Human dermis contains three principal subsets of CD45(+)HLA-DR(+) cells: CD1a(+)CD14(-) DC, CD1a(-)CD14(+) DC, and CD1a(-)CD14(+)FXIIIa(+) macrophages. In vitro, each subset has characteristic properties. After transplantation, both CD1a(+) and CD14(+) DC are rapidly depleted and replaced by donor cells, but recipient macrophages can be found in GVHD lesions and may persist for many months. Macrophages isolated from normal dermis secrete proinflammatory cytokines. Although they stimulate little proliferation of naive or memory CD4(+) T cells, macrophages induce cytokine expression in memory CD4(+) T cells and activation and proliferation of CD8(+) T cells. These observations suggest that dermal macrophages and DC are from distinct lineages and that persistent recipient macrophages, although unlikely to initiate alloreactivity, may contribute to GVHD by sustaining the responses of previously activated T cells.

Indexed as

Hematopoietic Stem Cell TransplantationCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell ProliferationCytokinesDendritic CellsFlow CytometryGraft vs Host DiseaseHumansIn Situ Hybridization, FluorescenceMacrophagesMicroscopy, ConfocalCytokines

Identifiers

PMID19171766
PMCPMC2646566
OpenAlexW2164334203

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.