Evidence map›Paper›PMID 21029863›Full record

ArticleCell2010

Microbial stimulation fully differentiates monocytes to DC-SIGN/CD209(+) dendritic cells for immune T cell areas.

Cheolho Cheong, Ines Matos, Jae-Hoon Choi, Durga Bhavani Dandamudi, Elina Shrestha, M Paula Longhi, Kate L Jeffrey, Robert M Anthony, Courtney Kluger, Godwin Nchinda and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 350 papers.

0numbers the graph read from it
0cells of the map it votes in
350citing papers in PubMed
22.8field-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

350 citing papers in PubMed, 580 citations in OpenAlex.

  1. Article
  2. Specific Biomarkers Involved in Sarcoidosis Diagnosis and Prognosis.International journal of molecular sciences · 2026
    Article
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  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Thymic Dendritic Cells Revisited.Immunological reviews · 2025
    Review
  15. Article
  16. Article
  17. Article
  18. Dendritic cell maturation in cancer.Nature reviews. Cancer · 2025
    Review
  19. Article
  20. Review

290 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 2 institutions in 1 country.

Cheolho CheongChris Browne Center for Immunology and Immune Diseases, The Rockefeller University, New York, NY 10065, USA. ccheong@rockefeller.edu
Ines Matos
Jae-Hoon Choi
Durga Bhavani Dandamudi
Elina Shrestha
M Paula Longhi
Kate L Jeffrey
Robert M Anthony
Courtney Kluger
Godwin Nchinda
Hyein Koh
Anthony Rodriguez
Juliana Idoyaga
Maggi Pack
Klara Velinzon
Chae Gyu Park
Ralph M Steinman
Rockefeller University · USHoward Hughes Medical Institute · US

Funding

Structural Basis of Immune Recognition of Glycosylated AntigensU54GM062116 · NIGMS · SCRIPPS RESEARCH INSTITUTE, THE · PI SASISEKHARAN, RAM · 2001 to 2010
$80.3M
TRANSFORMING TRANSLATIONAL SCIENCE AND EDUCATION TO BENEFIT HUMAN HEALTHUL1RR024143 · NCRR · ROCKEFELLER UNIVERSITY · PI COLLER, BARRY · 2006 to 2011
$49.1M
Dendritic Cells and the Pathogenesis of HIV-1 InfectionR37AI040045 · NIAID · ROCKEFELLER UNIVERSITY · PI STEINMAN, RALPH MARVIN · 2001 to 2010
$6.1M
DENDRITIC CELLS AS ADJUVANTS FOR RESISTANCE TO HIV1R01AI040874 · NIAID · ROCKEFELLER UNIVERSITY · PI STEINMAN, RALPH MARVIN · 1997 to 2008
$4.0M
Identification and vaccine adjuvant responses of dendritic cells in humansR56AI040045 · NIAID · ROCKEFELLER UNIVERSITY · PI SCHLESINGER, SARAH JANE · 2011 to 2011
$520k
DENDRITIC CELLS AND THE PATHOGENESIS OF HIV-1 INFECTIONR01AI040045 · NIAID · ROCKEFELLER UNIVERSITY · PI STEINMAN, RALPH M. · 1996 to 2000
$457k
NCRR NIH HHS UL1 RR024143NCRR NIH HHS UL1RR024143NIAID NIH HHS AI40045NIAID NIH HHS AI40874NIAID NIH HHS N01 AI040045NIAID NIH HHS R01 AI040874NIAID NIH HHS R37 AI040045NIGMS NIH HHS GM62116NIGMS NIH HHS U54 GM062116
6 · The paper itself

Abstract

Dendritic cells (DCs), critical antigen-presenting cells for immune control, normally derive from bone marrow precursors distinct from monocytes. It is not yet established if the large reservoir of monocytes can develop into cells with critical features of DCs in vivo. We now show that fully differentiated monocyte-derived DCs (Mo-DCs) develop in mice and DC-SIGN/CD209a marks the cells. Mo-DCs are recruited from blood monocytes into lymph nodes by lipopolysaccharide and live or dead gram-negative bacteria. Mobilization requires TLR4 and its CD14 coreceptor and Trif. When tested for antigen-presenting function, Mo-DCs are as active as classical DCs, including cross-presentation of proteins and live gram-negative bacteria on MHC I in vivo. Fully differentiated Mo-DCs acquire DC morphology and localize to T cell areas via L-selectin and CCR7. Thus the blood monocyte reservoir becomes the dominant presenting cell in response to select microbes, yielding DC-SIGN(+) cells with critical functions of DCs.

Indexed as

Cell DifferentiationAnimalsAntigen PresentationCell Adhesion MoleculesDC-Specific ICAM-3 Grabbing NonintegrinDendritic CellsEscherichia coliLectins, C-TypeLipopolysaccharide ReceptorsL-SelectinLymph NodesMiceMice, Inbred BALB CMice, Inbred C57BLMonocytesReceptors, CCR7Ccr7 protein, mouseCell Adhesion MoleculesDC-Specific ICAM-3 Grabbing NonintegrinLectins, C-TypeLipopolysaccharide ReceptorsL-SelectinReceptors, CCR7Receptors, Cell SurfaceToll-Like Receptor 4

Identifiers

PMID21029863
PMCPMC3150728
OpenAlexW2083872083

What OpenQuestion holds

Textmetadata
LicenceTDM
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.