Evidence map›Paper›PMID 10430938›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1999

CpG DNA: a potent signal for growth, activation, and maturation of human dendritic cells.

G Hartmann, G J Weiner, A M Krieg

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 116 papers.

0numbers the graph read from it
0cells of the map it votes in
116citing papers in PubMed
20.0field-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

116 citing papers in PubMed, 624 citations in OpenAlex.

  1. Article
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  10. Article
  11. Review
  12. CpG-Based Nanovaccines for Cancer Immunotherapy.International journal of nanomedicine · 2021
    Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Quantification of CpG Motifs in rAAV Genomes: Avoiding the Toll.Molecular therapy : the journal of the American Society of Gene Therapy · 2020
    Review
  18. Codon Modification and PAMPs in Clinical AAV Vectors: The Tortoise or the Hare?Molecular therapy : the journal of the American Society of Gene Therapy · 2020
    Article
  19. Article
  20. Review

56 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

3 authors at 1 institution in 1 country.

G HartmannDepartment of Internal Medicine and the University of Iowa Cancer Center, University of Iowa, Iowa City, IA 52242, USA.
G J Weiner
A M Krieg
PhytoCeutica (United States) · US

Funding

SITE SPECIFIC ANTIINSULIN RECEPTOR ANTIBODIESP30DK025295 · NIDDK · UNIVERSITY OF IOWA · PI BAR, ROBERT S · 1986 to 2002
$2.6M
ROLE OF CD45 IN LYMPHOCYTE ACTIVATIONP01CA066570 · NCI · UNIVERSITY OF PENNSYLVANIA · PI KORETZKY, GARY A. · 1996 to 2000
$775k
NCI NIH HHS P01CA66570NIDDK NIH HHS DK25295
6 · The paper itself

Abstract

DNA molecules containing unmethylated CpG-dinucleotides in particular base contexts ("CpG motifs") are excellent adjuvants in rodents, but their effects on human cells have been less clear. Dendritic cells (DCs) form the link between the innate and the acquired immune system and may influence the balance between T helper 1 (Th1) and Th2 immune responses. We evaluated the effects of CpG oligodeoxynucleotides alone or in combination with granulocyte-macrophage colony-stimulating factor (GMCSF) on different classes of purified human DCs. For primary dendritic precursor cells isolated from human blood, CpG oligonucleotides alone were superior to GMCSF in promoting survival and maturation (CD83 expression) as well as expression of class II MHC and the costimulatory molecules CD40, CD54, and CD86 of DCs. Both CD4-positive and CD4-negative peripheral blood dendritic precursor cells responded to CpG DNA which synergized with GMCSF but these DCs showed little response to lipopolysaccharide (LPS). In contrast, monocyte-derived DCs did not respond to CpG, but they were highly sensitive to LPS, suggesting an inverse correlation between CpG and LPS sensitivity in different subsets of DCs. Compared with GMCSF, CpG-treated peripheral blood DCs showed enhanced functional activity in the mixed lymphocyte reaction and induced T cells to secrete increased levels of Th1 cytokines. These findings demonstrate the ability of specific CpG motifs to strongly activate certain subsets of human DCs to promote Th1-like immune responses, and support the use of CpG DNA-based trials for immunotherapy against cancer, allergy, and infectious diseases.

Indexed as

Adjuvants, ImmunologicAnimalsAntigens, CDBase SequenceB-LymphocytesCells, CulturedDendritic CellsDinucleoside PhosphatesDNADNA MethylationFlow CytometryGene Expression RegulationGenes, MHC Class IIHLA-D AntigensHumansIntercellular Adhesion Molecule-1Adjuvants, ImmunologicAntigens, CDCpG dinucleotideDinucleoside PhosphatesDNAHLA-D AntigensIntercellular Adhesion Molecule-1LipopolysaccharidesOligodeoxyribonucleotides

Identifiers

PMID10430938
PMCPMC17777
OpenAlexW2037233457

What OpenQuestion holds

Textmetadata
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.