Evidence map›Paper›PMID 20483769›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2010

Essential role for TLR9 in prime but not prime-boost plasmid DNA vaccination to activate dendritic cells and protect from lethal viral infection.

Diane Rottembourg, Christophe M Filippi, Damien Bresson, Katrin Ehrhardt, Elizabeth A Estes, Janine E Oldham, Matthias G von Herrath

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

20 citing papers in PubMed, 41 citations in OpenAlex.

  1. International journal of nanomedicine · 2026
    Article
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  3. Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. DNA vaccines: a simple DNA sensing matter?Human vaccines & immunotherapeutics · 2013
    Review
  10. Review
  11. Review
  12. The future of human DNA vaccines.Journal of biotechnology · 2012
    Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Dendritic cell maturation and chemotaxis is regulated by TRPM2-mediated lysosomal Ca2+ release.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2011
    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 1 institution in 1 country.

Diane RottembourgLa Jolla Institute for Allergy and Immunology, La Jolla, CA 92037, USA.
Christophe M Filippi
Damien Bresson
Katrin Ehrhardt
Elizabeth A Estes
Janine E Oldham
Matthias G von Herrath
La Jolla Institute for Immunology · US

Funding

DNA Vaccination &Regulatory Cells in Type I DiabetesR01DK051091 · NIDDK · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI VON HERRATH, MATTHIAS G. · 2003 to 2006
$1.1M
NIDDK NIH HHS R01 DK051091
6 · The paper itself

Abstract

One of the requirements for efficient vaccination against infection is to achieve the best combination of an adequate adjuvant with the antigenic information to deliver. Although plasmid DNA is a promising tool bearing the unique potential to activate humoral and cellular immunity, an actual challenge is to increase plasmid immunogenicity in human vaccination protocols in which efficacy has proven rather limited. Previous work showed that the bacterial DNA backbone of the plasmid has potent adjuvant properties because it contains CpG motifs that are particular activating nucleotidic sequences. Among TLRs, which are key sensors of microbial products, TLR9 can detect CpG motifs and confer activation of APCs, such as dendritic cells. However, whether the immunogenic properties of plasmid DNA involve TLR9 signaling has not been clearly established. In the current study, we demonstrate that TLR9 determines the effectiveness of vaccination against lethal lymphocytic choriomeningitis virus infection using plasmid DNA in a prime, but not prime-boost, vaccination regimen. Furthermore, we provide evidence that the presence of TLR9 in dendritic cells is necessary for effective and functional priming of virus-specific CD8+ T cells upon plasmid exposure in vitro or single-dose vaccination in vivo. Therefore, at single or low vaccine doses that are often used in human-vaccination protocols, CpG/TLR9 interactions participate in the immunogenicity of plasmid DNA. These results suggest that the TLR9 signaling pathway is involved in the efficacy of plasmid vaccination; therefore, it should remain a focus in the development or amelioration of vaccines to treat infections in humans.

Indexed as

AnimalsCD8-Positive T-LymphocytesCell SeparationDendritic CellsFlow CytometryImmunization, SecondaryLymphocyte ActivationLymphocytic ChoriomeningitisLymphocytic choriomeningitis virusMiceMice, Inbred C57BLMice, TransgenicOligodeoxyribonucleotidesPlasmidsSignal TransductionToll-Like Receptor 9CPG-oligonucleotideOligodeoxyribonucleotidesToll-Like Receptor 9Vaccines, DNAViral Vaccines

Identifiers

PMID20483769
PMCPMC3128449
OpenAlexW1918604464

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.