Evidence map›Paper›PMID 17911600›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2007

Hydrodynamic vaccination with DNA encoding an immunologically privileged retinal antigen protects from autoimmunity through induction of regulatory T cells.

Phyllis B Silver, Rajeev K Agarwal, Shao-Bo Su, Isabelle Suffia, Rafael S Grajewski, Dror Luger, Chi-Chao Chan, Rashid M Mahdi, John M Nickerson, Rachel R Caspi

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

18 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Observational
  6. Tolerance Induction in Relation to the Eye.Frontiers in immunology · 2018
    Review
  7. Immunopathogenic Background of Pars Planitis.Archivum immunologiae et therapiae experimentalis · 2016
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. A look at autoimmunity and inflammation in the eye.The Journal of clinical investigation · 2010
    Review
  14. CD4+Foxp3+ T-regulatory cells in noninfectious uveitis.Archives of ophthalmology (Chicago, Ill. : 1960) · 2009
    Article
  15. Article
  16. Article
  17. Article
  18. 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

10 authors at 2 institutions in 1 country.

Phyllis B SilverLaboratory of Immunology, National Eye Institute, National Institutes of Health Bethesda, MD 20892-1857, USA.
Rajeev K Agarwal
Shao-Bo Su
Isabelle Suffia
Rafael S Grajewski
Dror Luger
Chi-Chao Chan
Rashid M Mahdi
John M Nickerson
Rachel R Caspi
National Institutes of Health · USEmory University · US

Funding

P30-Core Grant for Vision Research Core CP30EY006360 · NEI · EMORY UNIVERSITY · PI NICKERSON, JOHN M · 1986 to 2025
$15.3M
T-CELL LINES AND CLONES IN UVEITAZ01EY000184 · NEI · NATIONAL EYE INSTITUTE · PI CASPI, RACHEL R. · 1985 to 2008
$6.6M
Gene Delivery in Retinal DiseasesR01EY016470 · NEI · EMORY UNIVERSITY · PI NICKERSON, JOHN M · 2006 to 2015
$3.2M
Histology CoreZ01EY000461 · NEI · NATIONAL EYE INSTITUTE · PI CHAN, CHI-CHAO · 2008 to 2008
$416k
Intramural NIH HHS Z01 EY000184NEI NIH HHS P30 EY006360NEI NIH HHS R01 EY016470
6 · The paper itself

Abstract

The eye is an immunologically privileged organ whose Ags serve as targets for experimental autoimmune uveitis (EAU), a model for human uveitis. We used a hydrodynamic i.v. injection of naked DNA to express the uveitogenic retinal Ag interphotoreceptor retinoid-binding protein (IRBP) in the periphery, thus revoking its immune-privileged status. IRBP was expressed in the liver within hours of administration of as little as 10 microg of IRBP-DNA. Vaccinated mice were highly protected from EAU induced by immunization with IRBP for at least 10 wk after vaccination. Protection was partial in a reversal protocol. Mechanistic studies revealed specific hyporesponsiveness to IRBP without immune deviation, no evidence for apoptosis either by the Fas- or Bcl-2-regulated (mitochondrial) pathway and apparent lack of dependence on CD8(+) cells, IL-10, or TGF-beta. In contrast, depletion of CD25(+) cells after vaccination and before challenge markedly abrogated protection. IRBP-specific CD4(+)CD25(high) T cells could be cultured from vaccinated mice and transferred protection to unvaccinated, EAU-challenged recipients. In vitro characterization of these cells revealed that they are Ag specific, anergic, express FoxP3, CTLA-4, and glucocorticoid-induced TNFR, and suppress by contact. Thus, expression of IRBP in the periphery by DNA vaccination results in tolerance that acts at least in part through induction of IRBP-specific, FoxP3(+)CD4(+)CD25(+) regulatory T cells. DNA vaccination may offer a new approach to Ag-specific therapy of uveitis.

Indexed as

Amino Acid SequenceAnimalsAutoimmune DiseasesCell DifferentiationCells, CulturedEye ProteinsHumansInjections, JetLiverLymphocyte ActivationMiceMice, Inbred C3HMice, Inbred C57BLMice, TransgenicMolecular Sequence DataRetinol-Binding ProteinsEye ProteinsRetinol-Binding ProteinsRetinol-Binding Proteins, InterstitialVaccines, DNA

Identifiers

PMID17911600
PMCPMC2761821
OpenAlexW2103732467

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.