Evidence map›Paper›PMID 17897047›Full record

ReviewEndocrine, metabolic & immune disorders drug targets2007

Tolerance in the absence of autoantigen.

D W Pascual, J Ochoa-Repáraz, A Rynda, X Yang

Open access · greenAbstract readReview
In one paragraph

Review in Endocrine, metabolic & immune disorders drug targets, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.3field-weighted citation impact, top 41% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Sjögren's Syndrome Treatments in the Microbiome Era.Advances in geriatric medicine and research · 2023
    Article
  3. Article
  4. Regulatory T-cell vaccination independent of auto-antigen.Experimental & molecular medicine · 2014
    Review
  5. Article
  6. Article
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

4 authors at 1 institution in 1 country.

D W PascualVeterinary Molecular Biology, Montana State University, Bozeman, Montana 59717-3610, USA. dpascual@montana.edu
J Ochoa-Repáraz
A Rynda
X Yang
Montana State University · US

Funding

VIRUSES: FROM PARTICLES TO PROTEOMICSP20RR020185 · NCRR · MONTANA STATE UNIVERSITY - BOZEMAN · PI MEISSNER, NICOLE · 2004 to 2011
$17.0M
MUCOSAL IMMUNITY ELICITED BY SALMONELLA VACCINE DELIVERYR01AI041123 · NIAID · MONTANA STATE UNIVERSITY - BOZEMAN · PI PASCUAL, DAVID W · 1999 to 2009
$1.9M
NCRR NIH HHS P20 RR-020185NCRR NIH HHS P20 RR020185NIAID NIH HHS AI-41123NIAID NIH HHS R01 AI041123
6 · The paper itself

Abstract

Regulatory T (T(reg)) cells show promise for treating autoimmune diseases, but their induction to elevated potency has been problematic when the most optimally derived cells are from diseased animals. To circumvent reliance on auto-antigen reactive T(reg) cells, stimulation to vaccine antigens (Ags) may offer a viable alternative while maintaining potency to protect against proinflammatory diseases. Our Salmonella vaccine expressing colonization factor Ag I (CFA/I) possesses anti-inflammatory properties, evident by elevated Th2 cell responses, reduced inflammatory cell infiltrates in the Peyer's patches, and an absence of proinflammatory cytokine production by infected macrophages. Given these findings, we hypothesized whether this vaccine would be protective against experimental autoimmune encephalomyelitis (EAE). As such, Salmonella-CFA/I protected in both prophylactic and therapeutic paradigms against proteolipid protein (PLP(139-151))-mediated EAE in SJL mice. The protected mice showed significantly reduced clinical disease and subsequent resolution when compared to PBS-treated controls. Histopathological studies showed reduced demyelination and no inflammation of spinal cords when compared to PBS- or Salmonella vector-treated mice. To ascertain whether the observed immune deviation was in part supported by T(reg) cells, analysis revealed involvement of FoxP3(+) CD25(+) CD4(+) T cells. Adoptive transfer of induced TGF-beta (+) T(reg) cells from vaccinated mice showed complete protection against PLP(139-151) challenge, but not by naive T(reg) cells. Partial protection to EAE was also achieved by the adoptive transfer of CD25(-) CD4(+) T cells, suggesting that Th2 cells also contributed. Thus, these data show that T(reg) cells are induced by oral vaccination with Salmonella-CFA/I contributing to the efficacious treatment of autoimmune disease.

Indexed as

AnimalsAutoantigensAutoimmune DiseasesEncephalomyelitis, Autoimmune, ExperimentalHumansImmune ToleranceInflammationSalmonella VaccinesT-LymphocytesVaccines, AttenuatedAutoantigensSalmonella VaccinesVaccines, Attenuated

Identifiers

PMID17897047
PMCPMC9811400
OpenAlexW1975911308

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.