Evidence map›Paper›PMID 8823297›Full record

ArticleThe Journal of clinical investigation1996

Oral insulin treatment suppresses virus-induced antigen-specific destruction of beta cells and prevents autoimmune diabetes in transgenic mice.

M G von Herrath, T Dyrberg, M B Oldstone

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
9.0field-weighted citation impact, top 2% 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

35 citing papers in PubMed, 152 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Non-antigenic and antigenic interventions in type 1 diabetes.Human vaccines & immunotherapeutics · 2014
    Review
  5. Emerging Trends in Noninvasive Insulin Delivery.Journal of pharmaceutics · 2014
    Review
  6. Trials in type 1 diabetes: Antigen-specific therapies.Clinical immunology (Orlando, Fla.) · 2013
    Review
  7. Inducing immune tolerance: a focus on Type 1 diabetes mellitus.Diabetes management (London, England) · 2013
    Article
  8. Article
  9. Article
  10. Review
  11. 2011 Update: antigen-specific therapy in type 1 diabetes.Current opinion in endocrinology, diabetes, and obesity · 2011
    Review
  12. Article
  13. Article
  14. Review
  15. Review
  16. AAV8-mediated gene transfer of interleukin-4 to endogenous beta-cells prevents the onset of diabetes in NOD mice.Molecular therapy : the journal of the American Society of Gene Therapy · 2008
    Article
  17. Review
  18. Review
  19. Article
  20. 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

3 authors at 2 institutions in 2 countries.

M G von HerrathDepartment of Neuropharmacology, Scripps Research Institute, La Jolla, California 92037, USA. matthias@scripps.edu
T Dyrberg
M B Oldstone
Scripps Research Institute · USNovo Nordisk (Denmark) · DK

Funding

VIROLOGY AND IMMUNOLOGY OF AGINGP01AG004342 · NIA · SCRIPPS RESEARCH INSTITUTE, THE · PI WILLIAMSON, R ANTHONY · 1985 to 2008
$12.9M
NIA NIH HHS AG00080NIA NIH HHS AG04342NIDDK NIH HHS DK49836
6 · The paper itself

Abstract

Oral administration of self-antigens has been proposed as a therapy to prevent and treat autoimmune diseases. Here we report that oral treatment with insulin prevents virus-induced insulin-dependent diabetes mellitus (IDDM) in a transgenic (tg) mouse model. Such mice express the viral nucleoprotein (NP) of lymphocytic choriomeningitis virus (LCMV) under control of the rat insulin promoter in their pancreatic beta cells and < 2% spontaneously develop diabetes. However, 2 mo after challenge with LCMV, IDDM occurs in > 95% of tg mice but not in controls. Oral treatment with 1 mg of insulin twice per week for 2 mo starting either 1 wk before or 10 d after initiating LCMV infection prevents IDDM in > 50% of the tg mice (observation time 8 mo). Thus, insulin therapy is effective in preventing progression to overt IDDM in prediabetic tg mice with ongoing islet infiltration. Oral administration of insulin does not affect the generation of LCMV-NP-specific anti-self cytotoxic T lymphocytes nor the infiltration of lymphocytes into the pancreas. However, less beta cells are destroyed in insulin-treated mice, upregulation of MHC class I and II molecules does not occur, and antiviral (self) cytotoxic T lymphocytes are not found in the islets, events present in tg mice developing IDDM. The majority of lymphocytes in the islets of insulin-treated tg mice without IDDM produces IL-4, IL-10, and TGF-beta. In contrast, lymphocytes from islets of tg mice developing IDDM mainly make gamma-IFN.

Indexed as

Administration, OralAnimalsAutoimmunityB-LymphocytesCell MovementDiabetes Mellitus, ExperimentalHistocompatibility Antigens Class IHistocompatibility Antigens Class IIHypoglycemic AgentsImmunohistochemistryInsulinInterferon-gammaInterleukin-10Interleukin-4Islets of LangerhansLymphocytic choriomeningitis virusHistocompatibility Antigens Class IHistocompatibility Antigens Class IIHypoglycemic AgentsInsulinInterferon-gammaInterleukin-10Interleukin-4NucleoproteinsTransforming Growth Factor beta

Identifiers

PMID8823297
PMCPMC507558
OpenAlexW2161817457

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.