Evidence map›Paper›PMID 10903336›Full record

ArticleThe Journal of clinical investigation2000

Treatment of murine lupus with cDNA encoding IFN-gammaR/Fc.

B R Lawson, G J Prud'homme, Y Chang, H A Gardner, J Kuan, D H Kono, A N Theofilopoulos

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
14.4field-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

50 citing papers in PubMed, 158 citations in OpenAlex.

  1. Article
  2. IFN-γ, should not be ignored in SLE.Frontiers in immunology · 2022
    Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. TLRs and IFNs: critical pieces of the autoimmunity puzzle.The Journal of clinical investigation · 2012
    Review
  14. Biological therapy in systemic lupus erythematosus.International journal of rheumatology · 2012
    Article
  15. Review
  16. Interferons in autoimmune and inflammatory diseases: regulation and roles.Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research · 2011
    Review
  17. Novel treatments for systemic lupus erythematosus.Therapeutic advances in musculoskeletal disease · 2011
    Article
  18. Review
  19. Murine models of systemic lupus erythematosus.Journal of biomedicine & biotechnology · 2011
    Review
  20. Th subset balance in lupus nephritis.Journal of biomedicine & biotechnology · 2011
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 2 countries.

B R LawsonDepartment of Immunology, The Scripps Research Institute, La Jolla, California, USA.
G J Prud'homme
Y Chang
H A Gardner
J Kuan
D H Kono
A N Theofilopoulos
Scripps Research Institute · USMcGill University · CA

Funding

T Cell Homeostasis in Systemic AutoimmunityR01AR031203 · NIAMS · SCRIPPS RESEARCH INSTITUTE, THE · PI THEOFILOPOULOS, ARGYRIOS N · 1986 to 2012
$4.9M
Genetic Basis of Systemic AutoimmunityR37AR039555 · NIAMS · SCRIPPS RESEARCH INSTITUTE, THE · PI THEOFILOPOULOS, ARGYRIOS N · 2003 to 2012
$4.2M
T CELL ANTIGEN RECEPTOR GENES IN AUTOIMMUNITYR01AR039555 · NIAMS · SCRIPPS RESEARCH INSTITUTE · PI THEOFILOPOULOS, ARGYRIOS N · 1988 to 2002
$1.4M
CELL CYCLE AND APOPTOSIS GENES IN IMMUNOLOGIC SENESCENCER01AG015061 · NIA · SCRIPPS RESEARCH INSTITUTE · PI THEOFILOPOULOS, ARGYRIOS N · 1998 to 2002
$907k
NEUROBIOLOGIC AND IMMUNOLOGIC ASPECTS OF AGINGT32AG000080 · NIA · SCRIPPS RESEARCH INSTITUTE · PI BUXBAUM, JOEL N · 1985 to 2003
$743k
NIAMS NIH HHS AR31203NIAMS NIH HHS AR39555NIAMS NIH HHS R01 AR031203NIAMS NIH HHS R01 AR039555NIAMS NIH HHS R37 AR039555NIA NIH HHS AG15061NIA NIH HHS T32 AG000080
6 · The paper itself

Abstract

IFN-gamma, a pleiotropic cytokine, is a key effector molecule in the pathogenesis of several autoimmune diseases, including lupus. Importantly, deletion of IFN-gamma or IFN-gammaR in several lupus-predisposed mouse strains resulted in significant disease reduction, suggesting the potential for therapeutic intervention. We evaluated whether intramuscular injections of plasmids with cDNA encoding IFN-gammaR/Fc can retard lupus development and progression in MRL-Fas(lpr) mice. Therapy significantly reduced serum levels of IFN-gamma, as well as disease manifestations (autoantibodies, lymphoid hyperplasia, glomerulonephritis, mortality), when treatment was initiated at the predisease stage, particularly when IFN-gammaR/Fc expression was enhanced by electroporation at the injection site. Remarkably, disease was arrested and even ameliorated when this treatment was initiated at an advanced stage. This therapy represents a rare example of disease reversal and makes application of this nonviral gene therapy in humans with lupus (and perhaps other autoimmune/inflammatory conditions) highly promising.

Indexed as

AnimalsChromatinDNA, ComplementaryGenetic Predisposition to DiseaseGenetic TherapyHyperplasiaImmunoglobulin Fc FragmentsImmunoglobulin GInjections, IntramuscularInterferon-gammaInterferon gamma ReceptorKidneyLupus Erythematosus, SystemicLymphoid TissueMiceMice, Inbred MRL lprChromatinDNA, ComplementaryImmunoglobulin Fc FragmentsImmunoglobulin GInterferon-gammaInterferon gamma ReceptorReceptors, InterferonRecombinant Fusion Proteins

Identifiers

PMID10903336
PMCPMC314313
OpenAlexW2156451662

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.