Evidence map›Paper›PMID 19845477›Full record

ArticleAutoimmunity2010

Treatment with a toll-like receptor inhibitory GpG oligonucleotide delays and attenuates lupus nephritis in NZB/W mice.

Kareem L Graham, Lowen Y Lee, John P Higgins, Lawrence Steinman, Paul J Utz, Peggy P Ho

Open access · greenAbstract read
In one paragraph

Article in Autoimmunity, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

17 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
  2. Review
  3. Targeting DAMPs with nucleic acid scavengers to treat lupus.Translational research : the journal of laboratory and clinical medicine · 2022
    Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Toll-like receptors and lupus nephritis.Clinical reviews in allergy & immunology · 2011
    Review
  15. Article
  16. Review
  17. 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

6 authors at 1 institution in 1 country.

Kareem L GrahamDepartment of Medicine, Stanford University School of Medicine, CA 94305, USA.
Lowen Y Lee
John P Higgins
Lawrence Steinman
Paul J Utz
Peggy P Ho
Stanford University · US

Funding

MOLECULAR &CELLULAR IMMUNOBIOLOGYT32AI007290 · NIAID · STANFORD UNIVERSITY · PI Sean Curtis Bendall, Olivia M Martinez · 1985 to 2026
$27.0M
Strategies for Prevention of AutoimmunityU19DK061934 · NIDDK · STANFORD UNIVERSITY · PI FATHMAN, CHARLES GARRISON · 2001 to 2005
$4.4M
Autoantigen Arrays to Select Vaccines for Model of PBCR21AR049328 · NIAMS · STANFORD UNIVERSITY · PI UTZ, PAUL JOSEPH · 2002 to 2003
$159k
THE ROLE OF GRANZYME B IN THE DEVELOPMENT OF MURINE SLEF31AI010663 · NIAID · STANFORD UNIVERSITY · PI GRAHAM, KAREEM L · 2001 to 2003
$130k
NHLBI PROTEOMICS INITIATIVE-N01HV28183N01HV028183 · HV · STANFORD UNIVERSITY · PI NOLAN, GARRY P · 2002 to 2006
–
PLATELET INTERACTIONS WITH FIBRINOGEN AND CALCIUMR01HL028183 · NHLBI · STATE UNIVERSITY NEW YORK STONY BROOK · PI PEERSCHKE, ELLINOR I · 1985 to 1992
–
NHLBI NIH HHS N01 HV028183NHLBI NIH HHS N01-HV-28183NIAID NIH HHS AI10663-02NIAID NIH HHS AI50854NIAID NIH HHS AI50865NIAID NIH HHS F31 AI010663NIAID NIH HHS T32 AI007290NIAMS NIH HHS AR49328NIAMS NIH HHS R21 AR049328NIDDK NIH HHS DK61934NIDDK NIH HHS U19 DK061934
6 · The paper itself

Abstract

Activation of the innate immune system by DNA containing hypomethylated CpG motifs has been implicated in the pathogenesis of systemic lupus erythematosus (SLE). Here, we examined the consequences of immunostimulatory CpG-oligodeoxynucleotide (ODN) and inhibitory GpG-ODN treatment in the NZB x NZW F1 (NZB/W) murine model of SLE. Beginning at 5 months of age, we administered CpG-ODN or GpG-ODN at regular intervals to female NZB/W animals. We also determined the effects of ODN administration on NZB/W mouse lymphocyte function, and the specificity of ODN binding to Toll-like receptors (TLRs) other than TLR-9. While CpG-ODN treatment did not appear to have a major impact on disease severity, GpG-ODN treatment significantly delayed the onset of proteinuria in NZB/W mice. Interestingly, short-term GpG-ODN treatment promoted Th2-type T and B cell responses, and inhibited B lymphocyte proliferation in vitro. On the other hand, extended GpG-ODN treatment did not result in sustained Th2 responses or significantly reduced renal disease. Moreover, the binding of CpG-ODN and GpG-ODN was not restricted to TLR-9 as both ODNs also interacted with TLR-3, TLR-7, and TLR-8. Taken together, the data indicate that the protective mechanism of GpG-ODN treatment in the NZB/W model of lupus nephritis involves modulating T cell cytokine profiles and B lymphocyte activation through the inhibition of several TLRs, including TLR-7 and TLR-9.

Indexed as

AnimalsB-LymphocytesEnzyme-Linked Immunosorbent AssayFemaleLupus NephritisLymphocyte ActivationMiceMice, Inbred C57BLMice, Inbred NZBOligodeoxyribonucleotidesT-LymphocytesT-Lymphocyte SubsetsToll-Like ReceptorsCPG-oligonucleotideGpG-oligonucleotideOligodeoxyribonucleotidesToll-Like Receptors

Identifiers

PMID19845477
PMCPMC4150612
OpenAlexW2076251351

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.