Evidence map›Paper›PMID 9050886›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1997

Peptide inhibition of glomerular deposition of an anti-DNA antibody.

B Gaynor, C Putterman, P Valadon, L Spatz, M D Scharff, B Diamond

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed
6.8field-weighted citation impact, top 3% 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

71 citing papers in PubMed, 189 citations in OpenAlex.

  1. Review
  2. Article
  3. Peptide-based immunotherapy in lupus: Where are we now?Rheumatology and immunology research · 2023
    Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Review
  18. DNA-reactive B cells in lupus.Current opinion in immunology · 2016
    Review
  19. Article
  20. Article

11 more citing papers are in PubMed but not listed here.

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 3 institutions in 2 countries.

B GaynorDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
C Putterman
P Valadon
L Spatz
M D Scharff
B Diamond
Albert Einstein College of Medicine · USYeshiva University · USBipar · FR

Funding

ANTIDNA ANTIBODIES IN SYSTEMIC LUPUS ERYTHEMATOSUSR37AR032371 · NIAMS · YESHIVA UNIVERSITY · PI DIAMOND, BETTY · 1996 to 2005
$3.0M
SELF PEPTIDE DISPLAY BY MHC MOLECULESP01AI033184 · NIAID · YESHIVA UNIVERSITY · PI DIAMOND, BETTY · 1992 to 1996
–
ANTIDNA ANTIBODIES IN SYSTEMIC LUPUS ERYTHEMATOSUSR01AR032371 · NIAMS · YESHIVA UNIVERSITY · PI DIAMOND, BETTY · 1986 to 1995
–
NIAID NIH HHS AI33184NIAID NIH HHS P01 AI33184NIAMS NIH HHS AR32371NIAMS NIH HHS R37 AR032371
6 · The paper itself

Abstract

Antibodies to double-stranded DNA are pathognomonic of systemic lupus erythematosus and deposit in the kidneys of lupus patients to cause glomerulonephritis. Recent data suggest that a significant proportion of anti-DNA antibodies may cross-react with renal antigens and be sequestered in the kidney by virtue of this cross-reactivity. If this is true, antigenic competition for pathogenic antibodies might prevent their deposition in kidneys and the ensuing tissue damage. To generate surrogate antigens that could be used for this purpose, we have used peptide display phage libraries to identify peptides that react with R4A, a pathogenic mouse monoclonal anti-DNA antibody that deposits in glomeruli. We have demonstrated that the peptides bind in or near the double-stranded DNA binding site. Furthermore, the peptides are bound preferentially by the R4A antibody as compared with two closely related antibodies derived from it, one of which deposits in renal tubules and one of which displays no renal pathogenicity. Administration of one of these peptides in a soluble form protects mice from renal deposition of the R4A anti-DNA antibody in vivo. This represents a new therapeutic approach in systemic lupus erythematosus that focuses on protecting target organs from antibody mediated injury.

Indexed as

AnimalsAntibodies, AntinuclearAntibodies, MonoclonalBacteriophagesBinding Sites, AntibodyDNAEnzyme-Linked Immunosorbent AssayImmunohistochemistryKidney GlomerulusLupus Erythematosus, SystemicMiceMice, SCIDPeptide LibraryPeptidesPrecipitin TestsProtein BindingAntibodies, AntinuclearAntibodies, MonoclonalDNAPeptide LibraryPeptides

Identifiers

PMID9050886
PMCPMC20024
OpenAlexW2010957725

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.