Evidence map›Paper›PMID 11717440›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2001

Structural basis for autoantibody recognition of phosphatidylserine-beta 2 glycoprotein I and apoptotic cells.

B A Cocca, S N Seal, P D'Agnillo, Y M Mueller, P D Katsikis, J Rauch, M Weigert, M Z Radic

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

31 citing papers in PubMed, 103 citations in OpenAlex.

  1. Article
  2. Article
  3. Anti-βClinical and experimental immunology · 2019
    Article
  4. Review
  5. B-CD8Journal of immunology research · 2017
    Article
  6. Article
  7. The analysis of clonal expansions in normal and autoimmune B cell repertoires.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2015
    Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Antibodies that bind complex glycosaminoglycans accumulate in the Golgi.Proceedings of the National Academy of Sciences of the United States of America · 2013
    Article
  14. Article
  15. Protective Roles of Natural IgM Antibodies.Frontiers in immunology · 2012
    Article
  16. Article
  17. The consequences of apoptosis in autoimmunity.Journal of autoimmunity · 2008
    Review
  18. Article
  19. Editing and escape from editing in anti-DNA B cells.Proceedings of the National Academy of Sciences of the United States of America · 2008
    Article
  20. Lupus nephritis: the central role of nucleosomes revealed.The American journal of pathology · 2008
    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

8 authors at 3 institutions in 2 countries.

B A CoccaDepartment of Microbiology and Immunology, MCP Hahnemann University, Philadelphia, PA 19129, USA.
S N Seal
P D'Agnillo
Y M Mueller
P D Katsikis
J Rauch
M Weigert
M Z Radic
McGill University · CAMontreal General Hospital · CAPrinceton University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Apoptotic cells contain nuclear autoantigens that may initiate a systemic autoimmune response. To explore the mechanism of antibody binding to apoptotic cells, 3H9, a murine autoantibody with dual specificity for phospholipids and DNA, was used. H chain mutants of 3H9 were constructed, expressed as single-chain Fv (scFv) in Escherichia coli, and assessed for binding to phosphatidylserine, an antigen expressed on apoptotic cells. Both 3H9 and its germline revertant bound to dioleoyl phosphatidylserine in ELISA, and binding was enhanced by beta 2 glycoprotein I (beta 2GPI), a plasma protein that selectively binds to apoptotic cells. Higher relative affinity for DOPS-beta 2GPI was achieved by the introduction of Arg residues into the 3H9 H chain variable region at positions previously shown to mediate DNA binding. Specificity of the two structurally most diverse scFv for apoptotic cells was shown by flow cytometry, and two populations of scFv-bound cells were identified by differences in propidium iodide staining. The results suggest that, in autoimmunity, B cells with Ig receptors for apoptotic cells and DNA are positively selected, and that the antibodies they produce have the potential to affect the clearance and processing of apoptotic cells.

Indexed as

Amino Acid SequenceAntibodies, AntinuclearAntibodies, AntiphospholipidApoptosisbeta 2-Glycoprotein IDNAGlycoproteinsHumansImmunoglobulin FragmentsImmunoglobulin Heavy ChainsImmunoglobulin Variable RegionJurkat CellsModels, MolecularMolecular Sequence DataMutagenesis, Site-DirectedPhosphatidylserines1,2-dioleoylphosphatidylserine3H9 protein, mouseAntibodies, AntinuclearAntibodies, Antiphospholipidbeta 2-Glycoprotein IDNAGlycoproteinsImmunoglobulin Fragmentsimmunoglobulin FvImmunoglobulin Heavy ChainsImmunoglobulin Variable RegionPhosphatidylserines

Identifiers

PMID11717440
PMCPMC61126
OpenAlexW2019650966

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.