Evidence map›Paper›PMID 8962144›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1996

CGM1a antigen of neutrophils, a receptor of gonococcal opacity proteins.

T Chen, E C Gotschlich

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 92 papers.

0numbers the graph read from it
0cells of the map it votes in
92citing papers in PubMed
8.8field-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

92 citing papers in PubMed, 169 citations in OpenAlex.

  1. C4BP occludes the non-opsonic interaction ofInfection and immunity · 2026
    Article
  2. Article
  3. C4BP occludes the non-opsonic interaction ofbioRxiv : the preprint server for biology · 2026
    Article
  4. Article
  5. Neutrophil CEACAMs and the Inflammatory Response toJournal of innate immunity · 2026
    Review
  6. Review
  7. Experimental Urethral Infection with Neisseria gonorrhoeae.Current topics in microbiology and immunology · 2024
    Review
  8. Article
  9. Discovery of phosphorylated lantibiotics with proimmune activity that regulate the oral microbiome.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Folliculin Controls the Intracellular Survival and Trans-Epithelial Passage ofFrontiers in cellular and infection microbiology · 2020
    Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Frontiers in immunology · 2019
    Article
  20. Journal of oral microbiology · 2019
    Article

32 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

2 authors at 1 institution in 1 country.

T ChenLaboratory of Bacterial Pathogenesis and Immunology, Rockefeller University, New York, NY 10021, USA.
E C Gotschlich
Rockefeller University · US

Funding

IMMUNOCHEMICAL STUDIES ON GONOCOCCAL SURFACE ANTIGENSR01AI010615 · NIAID · ROCKEFELLER UNIVERSITY · PI GOTSCHLICH, EMIL C. · 1985 to 1999
–
NIAID NIH HHS AI 10615
6 · The paper itself

Abstract

Neisseria gonorrhoeae (GC) or Escherichia coli expressing phase-variable opacity (Opa) protein (Opa+ GC or Opa+ E. coli) adhere to human neutrophils and stimulate phagocytosis, whereas their counterparts not expressing Opa protein (Opa- GC or Opa- E. coli) do not. Opa+ GC or E. coli do not adhere to human lymphocytes and promyelocytic cell lines such as HL-60 cells. The adherence of Opa+ GC to the neutrophils can be enhanced dramatically if the neutrophils are preactivated. These data suggest that the components binding the Opa+ bacteria might exist in the granules. CGM1a antigen, a transmembrane protein of the carcinoembryonic antigen family, is exclusively expressed in the granulocytic lineage. The predicted molecular weight of CGM1a is approximately 30 kDa. We observed specific binding of OpaI+ E. coli to a 30-kDa band of polymorphonuclear leukocytes lysates. To prove the hypothesis that the 30-kDa CGM1a antigen from neutrophils was the receptor of Opa+ bacteria, we showed that a HeLa cell line expressing human CGM1a antigen (HeLa-CGM1a) bound Opa+ E. coli and subsequently engulfed the bacteria. Monoclonal antibodies (COL-1) against CGM1 blocked the interaction between Opa+ E. coli and HeLa-CGM1a. These results demonstrate that HeLa cells when expressing the CGM1a antigens bind and internalize OpaI+ bacteria.

Indexed as

Antigens, BacterialBacterial AdhesionBacterial Outer Membrane ProteinsCarcinoembryonic AntigenCell Adhesion MoleculesEscherichia coliHeLa CellsHumansNeutrophilsAntigens, BacterialBacterial Outer Membrane ProteinsCarcinoembryonic AntigenCEACAM3 protein, humanCell Adhesion Moleculesopacity proteins

Identifiers

PMID8962144
PMCPMC26225
OpenAlexW2023160761

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.