Evidence map›Paper›PMID 32117212›Full record

ReviewFrontiers in immunology2019

CEACAM3-A Prim(at)e Invention for Opsonin-Independent Phagocytosis of Bacteria.

Patrizia Bonsignore, Johannes W P Kuiper, Jonas Adrian, Griseldis Goob, Christof R Hauck

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.8field-weighted citation impact, top 17% 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

19 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Neutrophil CEACAMs and the Inflammatory Response toJournal of innate immunity · 2026
    Review
  7. Article
  8. Evolution of CEACAM pathogen decoy receptors in primates.European journal of clinical investigation · 2024
    Article
  9. The role of CEACAMs in neutrophil function.European journal of clinical investigation · 2024
    Review
  10. Article
  11. Article
  12. Article
  13. Mechanisms of host manipulation byFrontiers in microbiology · 2023
    Review
  14. Article
  15. Old and New Blood Markers in Human Colorectal Cancer.International journal of molecular sciences · 2022
    Review
  16. Article
  17. Article
  18. iScience · 2022
    Article
  19. Article
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

5 authors at 1 institution in 1 country.

Patrizia BonsignoreLehrstuhl Zellbiologie, Fachbereich Biologie, Universität Konstanz, Konstanz, Germany.
Johannes W P KuiperLehrstuhl Zellbiologie, Fachbereich Biologie, Universität Konstanz, Konstanz, Germany.
Jonas AdrianLehrstuhl Zellbiologie, Fachbereich Biologie, Universität Konstanz, Konstanz, Germany.
Griseldis GoobLehrstuhl Zellbiologie, Fachbereich Biologie, Universität Konstanz, Konstanz, Germany.
Christof R HauckLehrstuhl Zellbiologie, Fachbereich Biologie, Universität Konstanz, Konstanz, Germany.
University of Konstanz · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Phagocytosis is one of the key innate defense mechanisms executed by specialized cells in multicellular animals. Recent evidence suggests that a particular phagocytic receptor expressed by human polymorphonuclear granulocytes, the carcinoembryonic antigen-related cell adhesion molecule 3 (CEACAM3), is one of the fastest-evolving human proteins. In this focused review, we will try to resolve the conundrum why a conserved process such as phagocytosis is conducted by a rapidly changing receptor. Therefore, we will first summarize the biochemical and structural details of this immunoglobulin-related glycoprotein in the context of the human CEACAM family. The function of CEACAM3 for the efficient, opsonin-independent detection and phagocytosis of highly specialized, host-restricted bacteria will be further elaborated. Taking into account the decisive role of CEACAM3 in the interaction with pathogenic bacteria, we will discuss the evolutionary trajectory of the CEACAM3 gene within the primate lineage and highlight the consequences of CEACAM3 polymorphisms in human populations. From a synopsis of these studies, CEACAM3 emerges as an important component of human innate immunity and a prominent example of a dedicated receptor for professional phagocytosis.

Indexed as

AnimalsBacteriaBiological EvolutionCarcinoembryonic AntigenHumansImmunity, InnatePhagocytosisPrimatesCarcinoembryonic AntigenCEACAM3 protein, humanCEACAM3granulocytehuman innate immunityimmunoreceptor tyrosine-based activation motifITAMpathogenic bacteriaphagocytosissignal transduction

Identifiers

PMID32117212
PMCPMC7026191
OpenAlexW3006280800

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.