Evidence map›Paper›PMID 22288608›Full record

ReviewAnnals of the New York Academy of Sciences2012

Siglecs as sensors of self in innate and adaptive immune responses.

James C Paulson, Matthew S Macauley, Norihito Kawasaki

Abstract readReview
In one paragraph

Review in Annals of the New York Academy of Sciences, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

60 citing papers in PubMed, 115 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. A dual role for PGLYRP1 in host defense and immune regulation duringbioRxiv : the preprint server for biology · 2025
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Tumor suppressionChemical science · 2022
    Article
  15. Article
  16. Review
  17. Regulation of prognosis-related Siglecs in the glioma microenvironment.Journal of cancer research and clinical oncology · 2021
    Article
  18. Extracellular matrix protein N-glycosylation mediates immune self-tolerance inProceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  19. Siglecs-7/9 function as inhibitory immune checkpoints in vivo and can be targeted to enhance therapeutic antitumor immunity.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  20. 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

3 authors at 1 institution in 1 country.

James C PaulsonDepartment of Chemical Physiology, The Scripps Research Institute, La Jolla, California 92037, USA. jpaulson@scripps.edu
Matthew S Macauley
Norihito Kawasaki
Scripps Research Institute · US

Funding

REGULATION OF SIALOSIDE EXPRESSION IN LEUKOCYTESR01AI050143 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI PAULSON, JAMES C · 2003 to 2018
$7.0M
Inducing antigen specific B cell toleranceR01AI099141 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI PAULSON, JAMES C · 2012 to 2016
$2.3M
In vivo targeting of hematopoetic cells with glycan ligands of siglecsR01CA138891 · NCI · SCRIPPS RESEARCH INSTITUTE, THE · PI PAULSON, JAMES C · 2010 to 2014
$1.9M
NCI NIH HHS CA138891NCI NIH HHS R01 CA138891NIAID NIH HHS AI050143NIAID NIH HHS R01 AI050143NIAID NIH HHS R01 AI099141
6 · The paper itself

Abstract

Siglecs are expressed on most white blood cells of the immune system and are known to modulate the activity of cell signaling receptors via regulatory motifs in their cytoplasmic domains. This immunoglobulin subfamily of coreceptors recognize sialic acid containing glycans as ligands, which are found on glycoproteins and glycolipids of all mammalian cells. By virtue of their ability to recognize this common structural element, siglecs are increasingly recognized for their ability to help immune cells distinguish between self and nonself, and dampen autoimmune responses.

Indexed as

Adaptive ImmunityAutoantigensImmunity, InnateAnimalsHumansLectinsLigandsMiceModels, ImmunologicalPolysaccharidesSialic Acid Binding Immunoglobulin-like LectinsSialic AcidsSignal TransductionToll-Like ReceptorsAutoantigensLectinsLigandsPolysaccharidesSialic Acid Binding Immunoglobulin-like LectinsSialic AcidsToll-Like Receptors

Identifiers

PMID22288608
PMCPMC3335958
OpenAlexW1948372455

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.