Evidence map›Paper›PMID 19076345›Full record

ReviewAnnals of the New York Academy of Sciences2008

Basic and clinical immunology of Siglecs.

Stephan von Gunten, Bruce S Bochner

Abstract readReview
In one paragraph

Review in Annals of the New York Academy of Sciences, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 88 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
88citing papers in PubMed, 1 pooled it
3.7field-weighted citation impact, top 6% 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

88 citing papers in PubMed, 1 synthesis or guideline pooled it, 164 citations in OpenAlex.

  1. Pooled it
  2. Increased Frequency of Dysfunctional Siglec-7Frontiers in immunology · 2021
    Trial
  3. Review
  4. Article
  5. Review
  6. Article
  7. Mass cytometric analysis of circulating monocyte subsets in a murine model of diabetic gastroparesis.American journal of physiology. Gastrointestinal and liver physiology · 2025
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Review
  20. Review

28 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.

Stephan von GuntenDepartment of Medicine, Division of Allergy and Clinical Immunology, The Johns Hopkins University School of Medicine, Johns Hopkins Asthma and Allergy Center, Baltimore, MD 21224-6821, USA.
Bruce S Bochner
Johns Hopkins University · US

Funding

Targeting Siglec-8/Siglec-F Reduce Allergic Responses In Vitro and In VivoR01AI072265 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI BOCHNER, BRUCE S · 2007 to 2017
$3.9M
INTEGRINS AND CHEMOKINES IN ALLERGIC CELL RECRUITMENTR01AI041472 · NIAID · JOHNS HOPKINS UNIVERSITY · PI BOCHNER, BRUCE S · 1998 to 2007
$2.5M
Targeting Siglec-8/-F to treat eosinophil and mast cell related disordersR56AI072265 · NIAID · JOHNS HOPKINS UNIVERSITY · PI BOCHNER, BRUCE S · 2012 to 2012
$405k
INTEGRINS AND CHEMOKINES IN ALLERGIC CELL RECRUITMENTR21AI041472 · NIAID · JOHNS HOPKINS UNIVERSITY · PI BOCHNER, BRUCE S · 1997 to 2003
$92k
NIAID NIH HHS AI41472NIAID NIH HHS AI72265NIAID NIH HHS R01 AI041472NIAID NIH HHS R01 AI072265NIAID NIH HHS R21 AI041472NIAID NIH HHS R56 AI072265
6 · The paper itself

Abstract

Siglecs are cell-surface proteins found primarily on hematopoietic cells. By definition, they are members of the immunoglobulin gene super-family and bind sialic acid. Most contain cytoplasmic tyrosine motifs implicated in cell signaling. This review will first summarize characteristics common and unique to Siglecs, followed by a discussion of each human Siglec in numerical order, mentioning in turn its closest murine ortholog or paralog. Each section will describe its pattern of cellular expression, latest known immune functions, ligands, and signaling pathways, with the focus being predominantly on CD33-related Siglecs. Potential clinical and therapeutic implications of each Siglec will also be covered.

Indexed as

AnimalsAntigens, CDAntigens, Differentiation, MyelomonocyticHumansLectinsN-Acetylneuraminic AcidReceptors, ImmunologicSialic Acid Binding Ig-like Lectin 2Sialic Acid Binding Ig-like Lectin 3Sialic Acid Binding Immunoglobulin-like LectinsSignal TransductionAntigens, CDAntigens, Differentiation, MyelomonocyticCD33 protein, humanLectinsN-Acetylneuraminic AcidReceptors, ImmunologicSialic Acid Binding Ig-like Lectin 2Sialic Acid Binding Ig-like Lectin 3Sialic Acid Binding Immunoglobulin-like Lectins

Identifiers

PMID19076345
PMCPMC3902170
OpenAlexW2066248629

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.