Evidence map›Paper›PMID 19359050›Full record

ReviewTrends in pharmacological sciences2009

Siglecs as targets for therapy in immune-cell-mediated disease.

Mary K O'Reilly, James C Paulson

Open access · greenAbstract readReview
In one paragraph

Review in Trends in pharmacological sciences, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 103 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
103citing papers in PubMed, 1 pooled it
8.2field-weighted citation impact, top 2% 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

103 citing papers in PubMed, 1 synthesis or guideline pooled it, 184 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
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  10. Article
  11. Review
  12. Review
  13. High affinity monoclonal antibody targeting Siglec-15 for cancer immunotherapy.Journal of clinical and translational research · 2021
    Article
  14. Review
  15. Review
  16. Article
  17. First Evidence for a Role of Siglec-8 in Breast Cancer.International journal of molecular sciences · 2021
    Article
  18. Review
  19. Article
  20. Article

43 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.

Mary K O'ReillyDepartment of Chemical Physiology, The Scripps Research Institute, La Jolla CA 92037, USA.
James C Paulson
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
MAMMALIAN SIALIC ACID BINDING PROTEINSR01GM060938 · NIGMS · SCRIPPS RESEARCH INSTITUTE, THE · PI PAULSON, JAMES C · 2000 to 2010
$4.0M
NIAID NIH HHS AI050143NIAID NIH HHS R01 AI050143NIGMS NIH HHS GM060938NIGMS NIH HHS R01 GM060938
6 · The paper itself

Abstract

The sialic-acid-binding immunoglobulin-like lectins (siglecs) comprise a family of receptors that are differentially expressed on leukocytes and other immune cells. The restricted expression of several siglecs to one or a few cell types makes them attractive targets for cell-directed therapies. The anti-CD33 (also known as Siglec-3) antibody gemtuzumab (Mylotarg) is approved for the treatment of acute myeloid leukemia, and antibodies targeting CD22 (Siglec-2) are currently in clinical trials for treatment of B cell non-Hodgkins lymphomas and autoimmune diseases. Because siglecs are endocytic receptors, they are well suited for a 'Trojan horse' strategy, whereby therapeutic agents conjugated to an antibody, or multimeric glycan ligand, bind to the siglec and are efficiently carried into the cell. Although the rapid internalization of unmodified siglec antibodies reduces their utility for induction of antibody-dependent cellular cytotoxicity or complement-mediated cytotoxicity, antibody binding of Siglec-8, Siglec-9 and CD22 has been demonstrated to induce apoptosis of eosinophils, neutrophils and depletion of B cells, respectively. Here, we review the properties of siglecs that make them attractive for cell-targeted therapies.

Indexed as

LectinsAminoglycosidesAnimalsAntibodiesAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedAntigens, CDAntigens, Differentiation, MyelomonocyticClinical Trials as TopicDrug Delivery SystemsGemtuzumabHumansImmune System DiseasesLeukemiaLymphocyte DepletionLymphoma, B-CellAminoglycosidesAntibodiesAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedAntigens, CDAntigens, Differentiation, MyelomonocyticCD33 protein, humanGemtuzumabLectinsPolysaccharidesSialic Acid Binding Ig-like Lectin 2Sialic Acid Binding Ig-like Lectin 3Sialic Acid Binding Immunoglobulin-like Lectins

Identifiers

PMID19359050
PMCPMC2830709
OpenAlexW1993160668

What OpenQuestion holds

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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.