Evidence map›Paper›PMID 28888781›Full record

ArticleThe Journal of allergy and clinical immunology2018

Sialic acid-binding immunoglobulin-like lectin 8 (Siglec-8) is an activating receptor mediating β

Daniela J Carroll, Jeremy A O'Sullivan, David B Nix, Yun Cao, Michael Tiemeyer, Bruce S Bochner

Abstract read
In one paragraph

Article in The Journal of allergy and clinical immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
–field-weighted citation impact
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

32 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Siglecs in allergy and asthma.Molecular aspects of medicine · 2023
    Review
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  7. Review
  8. Article
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  15. Review
  16. An anti-siglec-8 antibody depletes sputum eosinophils from asthmatic subjects and inhibits lung mast cells.Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology · 2020
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  17. Article
  18. Review
  19. Article
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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

6 authors.

Daniela J CarrollDepartment of Medicine, Division of Allergy and Immunology, Northwestern University Feinberg School of Medicine, Chicago, Ill.
Jeremy A O'SullivanDepartment of Medicine, Division of Allergy and Immunology, Northwestern University Feinberg School of Medicine, Chicago, Ill.
David B NixComplex Carbohydrate Research Center, University of Georgia, Athens, Ga.
Yun CaoDepartment of Medicine, Division of Allergy and Immunology, Northwestern University Feinberg School of Medicine, Chicago, Ill.
Michael TiemeyerComplex Carbohydrate Research Center, University of Georgia, Athens, Ga.
Bruce S BochnerDepartment of Medicine, Division of Allergy and Immunology, Northwestern University Feinberg School of Medicine, Chicago, Ill. Electronic address: bruce.bochner@northwestern.edu.

Funding

Treating lung inflammation by targeting SiglecsP01HL107151 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI SCHNAAR, RONALD L · 2011 to 2017
$15.4M
TR&D1: Stem Cell and Induced Pluripotent Stem Cell Resources (Pages 116-134)P41GM103490 · NIGMS · UNIVERSITY OF GEORGIA · PI PIERCE, J. MICHAEL · 2012 to 2018
$13.7M
Using siglecs and their ligands to treat allergic diseases SALTADU19AI136443 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI SCHNAAR, RONALD L · 2018 to 2022
$7.6M
Northwestern University Allergy Immunology Research Program (NUAIR)T32AI083216 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Stephanie Caroline Eisenbarth, ADAM WILLIAMS · 2010 to 2026
$4.1M
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
NHLBI NIH HHS P01 HL107151NIAID NIH HHS R01 AI041472NIAID NIH HHS R01 AI072265NIAID NIH HHS R56 AI072265NIAID NIH HHS T32 AI083216NIAID NIH HHS U19 AI136443NIGMS NIH HHS P41 GM103490
6 · The paper itself

Abstract

backgroundSiglec-8 is a CD33 subfamily cell-surface receptor selectively expressed on human eosinophils. After cytokine priming, Siglec-8 mAb or glycan ligand binding causes eosinophil apoptosis associated with reactive oxygen species (ROS) production. Most CD33-related Siglecs function as inhibitory receptors, but the ability of Siglec-8 to stimulate eosinophil ROS production and apoptosis suggests that Siglec-8 might instead function as an activating receptor.

objectiveWe sought to determine the role of IL-5 priming and identify the signaling molecules involved in Siglec-8 function for human eosinophils.

methodsWe used an mAb and/or a multimeric synthetic sulfated sialoglycan ligand recognizing Siglec-8 in combination with integrin blocking antibodies, pharmacologic inhibitors, phosphoproteomics, and Western blot analysis to define the necessity of various proteins involved in Siglec-8 function for human eosinophils.

resultsCytokine priming was required to elicit the unanticipated finding that Siglec-8 engagement promotes rapid β

conclusionsThese data demonstrate that Siglec-8 functions uniquely as an activating receptor on IL-5-primed eosinophils through a novel pathway involving regulation of β

Indexed as

Antigens, CDAntigens, Differentiation, B-LymphocyteApoptosisCD18 AntigensCell AdhesionCell DegranulationEosinophilsHumansLectinsReactive Oxygen SpeciesAntigens, CDAntigens, Differentiation, B-LymphocyteCD18 AntigensLectinsReactive Oxygen SpeciesSIGLEC8 protein, humanAktapoptosisc-Jun N-terminal kinase (JNK)Eosinophilp38phosphoproteomicsreduced nicotinamide adenine dinucleotide phosphate oxidase (NADPH)Siglec-8β(2)-integrin

Identifiers

PMID28888781
PMCPMC5839929

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Registered trials

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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.