Evidence map›Paper›PMID 21208791›Full record

ReviewCurrent opinion in immunology2011

Sialoside-based pattern recognitions discriminating infections from tissue injuries.

Yang Liu, Guo-Yun Chen, Pan Zheng

Registry-linked trialOpen access · greenAbstract readReview
In one paragraph

Review in Current opinion in immunology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04317040 (A Randomized, Double-blind, Placebo-controlled, Multi-site, Phase III Study to Evaluate the Safety and Efficacy of CD24Fc in COVID-19 Treatment), which is not on this map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.2field-weighted citation impact, top 22% 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.

NCT04317040 phase3completednot on this mapstarted 2020, after this paper: background citation

A Randomized, Double-blind, Placebo-controlled, Multi-site, Phase III Study to Evaluate the Safety and Efficacy of CD24Fc in COVID-19 Treatment

TypeinterventionalSponsorOncoimmune, Inc., a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA)Ran2020 to 2020Enrolled234ConditionsCoronavirus Disease 2019 (COVID-19)ArmsEfprezimod alfa, Placebo
3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
  2. Review
  3. Impact of Siglecs on autoimmune diseases.Molecular aspects of medicine · 2023
    Review
  4. Review
  5. Article
  6. CD24: A Novel Target for Cancer Immunotherapy.Journal of personalized medicine · 2022
    Review
  7. Article
  8. Article
  9. Biological roles of glycans.Glycobiology · 2017
    Review
  10. Review
  11. Article
  12. Endometriosis, a disease of the macrophage.Frontiers in immunology · 2013
    Article
  13. Siglecs as sensors of self in innate and adaptive immune responses.Annals of the New York Academy of Sciences · 2012
    Review
  14. Siglecs and immune regulation.Annual review of immunology · 2012
    Review
  15. 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

3 authors at 1 institution in 1 country.

Yang LiuDivision of Immunotherapy, Department of Surgery, University of Michigan School of Medicine, Ann Arbor, MI 48109, United States. yangl@umich.edu
Guo-Yun Chen
Pan Zheng
University of Michigan–Ann Arbor · US

Funding

Checkpoints of Host Response to Cellular InjuriesR01AI064350 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LIU, YANG, ZHENG, PAN · 2006 to 2019
$5.6M
Tumor burden and T cell immunityR01CA058033 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LIU, YANG · 1992 to 2013
$3.3M
mTOR, Inflammation and Senescence of Hematopoietic Stem CellsR01AG036690 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ZHENG, PAN · 2010 to 2014
$1.6M
CD24 Polymorphism and Acetaminophen ToxicityRC1GM091648 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ZHENG, PAN · 2009 to 2010
$998k
NCI NIH HHS R01 CA058033NIAID NIH HHS R01 AI064350NIA NIH HHS R01 AG036690NIGMS NIH HHS RC1 GM091648
6 · The paper itself

Abstract

Recognition of pathogens-associated molecular patterns (PAMPs) by Toll-like receptors (TLRs), NOD-like receptors (NLRs) and RIG-I-like receptors (RLR) plays a critical role in protecting host against pathogens. In addition, TLR and NLR also recognize danger-associated molecular patterns (DAMPs) to initiate limited innate immune responses. While innate immune response to DAMPs may be important for tissue repairs and wound healing, it is normally well controlled to avoid autoimmune destruction. Recent data support a role for sialoside-based pattern recognition by members of the Siglec family to attenuate innate immunity. In particular, since CD24-Siglec 10/G interaction selectively dampens host response to DAMPs but not PAMPs, this sialoside-based pattern recognition may serve as a foundation to discriminate PAMPs from DAMPs.

Indexed as

AnimalsCD24 AntigenHumansImmunity, InnateInfectionsSugar Acids3-deoxyglycero-galacto-nonulosonic acidCD24 AntigenSugar Acids

Identifiers

PMID21208791
PMCPMC3042481
OpenAlexW2065405440

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.