Evidence map›Paper›PMID 29246954›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2018

Immunoregulatory Activity of the Natural Product Laminarin Varies Widely as a Result of Its Physical Properties.

Alyson J Smith, Bridget Graves, Robert Child, Peter J Rice, Zuchao Ma, Douglas W Lowman, Harry E Ensley, Kendal T Ryter, Jay T Evans, David L Williams

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
9.6field-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

36 citing papers in PubMed, 83 citations in OpenAlex.

  1. Loss of Fgr41 inInfection and immunity · 2026
    Article
  2. Review
  3. Review
  4. Article
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  6. Review
  7. Article
  8. Article
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  10. Article
  11. Article
  12. Journal of fungi (Basel, Switzerland) · 2024
    Article
  13. Article
  14. Heat-killediScience · 2024
    Article
  15. Review
  16. β-glucans fromFrontiers in nutrition · 2024
    Article
  17. Article
  18. Article
  19. Review
  20. Differential Recognition of Clinically RelevantJournal of fungi (Basel, Switzerland) · 2023
    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

10 authors at 2 institutions in 1 country.

Alyson J SmithDivision of Biological Sciences, University of Montana, Missoula, MT 59812; Alyson.smith@mso.umt.edu.ORCID 0000-0001-8507-6108
Bridget GravesDepartment of Surgery, Quillen College of Medicine, East Tennessee State University, Johnson City, TN 37604.
Robert ChildDivision of Biological Sciences, University of Montana, Missoula, MT 59812.
Peter J RiceCenter of Excellence in Inflammation, Infectious Disease, and Immunity, Quillen College of Medicine, East Tennessee State University, Johnson City, TN 37614.
Zuchao MaDepartment of Surgery, Quillen College of Medicine, East Tennessee State University, Johnson City, TN 37604.ORCID 0000-0001-6363-835X
Douglas W LowmanDepartment of Surgery, Quillen College of Medicine, East Tennessee State University, Johnson City, TN 37604.ORCID 0000-0002-2080-3447
Harry E EnsleyDepartment of Surgery, Quillen College of Medicine, East Tennessee State University, Johnson City, TN 37604.
Kendal T RyterDepartment of Chemistry, University of Montana, Missoula, MT 59812.ORCID 0000-0003-2718-2759
Jay T EvansDivision of Biological Sciences, University of Montana, Missoula, MT 59812.ORCID 0000-0001-6602-0272
David L WilliamsDepartment of Surgery, Quillen College of Medicine, East Tennessee State University, Johnson City, TN 37604.
East Tennessee State University · USUniversity of Montana · US

Funding

Training Innate Immunity: A new approach to the treatment of SepsisR01GM119197 · NIGMS · EAST TENNESSEE STATE UNIVERSITY · PI SHERWOOD, EDWARD R, WILLIAMS, DAVID L. · 2016 to 2024
$4.6M
Innate Immunity and Cardiovascular Function in SepsisR01GM083016 · NIGMS · EAST TENNESSEE STATE UNIVERSITY · PI LI, CHUANFU, WILLIAMS, DAVID L. · 2009 to 2021
$3.8M
AMELIORATION OF SEPSIS BY MACROPHAGE ACTIVATIONR01GM053522 · NIGMS · EAST TENNESSEE STATE UNIVERSITY · PI WILLIAMS, DAVID L. · 1996 to 2015
$3.4M
Integrated Phosphor and Fluorescence Imager (Typhoon FLA9500)S10OD021710 · OD · UNIVERSITY OF MONTANA · PI NUNBERG, JACK H · 2016 to 2016
$138k
NIAID NIH HHS HHSN272201400050CNIGMS NIH HHS R01 GM053522NIGMS NIH HHS R01 GM083016NIGMS NIH HHS R01 GM119197NIH HHS S10 OD021710
6 · The paper itself

Abstract

Ligation of Dectin-1 by fungal glucans elicits a Th17 response that is necessary for clearing many fungal pathogens. Laminarin is a (1→3, 1→6)-β-glucan that is widely reported to be a Dectin-1 antagonist, however, there are reports that laminarin is also a Dectin-1 agonist. To address this controversy, we assessed the physical properties, structure, purity, Dectin-1 binding, and biological activity of five different laminarin preparations from three different commercial sources. The proton nuclear magnetic resonance analysis indicated that all of the preparations contained laminarin although their molecular mass varied considerably (4400-34,400 Da). Two of the laminarins contained substantial quantities of very low m.w. compounds, some of which were not laminarin. These low m.w. moieties could be significantly reduced by extensive dialysis. All of the laminarin preparations were bound by recombinant human Dectin-1 and mouse Dectin-1, but the affinity varied considerably, and binding affinity did not correlate with Dectin-1 agonism, antagonism, or potency. In both human and mouse cells, two laminarins were Dectin-1 antagonists and two were Dectin-1 agonists. The remaining laminarin was a Dectin-1 antagonist, but when the low m.w. moieties were removed, it became an agonist. We were able to identify a laminarin that is a Dectin-1 agonist and a laminarin that is Dectin-1 antagonist, both of which are relatively pure preparations. These laminarins may be useful in elucidating the structure and activity relationships of glucan/Dectin-1 interactions. Our data demonstrate that laminarin can be either a Dectin-1 antagonist or agonist, depending on the physicochemical properties, purity, and structure of the laminarin preparation employed.

Indexed as

AnimalsBiological ProductsCell LineCytokinesDectin-1Gene Knockdown TechniquesGlucansHumansImmunologic FactorsImmunomodulationLectins, C-TypeLeukocytes, MononuclearMacrophagesMicePolymersProtein BindingBiological ProductsCytokinesDectin-1GlucansImmunologic FactorslaminaranLectins, C-TypePolymersRecombinant Proteins

Identifiers

PMID29246954
PMCPMC5760317
OpenAlexW2773495508

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.