Evidence map›Paper›PMID 18373667›Full record

ArticleImmunology2008

The immunomodulatory glycan LNFPIII initiates alternative activation of murine macrophages in vivo.

Olga Atochina, Akram A Da'dara, Mirjam Walker, Donald A Harn

Open access · bronzeAbstract read
In one paragraph

Article in Immunology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
4.8field-weighted citation impact, top 5% 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

46 citing papers in PubMed, 79 citations in OpenAlex.

  1. Article
  2. Review
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  4. Biology of human milk oligosaccharides: From basic science to clinical evidence.Journal of human nutrition and dietetics : the official journal of the British Dietetic Association · 2022
    Review
  5. Review
  6. Schistosome immunomodulators.PLoS pathogens · 2021
    Review
  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Targeted LC-ESI-MSAnalytical and bioanalytical chemistry · 2020
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. 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

4 authors at 1 institution in 1 country.

Olga AtochinaDepartment of Immunology and Infectious Diseases, Harvard School of Public Health, Boston, MA 02115, USA. oatochin@hsph.harvard.edu
Akram A Da'dara
Mirjam Walker
Donald A Harn
Harvard University · US

Funding

Immune Responses to Schistosome Egg AntigensR01AI056484 · NIAID · UNIVERSITY OF GEORGIA · PI HARN, DONALD A · 2003 to 2010
$2.2M
NIAID NIH HHS 5R01AI056484NIAID NIH HHS R01 AI056484
6 · The paper itself

Abstract

The early pathogen-macrophage interactions that help drive macrophage maturation towards classically or alternatively activated are largely unknown. To examine this question we utilized the immunomodulatory glycan Lacto-N-fucopentaose III (LNFPIII), which contains the Lewis X (LeX) trisaccharide, to activate murine peritoneal macrophages in vivo. Because LNFPIII is known to induce anti-inflammatory responses, we asked if LNFPIII stimulation of macrophages in vivo initiates alternative activation events such as upregulation of Arginase 1, Ym1, FIZZ-1, MGL-1 or macrophage mannose receptor (MMR). Examination of peritoneal exudate cells from mice 20 hr post-LNFPIII injection demonstrated increased Arginase 1 activity, at the mRNA and protein levels, coincident with undetectable inducible nitric oxide synthase expression or nitric oxide production. In addition to Arginase 1, Ym1 expression was also significantly upregulated at 20 and 48 hr after LNFPIII exposure in vivo. However, the expression of FIZZ-1, MGL-1, and MMR was not changed in these macrophages. In an attempt to determine activation requirements for functional activity, we adoptively transferred antigen-pulsed, in vivo LNFPIII activated macrophages into naïve recipients and found that they were capable of triggering recipient T cells to secrete elevated levels of interleukin (IL)-10 and IL-13 compared to mice receiving control macrophages. Together, these data demonstrate that upregulation of expression of Arginase 1 and Ym1 occur very early in activation of macrophages, and can be independent of other alternatively activated (AA) macrophage markers. Importantly, these early events appear to be IL-4/IL-13-independent in our model. In the future we hope to determine if upregulation of these initial AA maturational events is sufficient for these macrophages to exert immunoregulatory activity in vivo.

Indexed as

Adoptive TransferAmino SugarsAnimalsArginaseAscitic FluidBiomarkersCell DifferentiationFemaleImmunologic FactorsInterleukin-13Interleukin-4Macrophage ActivationMacrophages, PeritonealMiceMice, Inbred BALB CPolysaccharidesAmino SugarsArginaseBiomarkersImmunologic FactorsInterleukin-13Interleukin-4lacto-N-fucopentaose IIIPolysaccharides

Identifiers

PMID18373667
PMCPMC2526265
OpenAlexW2069474631

What OpenQuestion holds

Textmetadata
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.