Evidence map›Paper›PMID 26519534›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2015

β-Glucan-Activated Human B Lymphocytes Participate in Innate Immune Responses by Releasing Proinflammatory Cytokines and Stimulating Neutrophil Chemotaxis.

Mohamed F Ali, Christopher B Driscoll, Paula R Walters, Andrew H Limper, Eva M Carmona

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

33 citing papers in PubMed, 73 citations in OpenAlex.

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  16. Dietary supplementation of Nile tilapia (Frontiers in veterinary science · 2022
    Article
  17. Update on B Cell Response in Periodontitis.Advances in experimental medicine and biology · 2022
    Article
  18. Article
  19. Review
  20. Evaluation of anFrontiers in microbiology · 2021
    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

5 authors at 1 institution in 1 country.

Mohamed F AliThoracic Diseases Research Unit, Department of Medicine, Mayo Clinic and Foundation, Rochester, MN 55905; and.
Christopher B DriscollThoracic Diseases Research Unit, Department of Medicine, Mayo Clinic and Foundation, Rochester, MN 55905; and.
Paula R WaltersThoracic Diseases Research Unit, Department of Medicine, Mayo Clinic and Foundation, Rochester, MN 55905; and.
Andrew H LimperThoracic Diseases Research Unit, Department of Medicine, Mayo Clinic and Foundation, Rochester, MN 55905; and Division of Pulmonary Critical Care and Internal Medicine, Department of Medicine, Mayo Clinic and Foundation, Rochester, MN 55905.
Eva M CarmonaThoracic Diseases Research Unit, Department of Medicine, Mayo Clinic and Foundation, Rochester, MN 55905; and Division of Pulmonary Critical Care and Internal Medicine, Department of Medicine, Mayo Clinic and Foundation, Rochester, MN 55905 carmona.eva@mayo.edu.
Mayo Clinic · US

Funding

Pneumocystis: Macrophage & Epithelial ActivationR01HL062150 · NHLBI · MAYO CLINIC ROCHESTER · PI ANDREW H LIMPER · 1998 to 2026
$9.2M
Modulation of host immune defense by Pneumocystis beta-glucansK08HL112849 · NHLBI · MAYO CLINIC ROCHESTER · PI CARMONA PORQUERA, EVA MARIA · 2013 to 2017
$712k
NHLBI NIH HHS K08 HL112849NHLBI NIH HHS R01 HL062150NHLBI NIH HHS R01 HL62150
6 · The paper itself

Abstract

B lymphocytes play an essential regulatory role in the adaptive immune response through Ab production during infection. A less known function of B lymphocytes is their ability to respond directly to infectious Ags through stimulation of pattern recognition receptors expressed on their surfaces. β-Glucans are carbohydrates present in the cell wall of many pathogenic fungi that can be detected in the peripheral blood of patients during infection. They have been shown to participate in the innate inflammatory response, as they can directly activate peripheral macrophages and dendritic cells. However, their effect as direct stimulators of B lymphocytes has not been yet fully elucidated. The aim of this study was to examine the molecular mechanisms and cytokine profiles generated following β-glucan stimulation of B lymphocytes, compared with the well-established TLR-9 agonist CpG oligodeoxynucleotide (CpG), and study the participation of β-glucan-stimulated B cells in the innate immune response. In this article, we demonstrate that β-glucan-activated B lymphocytes upregulate proinflammatory cytokines (TNF-α, IL-6, and IL-8). Of interest, β-glucan, unlike CpG, had no effect on B lymphocyte proliferation or IgM production. When compared with CpG (TLR9 agonist), β-glucan-activated cells secreted significantly higher levels of IL-8. Furthermore, IL-8 secretion was partially mediated by Dectin-1 and required SYK, MAPKs, and the transcription factors NF-κB and AP-1. Moreover, we observed that conditioned media from β-glucan-stimulated B lymphocytes elicited neutrophil chemotaxis. These studies suggest that β-glucan-activated B lymphocytes have an important and novel role in fungal innate immune responses.

Indexed as

beta-GlucansB-LymphocytesCell ProliferationChemotaxis, LeukocyteCulture Media, ConditionedDectin-1HumansImmunity, InnateImmunoglobulin MInterleukin-6Interleukin-8Intracellular Signaling Peptides and ProteinsLectins, C-TypeLymphocyte ActivationNeutrophilsNF-kappa Bbeta-GlucansCulture Media, ConditionedCXCL8 protein, humanDectin-1IL6 protein, humanImmunoglobulin MInterleukin-6Interleukin-8Intracellular Signaling Peptides and ProteinsLectins, C-TypeNF-kappa BOligodeoxyribonucleotidesProtein-Tyrosine KinasesSyk KinaseSYK protein, humanTLR9 protein, humanToll-Like Receptor 9Transcription Factor AP-1Tumor Necrosis Factor-alpha

Identifiers

PMID26519534
PMCPMC4655155
OpenAlexW1822463228

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.