Evidence map›Paper›PMID 35203650›Full record

ArticleBiomedicines2022

Gut Microbiota-Derived Small Extracellular Vesicles Endorse Memory-like Inflammatory Responses in Murine Neutrophils.

Trim Lajqi, Natascha Köstlin-Gille, Stefan Hillmer, Maylis Braun, Simon A Kranig, Stefanie Dietz, Christian Krause, Jessica Rühle, David Frommhold, Johannes Pöschl and 2 more

Open access · goldAbstract read
In one paragraph

Article in Biomedicines, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
4.3field-weighted citation impact, top 4% 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

34 citing papers in PubMed, 42 citations in OpenAlex.

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  17. An approach to evaluate the effect of inflammatory microvesicles on CaExperimental biology and medicine (Maywood, N.J.) · 2025
    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

12 authors at 3 institutions in 1 country.

Trim LajqiDepartment of Neonatology, Heidelberg University Children's Hospital, D-69120 Heidelberg, Germany.ORCID 0000-0002-2584-589X
Natascha Köstlin-GilleDepartment of Neonatology, Heidelberg University Children's Hospital, D-69120 Heidelberg, Germany.ORCID 0000-0003-3718-5507
Stefan HillmerElectron Microscopy Core Facility (EMCF), University of Heidelberg, D-69120 Heidelberg, Germany.
Maylis BraunDepartment of Neonatology, Heidelberg University Children's Hospital, D-69120 Heidelberg, Germany.
Simon A KranigDepartment of Neonatology, Heidelberg University Children's Hospital, D-69120 Heidelberg, Germany.
Stefanie DietzDepartment of Neonatology, Heidelberg University Children's Hospital, D-69120 Heidelberg, Germany.
Christian KrauseDepartment of Neonatology, Heidelberg University Children's Hospital, D-69120 Heidelberg, Germany.
Jessica RühleDepartment of Neonatology, University of Tübingen, D-72076 Tübingen, Germany.
David FrommholdKlinik für Kinderheilkunde und Jugendmedizin, D-87700 Memmingen, Germany.
Johannes PöschlDepartment of Neonatology, Heidelberg University Children's Hospital, D-69120 Heidelberg, Germany.
Christian GilleDepartment of Neonatology, Heidelberg University Children's Hospital, D-69120 Heidelberg, Germany.
Hannes HudallaDepartment of Neonatology, Heidelberg University Children's Hospital, D-69120 Heidelberg, Germany.
Heidelberg University · DEUniversity of Tübingen · DEZentrum für Kinderheilkunde · DE

Funding

Deutsche Forschungsgemeinschaft 01GL1746E
6 · The paper itself

Abstract

Neutrophils are classically characterized as merely reactive innate effector cells. However, the microbiome is known to shape the education and maturation process of neutrophils, improving their function and immune-plasticity. Recent reports demonstrate that murine neutrophils possess the ability to exert adaptive responses after exposure to bacterial components such as LPS (Gram-negative bacteria) or LTA (Gram-positive bacteria). We now ask whether small extracellular vesicles (EVs) from the gut may directly mediate adaptive responses in neutrophils in vitro. Murine bone marrow-derived neutrophils were primed in vitro by small EVs of high purity collected from colon stool samples, followed by a second hit with LPS. We found that low-dose priming with gut microbiota-derived small EVs enhanced pro-inflammatory sensitivity as indicated by elevated levels of TNF-α, IL-6, ROS and MCP-1 and increased migratory and phagocytic activity. In contrast, high-dose priming resulted in a tolerant phenotype, marked by increased IL-10 and decreased transmigration and phagocytosis. Alterations in TLR2/MyD88 as well as TLR4/MyD88 signaling were correlated with the induction of adaptive cues in neutrophils in vitro. Taken together, our study shows that small EVs from stools can drive adaptive responses in neutrophils in vitro and may represent a missing link in the gut-immune axis.

Indexed as

inflammationmemory-likemicrobiotaneutrophilsphagocytosisprimingsmall EVstransmigration

Identifiers

PMID35203650
PMCPMC8962420
OpenAlexW4213308235

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.