Evidence map›Paper›PMID 39286259›Full record

ReviewFrontiers in immunology2024

The anti-inflammatory and tolerogenic potential of small spleen peptides.

Viktor Wixler, Igor Z Zaytsev, Yvonne Boergeling, Stephan Ludwig

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Viktor WixlerInstitute of Molecular Virology, Centre for Molecular Biology of Inflammation, Westfaelische Wilhelms-University, Muenster, Germany.
Igor Z ZaytsevInstitute of Pharmaceutical Technologies, Moscow, Russia.
Yvonne BoergelingInstitute of Molecular Virology, Centre for Molecular Biology of Inflammation, Westfaelische Wilhelms-University, Muenster, Germany.
Stephan LudwigInstitute of Molecular Virology, Centre for Molecular Biology of Inflammation, Westfaelische Wilhelms-University, Muenster, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Maintaining peripheral immune tolerance and preventing harmful autoimmune reactions is a fundamental task of the immune system. However, these essential functions are significantly compromised during autoimmune disorders, creating a major challenge in treating these conditions. In this context, we provide an overview of research on small spleen polypeptides (SSPs) that naturally regulate peripheral immune tolerance. Alongside outlining the observed effects of SSPs, we summarize here the findings on the cellular and molecular mechanisms that underlie their regulatory impact. Specifically, SSPs have demonstrated remarkable effectiveness in halting the progression of developing or established autoimmune disorders like psoriasis or arthritis in animal models. They primarily target dendritic cells (DCs), swiftly prompting the production of extracellular ATP, which is then degraded and sensed by adenosine receptors. This process triggers the mTOR signaling cascade, similar to powerful immune triggers, but instead of a rapid and intense reaction, it leads to a moderate yet significant activation of the mTOR signaling cascade. This induces a tolerogenic state in dendritic cells, ultimately leading to the generation of Foxp3

Indexed as

Immune ToleranceSpleenAnimalsAnti-Inflammatory AgentsAutoimmune DiseasesDendritic CellsHumansPeptidesSignal TransductionT-Lymphocytes, RegulatoryTOR Serine-Threonine KinasesAnti-Inflammatory AgentsPeptidesTOR Serine-Threonine Kinasesadenosinedendritic cellsextracellular ATPmTOR signaling cascadeperipheral immune tolerancetolerogenesis, immunogenesisTreg cells

Identifiers

PMID39286259
PMCPMC11402738

What Socratic holds

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Registered trials

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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 Socratic graph.