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Study · Not a test of the peptide alone · 2025

3 results

Reprogramming of Treg cell-derived small extracellular vesicles effectively prevents intestinal inflammation from PANoptosis by blocking mitochondrial oxidative stress.

Gong W, Liu Z, Wang Y, Huang W, Yang K, Gao Z, Guo K, Xiao Z, Zhao W

Trends in biotechnology16 Dec 2024Cited by 22 (Europe PMC)

Summary

The text of this summary is not shown here, because the article license does not allow reuse. Read it at the source (opens in a new tab)

Text rights: Publisher copyright. Results still quote short attributed sentences.

Results from this study3

No result from this study comes from a test of the peptide.

Studies that did not test the peptide alone3

In this study, Elamipretide (SS-31) was a lab tool or a carrier, part of a mix, or the subject of a lab method. These results are not evidence about taking Elamipretide (SS-31).

  1. 01AnimalNot a test of Elamipretide (SS-31) aloneAnimal study (in vivo)Efficacy outcome

    A selenium-loaded, SS‑31-decorated Treg exosome delivery system protected against intestinal inflammation.

    In plain wordsAn engineered exosome carrying selenium and SS‑31 protected against gut inflammation. The abstract does not name the model.

    Outcome
    DecreaseIntestinal inflammation
    Study

    n: not reported in source

    Outcome group
    Inflammation markers · Gastrointestinal

    Source sentences

    Summary
    This actively targetable exosome-derived delivery system is protected from intestinal inflammation by scavenging excessive mtROS and preventing immunologically programmed cell death pyroptosis, necroptosis, and apoptosis, known as PANoptosis.
    1 context sentence
    Summary · context
    Here, we reprogrammed regulatory T cell (Treg)-derived exosomes loaded with the antioxidant trace element selenium (Se) and decorated them with the synthetic mitochondria-targeting SS-31 tetrapeptide via a peptide linker.

    In this study, Elamipretide (SS-31) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Elamipretide (SS-31).

  2. 02AnimalNot a test of Elamipretide (SS-31) aloneAnimal study (in vivo)Mechanism

    A selenium-loaded, SS‑31-decorated Treg exosome delivery system scavenged excessive mitochondrial ROS.

    In plain wordsAn engineered exosome carrying selenium and SS‑31 removed excess harmful mitochondrial oxygen molecules.

    Outcome
    DecreaseMitochondrial ROS
    Study

    n: not reported in source

    Outcome group
    Oxidative stress · Gastrointestinal

    Source sentences

    Summary
    scavenging excessive mtROS and preventing immunologically programmed cell death pyroptosis, necroptosis, and apoptosis, known as PANoptosis.
    1 context sentence
    Summary · context
    Here, we reprogrammed regulatory T cell (Treg)-derived exosomes loaded with the antioxidant trace element selenium (Se) and decorated them with the synthetic mitochondria-targeting SS-31 tetrapeptide via a peptide linker.

    In this study, Elamipretide (SS-31) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Elamipretide (SS-31).

  3. 03AnimalNot a test of Elamipretide (SS-31) aloneAnimal study (in vivo)Mechanism

    A selenium-loaded, SS‑31-decorated Treg exosome delivery system prevented PANoptosis (pyroptosis, necroptosis and apoptosis).

    In plain wordsAn engineered exosome carrying selenium and SS‑31 prevented a form of programmed cell death.

    Outcome
    DecreasePANoptosis (pyroptosis, necroptosis, apoptosis)
    Study

    n: not reported in source

    Outcome group
    Inflammation markers · Gastrointestinal

    Source sentences

    Summary
    preventing immunologically programmed cell death pyroptosis, necroptosis, and apoptosis, known as PANoptosis.
    1 context sentence
    Summary · context
    Here, we reprogrammed regulatory T cell (Treg)-derived exosomes loaded with the antioxidant trace element selenium (Se) and decorated them with the synthetic mitochondria-targeting SS-31 tetrapeptide via a peptide linker.

    In this study, Elamipretide (SS-31) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Elamipretide (SS-31).

AI wrote and checked these results. AI can make mistakes, so check important results against the source.

Version history

PepBank keeps every version of the data on this study. Status changes from Retraction Watch, Europe PMC and Crossref are listed with their source.

  1. Version 2Current

    10 Oct 2026, 08:19 UTC

    Study results updated

  2. Version 1

    9 Oct 2026, 02:47 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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