Evidence map›Paper›PMID 35211683›Full record

ArticleCritical care explorations2022

Zonulin Antagonist, Larazotide (AT1001), As an Adjuvant Treatment for Multisystem Inflammatory Syndrome in Children: A Case Series.

Lael M Yonker, Zoe Swank, Tal Gilboa, Yasmeen Senussi, Victoria Kenyon, Lena Papadakis, Brittany P Boribong, Ryan W Carroll, David R Walt, Alessio Fasano

Open access · goldAbstract read
In one paragraph

Article in Critical care explorations, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
5.0field-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

15 citing papers in PubMed, 24 citations in OpenAlex.

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  11. COVID-19 and Gut Injury.Nutrients · 2022
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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

10 authors at 4 institutions in 2 countries.

Lael M YonkerMucosal Immunology and Biology Research Center, Massachusetts General Hospital, Boston, MA.
Zoe SwankHarvard Medical School, Boston, MA.
Tal GilboaHarvard Medical School, Boston, MA.
Yasmeen SenussiHarvard Medical School, Boston, MA.
Victoria KenyonMucosal Immunology and Biology Research Center, Massachusetts General Hospital, Boston, MA.
Lena PapadakisDepartment of Pediatrics, Massachusetts General Hospital, Boston, MA.
Brittany P BoribongMucosal Immunology and Biology Research Center, Massachusetts General Hospital, Boston, MA.
Ryan W CarrollDepartment of Pediatrics, Massachusetts General Hospital, Boston, MA.
David R WaltHarvard Medical School, Boston, MA.
Alessio FasanoMucosal Immunology and Biology Research Center, Massachusetts General Hospital, Boston, MA.
Massachusetts General Hospital · USHarvard University · USBrigham and Women's Hospital · USEuropean Biomedical Research Institute of Salerno · IT

Funding

Mechanistically Disentangling the Infected, Inflamed LungK08HL143183 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI YONKER, LAEL · 2018 to 2022
$869k
NHLBI NIH HHS K08 HL143183
6 · The paper itself

Abstract

objectivesA recent study suggests that Multisystem Inflammatory Syndrome in Children (MIS-C) is triggered by gastrointestinal breach of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) viral particles from the gut lumen into systemic circulation. The virus remains in the gut weeks to months after respiratory infection, causing zonulin release from the intestinal epithelial cells. Zonulin loosens tight junctions, permitting trafficking of highly inflammatory viral particles into circulation. Current MIS-C treatments target the subsequent immune hyperactivation, not the causative loss of mucosal barrier integrity. Larazotide, a zonulin inhibitor, prevents breakdown of tight junctions, limiting antigen trafficking.

designChildren with MIS-C were treated with larazotide as an adjuvant to steroid/intravenous immunoglobulin therapy. Clinical outcomes, SARS-CoV-2 antigenemia, and cytokine profiles are reported. Outcomes were compared with children with MIS-C receiving steroids and/or IVIG therapy alone. PATIENTS: Four children with MIS-C, ages 3-17 years, were enrolled.

interventionsPatients were treated with open label larazotide 10 mcg/kg (maximum 500 mcg/dose) orally four times daily for 21 days. MEASUREMENTS AND MAIN

resultsAll four patients tolerated larazotide without adverse effects and displayed reduction in Spike antigenemia to undetectable levels. When compared with 22 children with MIS-C receiving steroids and/or intravenous immunoglobulin therapy alone, larazotide-treated patients reported significantly improved time to resolution of gastrointestinal symptoms (

conclusionsLarazotide appears safe and well-tolerated and may offer potential benefit as an adjuvant to immune-targeted therapies. Expansion of clinical trials is urgently needed to ascertain the clinical impact of larazotide on MIS-C.

Indexed as

AT1001larazotidemultisystem inflammatory syndrome in childrensevere acute respiratory syndrome coronavirus 2 antigenemia

Identifiers

PMID35211683
PMCPMC8860335
OpenAlexW4213344770

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.