Evidence map›Paper›PMID 41813976›Full record

ArticleCommunications medicine2026

hERG epitope mimic-decoy peptide corrects autoimmune-long QT syndrome in guinea pigs.

Michael Cupelli, Vamsi Krishna Murthy Ginjupalli, Jean-Baptiste Reisqs, Yvonne Sleiman, Manuel Becerra-Flores, Riccardo Accioli, Pietro Enea Lazzerini, Timothy Cardozo, Mohamed Boutjdir

Abstract read
In one paragraph

Article in Communications medicine, 2026. 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
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0citing papers in PubMed
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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

9 authors.

Michael Cupelli *Cardiovascular Research Program, VA New York Harbor Healthcare System, New York, NY, USA.
Vamsi Krishna Murthy Ginjupalli *Cardiovascular Research Program, VA New York Harbor Healthcare System, New York, NY, USA.
Jean-Baptiste ReisqsCardiovascular Research Program, VA New York Harbor Healthcare System, New York, NY, USA.ORCID http://orcid.org/0000-0001-9881-6670
Yvonne SleimanCardiovascular Research Program, VA New York Harbor Healthcare System, New York, NY, USA.ORCID http://orcid.org/0000-0002-1550-8945
Manuel Becerra-FloresDepartment of Biochemistry and Molecular Pharmacology, New York University (NYU) Grossman School of Medicine, New York, NY, USA.
Riccardo AccioliDepartment of Medical Sciences, Surgery and Neurosciences, University of Siena, Siena, Italy.
Pietro Enea LazzeriniDepartment of Medical Sciences, Surgery and Neurosciences, University of Siena, Siena, Italy.
Timothy CardozoDepartment of Biochemistry and Molecular Pharmacology, New York University (NYU) Grossman School of Medicine, New York, NY, USA.
Mohamed BoutjdirCardiovascular Research Program, VA New York Harbor Healthcare System, New York, NY, USA. mohamed.boutjdir@va.gov.

Funding

BLRD VA I01 BX002137U.S. Department of Defense (United States Department of Defense) W81XWH-21-1-0424U.S. Department of Health & Human Services | NIH | National Heart, Lung, and Blood Institute (NHLBI) 1R01HL164415
6 · The paper itself

Abstract

backgroundThe most investigated form of autoimmune-long-QT-syndrome (LQTS) is caused by circulating anti-Ro/SSA(Sjögren's syndrome-related antigen-A)-52kD antibodies, which cross-react with a specific sequence of the human ether-à-go-go-related (hERG) potassium channel's pore region, reducing the rapid inward-rectifying potassium current (I

methodsMDP4 was designed using 3D-structure-based protein engineering and optimized via conformational search and energy minimization. QT-interval prolongation was induced in an established guinea pig model of autoimmune-associated LQTS via injection of Ro/SSA-52kD antigen over 15 days. Upon confirmation of QT-interval prolongation, MDP4 was administered, and electrocardiogram parameters were monitored for 30 days. I

resultsGuinea pigs immunized with Ro/SSA-52kD antigen exhibit QTc prolongation and hERG-cross-reactive anti-Ro/SSA-52kD serum antibodies. In vivo treatment with MDP4 reverses QTc prolongation. MDP4 in vitro treatment of guinea pig ventricular myocytes also reverses I

conclusionsTreatment with MDP4 results in recovery of both the QT-interval prolongation in vivo and I

Identifiers

PMID41813976
PMCPMC13111631

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