Evidence map›Paper›PMID 40313754›Full record

ArticleResearch square2025

Single-dose administration of therapeutic divalent siRNA targeting MECP2 prevents lethality for one year in an MECP2 duplication mouse model.

Vignesh N Hariharan, Ashley Summers, Amy E Clipperton-Allen, Jillian Caiazzi, Samuel R Hildebrand, Daniel O' Reilly, Qi Tang, Zachary Kennedy, Dimas Echeverria, Nicholas McHugh and 6 more

Abstract readPreprint
In one paragraph

Article in Research square, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

5 · Who and what money

Authors and funding

16 authors.

Vignesh N HariharanRNA Therapeutic Institute, University of Massachusetts Chan Medical School; Worcester, United States of America.ORCID 0000-0001-9624-1244
Ashley SummersRNA Therapeutic Institute, University of Massachusetts Chan Medical School; Worcester, United States of America.ORCID 0000-0002-5425-0457
Amy E Clipperton-AllenThe Jackson Laboratory; Bar Harbor, United States of America.
Jillian CaiazziRNA Therapeutic Institute, University of Massachusetts Chan Medical School; Worcester, United States of America.
Samuel R HildebrandRNA Therapeutic Institute, University of Massachusetts Chan Medical School; Worcester, United States of America.
Daniel O' ReillyRNA Therapeutic Institute, University of Massachusetts Chan Medical School; Worcester, United States of America.
Qi TangRNA Therapeutic Institute, University of Massachusetts Chan Medical School; Worcester, United States of America.ORCID 0000-0002-8913-0519
Zachary KennedyRNA Therapeutic Institute, University of Massachusetts Chan Medical School; Worcester, United States of America.ORCID 0000-0003-2476-1624
Dimas EcheverriaRNA Therapeutic Institute, University of Massachusetts Chan Medical School; Worcester, United States of America.
Nicholas McHughRNA Therapeutic Institute, University of Massachusetts Chan Medical School; Worcester, United States of America.ORCID 0000-0003-2004-0811
David CooperRNA Therapeutic Institute, University of Massachusetts Chan Medical School; Worcester, United States of America.ORCID 0000-0003-1356-1707
Jacqueline SouzaRNA Therapeutic Institute, University of Massachusetts Chan Medical School; Worcester, United States of America.
Chantal FergusonRNA Therapeutic Institute, University of Massachusetts Chan Medical School; Worcester, United States of America.
Laurent BogdanikThe Jackson Laboratory; Bar Harbor, United States of America.
Monica CoenraadsThe Rett Syndrome Research Trust; Trumbull, United States of America.
Anastasia KhvorovaRNA Therapeutic Institute, University of Massachusetts Chan Medical School; Worcester, United States of America.ORCID 0000-0001-6928-8071

Funding

Expanding the chemical diversity of therapeutic oligonucleotides to treat neurodegenerative disordersR01NS104022 · NINDS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI ANASTASIA KHVOROVA · 2017 to 2026
$6.0M
Development of RNAi based sFLT1-targeting therapeutics for treatment of PreeclampsiaR01HD086111 · NICHD · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI KHVOROVA, ANASTASIA · 2016 to 2020
$3.4M
Mid-Scale RNA Synthesis, Purification and Quality Control SystemS10OD020012 · OD · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI KHVOROVA, ANASTASIA · 2015 to 2015
$563k
NICHD NIH HHS R01 HD086111NIH HHS S10 OD020012NINDS NIH HHS R01 NS104022
6 · The paper itself

Abstract

MECP2 duplication syndrome (MDS) is a rare X-linked neurodevelopmental disorder caused by duplications of the dosage-sensitive methyl-CpG-binding protein 2 (MECP2) gene. Developing effective therapies for MDS is particularly challenging due to the variability in MECP2 expression among patients and the potential risk of inducing Rett syndrome through excessive pharmacological intervention. Reducing dosage to optimize silencing levels often compromises durability and necessitates increased dosing frequency. We present here a series of fully chemically modified small interfering RNAs (siRNAs) designed for both isoform-selective and total MECP2 silencing. Among these, we identify six lead siRNA candidates across two distinct chemical scaffolds, achieving targeted total MECP2 expression reductions ranging from 25% to 75%, sustained for at least four months following a single administration. The efficacy and safety of human ortholog silencing were evaluated using two mouse models with distinct levels of human MECP2 transgene expression. In the severe duplication model, a single dose of the total isoform-silencing siRNA fully rescued early mortality and behavioral impairments. Additionally, we show that the isoform-selective targeting strategy may be safer in mild cases of MDS where exaggerated pharmacology may lead to Rett Syndrome. Overall, this study introduces a series of preclinical candidates with the capacity to address the varying levels of MECP2 duplication encountered in clinical settings. Furthermore, it establishes a target selection strategy that may be applied to other dosage-sensitive gene imbalances.

Identifiers

PMID40313754
PMCPMC12045366

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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 OpenQuestion graph.