Evidence map›Paper›PMID 42400303›Full record

ArticleLiver international : official journal of the International Association for the Study of the Liver2026

Adeno-Associated Virus Gene Therapy for Spinal Muscular Atrophy Induces Hepatotoxicity via Cytokine and Macrophage Activation.

Aiko Sakai, Masaya Sugiyama, Masafumi Onodera, Fujiko Fukushima, Mai Tanaka, Toru Uchiyama, Masashi Mizokami, Ryo Sumazaki

Abstract readCase Reports
In one paragraph

Article in Liver international : official journal of the International Association for the Study of the Liver, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Adeno-Associated Virus Gene Therapy for Spinal Muscular Atrophy Induces Hepatotoxicity via Cytokine and Macrophage Activation.Liver international : official journal of the International Association for the Study of the Liver · 2026
    Article
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

8 authors.

Aiko SakaiDepartment of Viral Pathogenesis and Controls, National Institute of Global Health and Medicine, Japan Institute for Health Security, Ichikawa, Chiba, Japan.ORCID 0000-0002-2762-0205
Masaya SugiyamaDepartment of Viral Pathogenesis and Controls, National Institute of Global Health and Medicine, Japan Institute for Health Security, Ichikawa, Chiba, Japan.ORCID 0000-0002-9084-7197
Masafumi OnoderaGene and Cell Therapy Promotion Center, National Center for Child Health and Development, Setagaya-ku, Tokyo, Japan.
Fujiko FukushimaDepartment of Pediatrics, Ibaraki Children's Hospital, Mito, Ibaraki, Japan.
Mai TanakaDepartment of Pediatrics, University of Tsukuba Hospital, Tsukuba, Ibaraki, Japan.
Toru UchiyamaDepartment of Human Genetics, National Center for Child Health and Development, Setagaya-ku, Tokyo, Japan.
Masashi MizokamiGenome Medical Sciences Project, National Center for Global Health and Medicine, Ichikawa, Chiba, Japan.
Ryo SumazakiDepartment of Viral Pathogenesis and Controls, National Institute of Global Health and Medicine, Japan Institute for Health Security, Ichikawa, Chiba, Japan.

Funding

Japan Agency for Medical Research and Development JP22fk0108541
6 · The paper itself

Abstract

Hepatotoxicity is a common and significant adverse effect associated with adeno-associated virus (AAV) gene therapy; however, the underlying mechanisms remain unknown. In this study, we demonstrated innate immune activation in two patients with spinal muscular atrophy shortly after receiving AAV9 gene therapy with onasemnogene abeparvovec. Both patients developed marked hyperferritinemia accompanied by hepatotoxicity, thrombocytopenia, hypertriglyceridemia, and hypofibrinogenemia, all of which are the diagnostic criteria for macrophage activation syndrome. To evaluate their immune responses, serial analyses of serum cytokines/chemokines and flow cytometry were performed. Surges in macrophage-associated cytokine levels were observed in proportion to the severity of adverse events within 1 week after AAV vector infusion, suggesting that macrophage activation contributed to the pathogenesis of these adverse effects. Our findings clarify the immunological basis underlying hepatotoxicity in patients after AAV gene therapy. Furthermore, these findings provide a rationale for using various immunosuppressants or chemokine blockers in patients exhibiting severe adverse effects.

Indexed as

Chemical and Drug Induced Liver InjuryCytokinesDependovirusGenetic TherapyMacrophage ActivationMacrophage Activation SyndromeMuscular Atrophy, SpinalFemaleGene Therapy AgentsGenetic VectorsHumansImmunity, InnateMaleRecombinant Fusion ProteinsCytokinesonasemnogene abeparvovecRecombinant Fusion Proteinsadeno‐associated viruscytokineshyperferritinemiainnate immunity

Identifiers

PMID42400303
PMCPMC13332412

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.