Evidence map›Paper›PMID 38993865›Full record

ArticleFrontiers in transplantation2023

AAV9-mediated gene delivery to liver grafts during static cold storage in a rat liver transplant model.

Qimeng Gao, Samuel J Kesseli, Trevor Gonzalez, Min Zhang, Riley Kahan, Madison Krischak, Samantha E Halpern, Mingqing Song, Hongzhi Xu, Nader Abraham and 5 more

Abstract read
In one paragraph

Article in Frontiers in transplantation, 2023. 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
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

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

15 authors.

Qimeng Gao *Department of Surgery, Duke University Medical Center, Durham, NC, United States.
Samuel J Kesseli *Department of Surgery, Duke University Medical Center, Durham, NC, United States.
Trevor GonzalezDepartment of Molecular Genetics & Microbiology, Duke University School of Medicine, Durham, NC, United States.
Min ZhangDepartment of Surgery, Duke University Medical Center, Durham, NC, United States.
Riley KahanDepartment of Surgery, Duke University Medical Center, Durham, NC, United States.
Madison KrischakDepartment of Surgery, Duke University Medical Center, Durham, NC, United States.
Samantha E HalpernDepartment of Surgery, Duke University Medical Center, Durham, NC, United States.
Mingqing SongDepartment of Surgery, Duke University Medical Center, Durham, NC, United States.
Hongzhi XuDepartment of Pathology, Duke University Medical Center, Durham, NC, United States.
Nader AbrahamDepartment of Surgery, Duke University Medical Center, Durham, NC, United States.
Imran J AnwarDepartment of Surgery, Duke University Medical Center, Durham, NC, United States.
Isaac AldereteDepartment of Surgery, Duke University Medical Center, Durham, NC, United States.
Aravind AsokanDepartment of Surgery, Duke University Medical Center, Durham, NC, United States.
Matthew G HartwigDivision of Cardiothoracic Surgery, Department of Surgery, Duke University Medical Center, Durham, NC, United States.
Andrew S BarbasDepartment of Surgery, Duke University Medical Center, Durham, NC, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Recombinant adeno-associated virus (rAAV) is a novel strategy used clinically for gene delivery, but has not been characterized in the context of organ transplantation. We sought to determine the efficacy of rAAV-mediated gene delivery during static cold storage (SCS) prior to liver transplantation. Methods: A triple-plasmid transfection protocol was used to produce rAAV subtype-9 vectors containing firefly luciferase genomes in HEK293 cells. Lewis rat liver grafts were flushed and stored in cold HTK solution. Three experimental groups received rAAV at different doses, administered via the portal vein as a bolus during SCS. A control group did not receive rAAV ( Results: Control animals demonstrated no bioluminescent activity, while animals receiving rAAV-treated livers had increasing bioluminescence, peaking at four weeks but sustained to the eight-week endpoint. This result was confirmed by experimental endpoint tissue luciferase activity assay. Discussion: rAAV mediates gene transduction in liver grafts when administered during SCS and has potential for gene therapy applications in solid organ transplantation.

Indexed as

adeno-associated virusgene therapyliver transplantratstatic cold storage

Identifiers

PMID38993865
PMCPMC11235296

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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.