Evidence map›Paper›PMID 37702486›Full record

ArticleJournal of virology2023

Structural and antigenic characterization of the avian adeno-associated virus capsid.

Jane Hsi, Mario Mietzsch, Paul Chipman, Sandra Afione, Allison Zeher, Rick Huang, John Chiorini, Robert McKenna

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

12 citing papers in PubMed, 15 citations in OpenAlex.

  1. Identification of CD164 as an essential entry receptor for divergent adeno-associated viruses.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Article
  3. The amazing AAV capsids: Into the structure-verse.Molecular therapy. Methods & clinical development · 2025
    Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. The Structure ofViruses · 2024
    Article
  11. Genomic loss of GPR108 disrupts AAV transduction in birds.bioRxiv : the preprint server for biology · 2024
    Article
  12. 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 at 4 institutions in 1 country.

Jane HsiDepartment of Biochemistry and Molecular Biology, Center for Structural Biology, McKnight Brain Institute, College of Medicine, University of Florida , Gainesville, Florida, USA.ORCID 0000-0002-0076-4217
Mario MietzschDepartment of Biochemistry and Molecular Biology, Center for Structural Biology, McKnight Brain Institute, College of Medicine, University of Florida , Gainesville, Florida, USA.ORCID 0000-0001-8957-3363
Paul ChipmanDepartment of Biochemistry and Molecular Biology, Center for Structural Biology, McKnight Brain Institute, College of Medicine, University of Florida , Gainesville, Florida, USA.
Sandra AfioneNational Institute of Dental and Craniofacial Research, NIH , Bethesda, Maryland, USA.
Allison ZeherLaboratory of Cell Biology, Center for Cancer Research, National Cancer Institute, NIH , Bethesda, Maryland, USA.
Rick HuangLaboratory of Cell Biology, Center for Cancer Research, National Cancer Institute, NIH , Bethesda, Maryland, USA.
John ChioriniNational Institute of Dental and Craniofacial Research, NIH , Bethesda, Maryland, USA.
Robert McKennaDepartment of Biochemistry and Molecular Biology, Center for Structural Biology, McKnight Brain Institute, College of Medicine, University of Florida , Gainesville, Florida, USA.ORCID 0000-0002-2792-935X
University of Florida · USNational Institute of Dental and Craniofacial Research · USBloomberg (United States) · USNational Cancer Institute · US

Funding

Structural studies of AAV capsids and their glycan receptor interactionsR01GM082946 · NIGMS · UNIVERSITY OF FLORIDA · PI ROBERT MCKENNA · 2007 to 2026
$6.1M
NIGMS NIH HHS R01 GM082946
6 · The paper itself

Abstract

importanceAAVs are extensively studied as promising therapeutic gene delivery vectors. In order to circumvent pre-existing antibodies targeting primate-based AAV capsids, the AAAV capsid was evaluated as an alternative to primate-based therapeutic vectors. Despite the high sequence diversity, the AAAV capsid was found to bind to a common glycan receptor, terminal galactose, which is also utilized by other AAVs already being utilized in gene therapy trials. However, contrary to the initial hypothesis, AAAV was recognized by approximately 30% of human sera tested. Structural and sequence comparisons point to conserved epitopes in the fivefold region of the capsid as the reason determinant for the observed cross-reactivity.

Indexed as

Antigens, ViralCapsidParvovirinaeAnimalsCapsid ProteinsDependovirusGenetic VectorsHumansPrimatesAntigens, ViralCapsid ProteinsAAV vectoradeno-associated virusantigenicityavian virusescapsidcryo-EMgene therapyparvovirusthree-dimensional structure

Identifiers

PMID37702486
PMCPMC10617571
OpenAlexW4386704422

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.