Evidence map›Paper›PMID 27933310›Full record

ArticleMolecular therapy. Methods & clinical development2016

Dynamics of antigen presentation to transgene product-specific CD4

George Q Perrin, Irene Zolotukhin, Alexandra Sherman, Moanaro Biswas, Ype P de Jong, Cox Terhorst, Andrew M Davidoff, Roland W Herzog

Open access · goldAbstract read
In one paragraph

Article in Molecular therapy. Methods & clinical development, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 1 pooled it
5.4field-weighted citation impact, top 4% 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

32 citing papers in PubMed, 1 synthesis or guideline pooled it, 37 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Role of FoxP3Human gene therapy · 2024
    Review
  5. Article
  6. Single-dose AAV vector gene immunotherapy to treat food allergy.Molecular therapy. Methods & clinical development · 2022
    Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Review
  12. Immune Response Mechanisms against AAV Vectors in Animal Models.Molecular therapy. Methods & clinical development · 2020
    Review
  13. Article
  14. Immune Responses to Viral Gene Therapy Vectors.Molecular therapy : the journal of the American Society of Gene Therapy · 2020
    Review
  15. AAV Vector Immunogenicity in Humans: A Long Journey to Successful Gene Transfer.Molecular therapy : the journal of the American Society of Gene Therapy · 2020
    Review
  16. Review
  17. Article
  18. Review
  19. Review
  20. Review
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.

George Q PerrinDepartment of Pediatrics, University of Florida , Gainesville, Florida, USA.
Irene ZolotukhinDepartment of Pediatrics, University of Florida , Gainesville, Florida, USA.
Alexandra ShermanDepartment of Pediatrics, University of Florida , Gainesville, Florida, USA.
Moanaro BiswasDepartment of Pediatrics, University of Florida , Gainesville, Florida, USA.
Ype P de JongDivision of Gastroenterology and Hepatology, Weill Cornell Medicine , New York, New York, USA.
Cox TerhorstDivision of Immunology, Beth Israel Deaconess Medical Center, Harvard Medical School , Boston, Massachusetts, USA.
Andrew M DavidoffDepartment of Surgery, St. Jude Children's Research Hospital , Memphis, Tennessee, USA.
Roland W HerzogDepartment of Pediatrics, University of Florida , Gainesville, Florida, USA.
University of Florida · USHarvard University · USSt. Jude Children's Research Hospital · USWeill Cornell Medicine · US

Funding

Enhancing immune regulation in gene therapy for hemophiliaR01HL131093 · NHLBI · UNIVERSITY OF FLORIDA · PI Ype Peter De Jong, Roland W. Herzog · 2016 to 2026
$7.2M
Immunology of Factor IX Gene Transfer to LiverR01AI051390 · NIAID · UNIVERSITY OF FLORIDA · PI HERZOG, ROLAND W. · 2002 to 2022
$6.7M
Next Generation of Recombinant AAV Serotype Vectors for Gene TherapyR01HL097088 · NHLBI · UNIVERSITY OF FLORIDA · PI GAO, GUANGPING, HERZOG, ROLAND W. · 2010 to 2018
$5.4M
rAAV-Mediated Gene Therapy for Hemophillia BR01HL073838 · NHLBI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI DAVIDOFF, ANDREW M · 2005 to 2015
$4.5M
NHLBI NIH HHS R01 HL073838NHLBI NIH HHS R01 HL097088NHLBI NIH HHS R01 HL131093NIAID NIH HHS R01 AI051390
6 · The paper itself

Abstract

The tolerogenic hepatic microenvironment impedes clearance of viral infections but is an advantage in viral vector gene transfer, which often results in immune tolerance induction to transgene products. Although the underlying tolerance mechanism has been extensively studied, our understanding of antigen presentation to transgene product-specific CD4

Identifiers

PMID27933310
PMCPMC5142511
OpenAlexW2560645882

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.