Evidence map›Paper›PMID 23790242›Full record

ArticleHuman gene therapy. Clinical development2013

Self-reactive CFTR T cells in humans: implications for gene therapy.

Roberto Calcedo, Uta Griesenbach, Daniel J Dorgan, Samia Soussi, A Christopher Boyd, Jane C Davies, Tracy E Higgins, Stephen C Hyde, Deborah R Gill, J Alastair Innes and 4 more

Open access · greenAbstract readValidation Study
In one paragraph

Article in Human gene therapy. Clinical development, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 36% 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

3 citing papers in PubMed, 9 citations in OpenAlex.

  1. Class I-restricted T-cell responses to a polymorphic peptide in a gene therapy clinical trial for α-1-antitrypsin deficiency.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Trial
  2. Review
  3. The Future of In Utero Gene Therapy.Molecular diagnosis & therapy · 2020
    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

14 authors at 4 institutions in 2 countries.

Roberto Calcedo1 Gene Therapy Program, Department of Pathology and Laboratory Medicine, University of Pennsylvania , Philadelphia, PA 19104.
Uta Griesenbach
Daniel J Dorgan
Samia Soussi
A Christopher Boyd
Jane C Davies
Tracy E Higgins
Stephen C Hyde
Deborah R Gill
J Alastair Innes
David J Porteous
Eric W Alton
James M Wilson
Maria P Limberis
Cystic Fibrosis Trust · GBUniversity of Pennsylvania · USWestern General Hospital · GBHospital of the University of Pennsylvania · US

Funding

Vector CoreP30DK047757 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI WILSON, JAMES M · 1993 to 2017
$18.0M
Clinical Pharmacoepidemiology Training ProgramT32GM075766 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI Sean Hennessy, Charles Edward Leonard · 2006 to 2026
$8.4M
Medical Research Council G0100266Medical Research Council MC_PC_12033NIDDK NIH HHS DK047757
6 · The paper itself

Abstract

Cystic fibrosis (CF) is one of the most common autosomal recessive lethal disorders affecting white populations of northern European ancestry. To date there is no cure for CF. Life-long treatments for CF are being developed and include gene therapy and the use of small-molecule drugs designed to target specific cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations. Irrespective of the type of molecular therapy for CF, which may include gene replacement, exon skipping, nonsense suppression, or molecular correctors, because all of these modulate gene expression there is an inherent risk of activation of T cells against the wild-type version of CFTR. Here we report the validation of the human interferon-γ enzyme-linked immunospot assay and its application for the analysis of CFTR-specific T cell responses in patients with CF and in non-CF subjects. We found non-CF subjects with low levels of self-reactive CFTR-specific T cells in the United States and several patients with CF with low to high levels of self-reactive CFTR-specific T cells in both the United States and the United Kingdom.

Indexed as

AutoimmunityAdolescentAdultAnimalsCystic FibrosisCystic Fibrosis Transmembrane Conductance RegulatorEnzyme-Linked Immunosorbent AssayFemaleGenetic TherapyHumansInterferon-gammaInterferon-gamma Release TestsMaleMiceMiddle AgedT-LymphocytesCFTR protein, humanCystic Fibrosis Transmembrane Conductance RegulatorInterferon-gamma

Identifiers

PMID23790242
PMCPMC4003469
OpenAlexW2056619127

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.