Evidence map›Paper›PMID 10906225›Full record

ArticleJournal of virology2000

Immune response to recombinant adenovirus in humans: capsid components from viral input are targets for vector-specific cytotoxic T lymphocytes.

V Molinier-Frenkel, H Gahery-Segard, M Mehtali, C Le Boulaire, S Ribault, P Boulanger, T Tursz, J G Guillet, F Farace

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
5.1field-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

47 citing papers in PubMed, 115 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Improving Molecular Therapy in the Kidney.Molecular diagnosis & therapy · 2020
    Review
  8. Article
  9. Development of Novel Adenoviral Vectors to Overcome Challenges Observed With HAdV-5-based Constructs.Molecular therapy : the journal of the American Society of Gene Therapy · 2016
    Review
  10. Article
  11. New insights into IL-12-mediated tumor suppression.Cell death and differentiation · 2015
    Review
  12. Article
  13. Cellular immune therapy for viral infections in transplant patients.The Indian journal of medical research · 2013
    Review
  14. Adenoviral Vectors for Hemophilia Gene Therapy.Journal of genetic syndromes & gene therapy · 2013
    Article
  15. Article
  16. Helper-Dependent Adenoviral Vectors.Journal of genetic syndromes & gene therapy · 2011
    Article
  17. Article
  18. Article
  19. Article
  20. Absence of systemic immune response to adenovectors after intraocular administration to children with retinoblastoma.Molecular therapy : the journal of the American Society of Gene Therapy · 2010
    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

9 authors at 5 institutions in 1 country.

V Molinier-FrenkelDépartements de Biologie Clinique ou de Médecine, Institut Gustave Roussy, 94805 Villejuif, France.
H Gahery-Segard
M Mehtali
C Le Boulaire
S Ribault
P Boulanger
T Tursz
J G Guillet
F Farace
Institut Gustave Roussy · FRTransgene (France) · FRHôpital Cochin · FRInstitut Cochin · FRVirologie et Pathologies Humaines · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We previously demonstrated that a single injection of 10(9) PFU of recombinant adenovirus into patients induces strong vector-specific immune responses (H. Gahéry-Ségard, V. Molinier-Frenkel, C. Le Boulaire, P. Saulnier, P. Opolon, R. Lengagne, E. Gautier, A. Le Cesne, L. Zitvogel, A. Venet, C. Schatz, M. Courtney, T. Le Chevalier, T. Tursz, J.-G. Guillet, and F. Farace, J. Clin. Investig. 100:2218-2226, 1997). In the present study we analyzed the mechanism of vector recognition by cytotoxic T lymphocytes (CTL). CD8(+) CTL lines were derived from two patients and maintained in long-term cultures. Target cell infections with E1-deleted and E1-plus E2-deleted adenoviruses, as well as transcription-blocking experiments with actinomycin D, revealed that host T-cell recognition did not require viral gene transcription. Target cells treated with brefeldin A were not lysed, indicating that viral input protein-derived peptides are associated with HLA class I molecules. Using recombinant capsid component-loaded targets, we observed that the three major proteins could be recognized. These results raise the question of the use of multideleted adenoviruses for gene therapy in the quest to diminish antivector CTL responses.

Indexed as

Recombination, GeneticAdenoviridaeCapsidCell LineCytotoxicity, ImmunologicGenetic VectorsHistocompatibility Antigens Class IHumansT-Lymphocytes, CytotoxicHistocompatibility Antigens Class I

Identifiers

PMID10906225
PMCPMC112292
OpenAlexW2018628417

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.