Evidence map›Paper›PMID 19073718›Full record

ArticleJournal of virology2009

Effect of preexisting immunity on oncolytic adenovirus vector INGN 007 antitumor efficacy in immunocompetent and immunosuppressed Syrian hamsters.

Debanjan Dhar, Jacqueline F Spencer, Karoly Toth, William S M Wold

Abstract read
In one paragraph

Article in Journal of virology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing 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

46 citing papers in PubMed.

  1. Trial
  2. Article
  3. Cancer viroimmunotherapy platforms based on varicella-zoster virus and cytomegalovirus.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
    Review
  4. Review
  5. Review
  6. Review
  7. Therapy with oncolytic viruses: progress and challenges.Nature reviews. Clinical oncology · 2023
    Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Oncolytic Virotherapy: A Contest between Apples and Oranges.Molecular therapy : the journal of the American Society of Gene Therapy · 2017
    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

4 authors.

Debanjan DharDepartment of Molecular Microbiology and Immunology, Saint Louis University School of Medicine, 1100 S. Grand Blvd., Saint Louis, Missouri 63104, USA.
Jacqueline F Spencer
Karoly Toth
William S M Wold

Funding

Hamster Model for Oncolytic Adenovirus VectorsR01CA118022 · NCI · SAINT LOUIS UNIVERSITY · PI WOLD, WILLIAM SM · 2006 to 2010
$1.3M
Adenovirus Replication-Competent Anti-Cancer VectorR42CA081829 · NCI · VIRRX, INC · PI WOLD, WILLIAM SM · 2002 to 2003
$711k
Animal Model for Adenovirus Oncolytic VectorsR41CA108335 · NCI · VIRRX, INC · PI WOLD, WILLIAM SM · 2004 to 2004
$182k
ADENOVIRUS REPLICATION COMPETENT ANTICANCER VECTORR41CA081829 · NCI · VIRRX, INC · PI WOLD, WILLIAM SM · 1999 to 1999
–
NCI NIH HHS CA108335NCI NIH HHS CA118022NCI NIH HHS CA81829NCI NIH HHS R01 CA118022NCI NIH HHS R41 CA081829NCI NIH HHS R41 CA108335NCI NIH HHS R42 CA081829
6 · The paper itself

Abstract

Immune responses against adenovirus (Ad) vectors pose a possible concern for the outcome of treatment efficacy. To address the role of preexisting immunity in oncolytic Ad vector antitumor efficacy following intratumoral injection of vector as well as tumor-to-tissue spread of the vector, we employed the Syrian hamster model. These animals are immunocompetent, and their tumors and tissues are permissive for replication of Ad type 5 (Ad5). We used the adenovirus death protein-overexpressing Ad5-based vector INGN 007. Subcutaneous tumors were established in groups of hamsters that were or were not immunized with Ad5. Half of the hamsters in these groups were immunosuppressed with cyclophosphamide. For all groups, tumors injected with INGN 007 grew significantly more slowly than those injected with buffer. Under immunocompetent conditions, there was no significant effect of preexisting immunity on vector antitumor efficacy. Soon after the tumors in naïve animals were injected with vector, the hamsters developed neutralizing antibody (NAb) and the difference in NAb titers between the naïve and immunized groups diminished. Under immunosuppressed conditions, preexisting NAb did significantly reduce vector efficacy. Thus, NAb do reduce vector efficacy to some extent, but immunosuppression is required to observe the effect. Regarding vector toxicity, there was spillover of vector from the tumor to the liver and lungs in naïve immunocompetent hamsters, and this was nearly eliminated in the immunized hamsters. Thus, preexisting immunity to Ad5 does not affect INGN 007 antitumor efficacy following intratumoral injection, but immunity prevents vector spillover from the tumor to the liver and lungs.

Indexed as

Oncolytic VirotherapyAdenoviridaeAnimalsAntibodies, ViralCell Line, TumorCricetinaeCyclophosphamideGenetic VectorsHumansImmunocompetenceImmunosuppression TherapyLiverLungMesocricetusModels, AnimalNeoplasms, ExperimentalAntibodies, ViralCyclophosphamide

Identifiers

PMID19073718
PMCPMC2643738

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.