Evidence map›Paper›PMID 39276533›Full record

ArticleNeoplasia (New York, N.Y.)2024

Oncolytic adenovirus MEM-288 encoding membrane-stable CD40L and IFNβ induces an anti-tumor immune response in high grade serous ovarian cancer.

Pamela N Peters, Regina S Whitaker, Felicia Lim, Shonagh Russell, Elizabeth A Bloom, Justin Pollara, Kyle C Strickland, Mark J Cantwell, Amer Beg, Andrew Berchuck and 2 more

Abstract read
In one paragraph

Article in Neoplasia (New York, N.Y.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
–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

11 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. Review
  9. Four decades of adenovirus gene transfer vectors: History and current use.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  10. Review
  11. 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

12 authors.

Pamela N PetersDuke University Department of Obstetrics and Gynecology. Electronic address: pamela.peters@duke.edu.
Regina S WhitakerDuke University Department of Obstetrics and Gynecology.
Felicia LimDuke University Department of Pharmacology and Cancer Biology.
Shonagh RussellDuke University Department of Pharmacology and Cancer Biology.
Elizabeth A BloomDuke University School of Medicine.
Justin PollaraDuke University Department of Surgery.
Kyle C StricklandDuke University Department of Pathology; Labcorp Oncology, Durham, NC, USA.
Mark J CantwellMemgen, Inc.
Amer BegMoffitt Cancer Center Department of Immunology.
Andrew BerchuckDuke University Department of Obstetrics and Gynecology.
Scott AntoniaLabcorp Oncology, Durham, NC, USA.
Rebecca A PrevisDuke University Department of Obstetrics and Gynecology; Labcorp Oncology, Durham, NC, USA.

Funding

Duke Women's Reproductive Health Research ScholarsK12HD103083 · NICHD · DUKE UNIVERSITY · PI Cindy Amundsen · 2020 to 2026
$2.2M
Duke-UNC Chapel Hill Immunotherapy Training GrantT32CA211056 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI CHAO, NELSON J., SERODY, JONATHAN S. · 2017 to 2021
$2.2M
NCI NIH HHS T32 CA211056NICHD NIH HHS K12 HD103083
6 · The paper itself

Abstract

Single agent immune checkpoint inhibitors have been ineffective for patients with advanced stage and recurrent high grade serous ovarian cancer (HGSOC). Using pre-clinical models of HGSOC, we evaluated the anti-tumor and immune stimulatory effects of an oncolytic adenovirus, MEM-288. This conditionally replicative virus encodes a modified membrane stable CD40L and IFNβ. We demonstrated this virus successfully infects HGSOC cell lines and primary human ascites samples in vitro. We evaluated the anti-tumor and immunostimulatory activity in vivo in immune competent mouse models. Intraperitoneal delivery of MEM-288 decreased ascites and solid tumor burden compared to controls, and treatment generated a systemic anti-tumor immune response. The tumor microenvironment had a higher proportion of anti-tumor macrophages and decreased markers of angiogenesis. MEM-288 is a promising immunotherapy agent in HGSOC, with further pre-clinical studies required to understand the mechanism of action in the peritoneal microenvironment and clinical activity in combination with other therapies.

Indexed as

AdenoviridaeCD40 LigandCystadenocarcinoma, SerousInterferon-betaOncolytic VirotherapyOncolytic VirusesOvarian NeoplasmsTumor MicroenvironmentXenograft Model Antitumor AssaysAnimalsCell Line, TumorDisease Models, AnimalFemaleGenetic VectorsHumansImmunotherapyCD40 LigandInterferon-betaAscitesELISAELISPOTImmunotherapyIntraperitonealMicroenvironmentOncolytic virusOvarian cancer

Identifiers

PMID39276533
PMCPMC11417341

What OpenQuestion holds

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LicenceCC BY
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.