Evidence map›Paper›PMID 36757308›Full record

ArticleCancer immunology research2023

Combination IFNβ and Membrane-Stable CD40L Maximize Tumor Dendritic Cell Activation and Lymph Node Trafficking to Elicit Systemic T-cell Immunity.

Hong Zheng, Xiaoqing Yu, Mohammed L Ibrahim, Dana Foresman, Mengyu Xie, Joseph O Johnson, Theresa A Boyle, Brian Ruffell, Bradford A Perez, Scott J Antonia and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer immunology research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
4.4field-weighted citation impact, top 6% 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

13 citing papers in PubMed, 14 citations in OpenAlex.

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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.

Hong ZhengDepartment of Immunology, Moffitt Cancer Center, Tampa, Florida.ORCID 0000-0002-2136-3279
Xiaoqing YuBiostatistics and Bioinformatics, Moffitt Cancer Center, Tampa, Florida.ORCID 0000-0003-4585-9372
Mohammed L IbrahimDepartment of Immunology, Moffitt Cancer Center, Tampa, Florida.ORCID 0000-0002-1686-0561
Dana ForesmanDepartment of Immunology, Moffitt Cancer Center, Tampa, Florida.ORCID 0000-0001-6362-3262
Mengyu XieDepartment of Immunology, Moffitt Cancer Center, Tampa, Florida.ORCID 0000-0002-4661-9891
Joseph O JohnsonAnalytical Microscopy, Moffitt Cancer Center, Tampa, Florida.ORCID 0000-0001-8574-6909
Theresa A BoylePathology, Moffitt Cancer Center, Tampa, Florida.ORCID 0000-0001-5950-3970
Brian RuffellDepartment of Immunology, Moffitt Cancer Center, Tampa, Florida.ORCID 0000-0002-3846-6872
Bradford A PerezRadiation Oncology, Moffitt Cancer Center, Tampa, Florida.ORCID 0000-0001-5725-195X
Scott J AntoniaDuke Cancer Institute, Duke University School of Medicine, Durham, North Carolina.ORCID 0000-0002-0029-9685
Neal ReadyDuke Cancer Institute, Duke University School of Medicine, Durham, North Carolina.ORCID 0000-0003-4414-9432
Andreas N SaltosThoracic Oncology, Moffitt Cancer Center, Tampa, Florida.ORCID 0000-0003-3622-026X
Mark J CantwellMemgen Inc., Houston, Texas.ORCID 0000-0002-7298-0787
Amer A BegDepartment of Immunology, Moffitt Cancer Center, Tampa, Florida.ORCID 0000-0003-3834-774X
Moffitt Cancer Center · USDuke University · USCairo University · EGNewGen Therapeutics (United States) · US

Funding

TRANSLATIONAL RESEARCHP30CA076292 · NCI · UNIVERSITY OF SOUTH FLORIDA · PI Christine O'Connell · 1998 to 2026
$93.5M
Tissue, Pathology and BioinformaticsP50CA168536 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI MULE, JAMES J. · 2013 to 2017
$8.5M
NCI NIH HHS P30 CA076292NCI NIH HHS P50 CA168536
6 · The paper itself

Abstract

Oncolytic virus therapies induce the direct killing of tumor cells and activation of conventional dendritic cells (cDC); however, cDC activation has not been optimized with current therapies. We evaluated the adenoviral delivery of engineered membrane-stable CD40L (MEM40) and IFNβ to locally activate cDCs in mouse tumor models. Combined tumor MEM40 and IFNβ expression induced the highest cDC activation coupled with increased lymph node migration, increased systemic antitumor CD8+ T-cell responses, and regression of established tumors in a cDC1-dependent manner. MEM40 + IFNβ combined with checkpoint inhibitors led to effective control of distant tumors and lung metastases. An oncolytic adenovirus (MEM-288) expressing MEM40 + IFNβ  in phase I clinical testing induced cancer cell loss concomitant with enhanced T-cell infiltration and increased systemic presence of tumor T-cell clonotypes in non-small cell lung cancer (NSCLC) patients. This approach to simultaneously target two major DC-activating pathways has the potential to significantly affect the solid tumor immunotherapy landscape.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsAnimalsCD40 LigandCD8-Positive T-LymphocytesCell Line, TumorDendritic CellsImmunotherapyMiceCD40 Ligand

Identifiers

PMID36757308
PMCPMC10165690
OpenAlexW4319656721

What OpenQuestion holds

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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.