Evidence map›Paper›PMID 38302823›Full record

ArticleAdvanced materials (Deerfield Beach, Fla.)2024

Extracellular Matrix Scaffold-Assisted Tumor Vaccines Induce Tumor Regression and Long-Term Immune Memory.

Sanjay Pal, Rohan Chaudhari, Iris Baurceanu, Brenna J Hill, Bethany A Nagy, Matthew T Wolf

Open access · greenAbstract read
In one paragraph

Article in Advanced materials (Deerfield Beach, Fla.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
6.3field-weighted citation impact, top 3% 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

12 citing papers in PubMed, 26 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

6 authors at 3 institutions in 1 country.

Sanjay PalCancer Biomaterials Engineering Section, Cancer Innovation Laboratory, Center for Cancer Research, National Cancer Institute, Frederick, MD, 21702, USA.ORCID https://orcid.org/0000-0003-3959-6844
Rohan ChaudhariCancer Biomaterials Engineering Section, Cancer Innovation Laboratory, Center for Cancer Research, National Cancer Institute, Frederick, MD, 21702, USA.ORCID https://orcid.org/0000-0003-2473-0895
Iris BaurceanuCancer Biomaterials Engineering Section, Cancer Innovation Laboratory, Center for Cancer Research, National Cancer Institute, Frederick, MD, 21702, USA.ORCID https://orcid.org/0009-0008-3592-7670
Brenna J HillAIDS and Cancer Virus Program, Frederick National Laboratory for Cancer Research, Frederick, MD, 21702, USA.ORCID https://orcid.org/0000-0002-7068-6672
Bethany A NagyLaboratory Animal Sciences Program (LASP), National Cancer Institute, Frederick, MD, 21702, USA.ORCID https://orcid.org/0000-0001-7454-9344
Matthew T WolfCancer Biomaterials Engineering Section, Cancer Innovation Laboratory, Center for Cancer Research, National Cancer Institute, Frederick, MD, 21702, USA.ORCID https://orcid.org/0000-0002-0328-2475
National Cancer Institute · USFrederick National Laboratory for Cancer Research · USOregon Health & Science University · US

Funding

Cancer Biomaterials EngineeringZIABC012021 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI WOLF, MATTHEW · 2020 to 2025
$6.7M
CCR NIH HHSIntramural NIH HHS Z99 CA999999Intramural NIH HHS ZIA BC012021NCI NIH HHS
6 · The paper itself

Abstract

Injectable scaffold delivery is a strategy to enhance the efficacy of cancer vaccine immunotherapy. The choice of scaffold biomaterial is crucial, impacting both vaccine release kinetics and immune stimulation via the host response. Extracellular matrix (ECM) scaffolds prepared from decellularized tissues facilitate a pro-healing inflammatory response that promotes local cancer immune surveillance. Here, an ECM scaffold-assisted therapeutic cancer vaccine that maintains an immune microenvironment consistent with tissue reconstruction is engineered. Several immune-stimulating adjuvants are screened to develop a cancer vaccine formulated with decellularized small intestinal submucosa (SIS) ECM scaffold co-delivery. It is found that the STING pathway agonist cyclic di-AMP most effectively induces cytotoxic immunity in an ECM scaffold vaccine, without compromising key interleukin 4 (IL-4) mediated immune pathways associated with healing. ECM scaffold delivery enhances therapeutic vaccine efficacy, curing 50-75% of established E.G-7OVA lymphoma tumors in mice, while none are cured with soluble vaccine. SIS-ECM scaffold-assisted vaccination prolonged antigen exposure is dependent on CD8

Indexed as

Cancer VaccinesNeoplasmsAnimalsDinucleoside PhosphatesExtracellular MatrixImmunologic MemoryInterleukin-4MiceTissue ScaffoldsTumor MicroenvironmentCancer Vaccinescyclic diadenosine phosphateDinucleoside PhosphatesInterleukin-4biomaterialscancer immunotherapycancer vaccinedecellularized extracellular matriximmunoengineering

Identifiers

PMID38302823
PMCPMC11009079
OpenAlexW4391481327

What OpenQuestion holds

Textmetadata
LicenceTDM
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.