Evidence map›Paper›PMID 35028603›Full record

ArticleCell reports. Medicine2021

Engineering immunoproteasome-expressing mesenchymal stromal cells: A potent cellular vaccine for lymphoma and melanoma in mice.

Jamilah Abusarah, Fatemeh Khodayarian, Nehme El-Hachem, Natasha Salame, Martin Olivier, Mohammad Balood, Katiane Roversi, Sebastien Talbot, Jean-Pierre Bikorimana, Jingkui Chen and 9 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports. Medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

22 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
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  9. Local delivery of accutoxJournal of translational medicine · 2024
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  17. TheiScience · 2022
    Article
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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

19 authors at 5 institutions in 1 country.

Jamilah AbusarahDepartment of Microbiology and Immunology, McGill University, Montreal, QC, Canada.
Fatemeh KhodayarianDepartment of Pharmacology and Physiology, Université de Montréal, Montreal, QC, Canada.
Nehme El-HachemDepartment of Pharmacology and Physiology, Université de Montréal, Montreal, QC, Canada.
Natasha SalameDepartment of Biomedical Sciences, Université de Montréal, Montreal, QC, Canada.
Martin OlivierDepartment of Microbiology and Immunology, McGill University, Montreal, QC, Canada.
Mohammad BaloodDepartment of Pharmacology and Physiology, Université de Montréal, Montreal, QC, Canada.
Katiane RoversiDepartment of Pharmacology and Physiology, Université de Montréal, Montreal, QC, Canada.
Sebastien TalbotDepartment of Pharmacology and Physiology, Université de Montréal, Montreal, QC, Canada.
Jean-Pierre BikorimanaDepartment of Microbiology, Infectious Diseases and Immunology, Université de Montréal, Montreal, QC, Canada.
Jingkui ChenResearch Laboratory in Applied Metabolic Engineering, Department of Chemical Engineering, Polytechnique Montréal, Montreal, QC, Canada.
Mario JolicoeurResearch Laboratory in Applied Metabolic Engineering, Department of Chemical Engineering, Polytechnique Montréal, Montreal, QC, Canada.
Louis-Eric TrudeauDepartment of Pharmacology and Physiology, Université de Montréal, Montreal, QC, Canada.
Samaneh KamyabiazarDepartment of Chemistry, Université du Québec à Montréal, Montreal, QC, Canada.
Borhane AnnabiDepartment of Chemistry, Université du Québec à Montréal, Montreal, QC, Canada.
Francis RobertDepartment of Biochemistry, McGill University, Montreal, QC, Canada.
Jerry PelletierDepartment of Biochemistry, McGill University, Montreal, QC, Canada.
Abed-El-Hakim El-KadiryDepartment of Pharmacology and Physiology, Université de Montréal, Montreal, QC, Canada.
Riam ShammaaDepartment of Family and Community Medicine, University of Toronto, Toronto, ON, Canada.
Moutih RafeiDepartment of Microbiology and Immunology, McGill University, Montreal, QC, Canada.
Université de Montréal · CAMcGill University · CAPolytechnique Montréal · CAUniversité du Québec à Montréal · CAUniversity of Toronto · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dendritic cells (DCs) excel at cross-presenting antigens, but their effectiveness as cancer vaccine is limited. Here, we describe a vaccination approach using mesenchymal stromal cells (MSCs) engineered to express the immunoproteasome complex (MSC-IPr). Such modification instills efficient antigen cross-presentation abilities associated with enhanced major histocompatibility complex class I and CD80 expression,

Indexed as

Protein EngineeringAnimalsAntigen PresentationAntigen-Presenting CellsCancer VaccinesCellular ReprogrammingDendritic CellsFemaleImmune Checkpoint InhibitorsImmunityLymphomaMelanoma, ExperimentalMesenchymal Stem CellsMiceMice, Inbred C57BLOxidative PhosphorylationCancer VaccinesImmune Checkpoint InhibitorsProteasome Endopeptidase Complexcancer vaccineimmune-checkpoint blockersimmunopeptidomeimmunoproteasomemesenchymal stromal cellsmetabolomicsSILACstranscriptomicsuniversal vaccine

Identifiers

PMID35028603
PMCPMC8714858
OpenAlexW4200258848

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.