Evidence map›Paper›PMID 35492876›Full record

ArticleCell reports. Medicine2022

Promoting antigen escape from dendritic cell endosomes potentiates anti-tumoral immunity.

Jean-Pierre Bikorimana, Natasha Salame, Simon Beaudoin, Mohammad Balood, Théo Crosson, Jamilah Abusarah, Sebastien Talbot, Raimar Löbenberg, Sebastien Plouffe, Moutih Rafei

Open access · goldAbstract read
In one paragraph

Article in Cell reports. Medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

17 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
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  11. Local delivery of accutoxJournal of translational medicine · 2024
    Article
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  15. 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

10 authors at 2 institutions in 1 country.

Jean-Pierre BikorimanaDepartment of Microbiology, Infectiology and Immunology, Université de Montréal, Montréal, QC, Canada.
Natasha SalameDepartment of Biomedical Sciences, Université de Montréal, Montréal, QC, Canada.
Simon BeaudoinResearch and Development Branch, Defence Therapeutics Inc., Vancouver, BC, Canada.
Mohammad BaloodDepartment of Pharmacology and Physiology, Université de Montréal, Montréal, QC, Canada.
Théo CrossonDepartment of Pharmacology and Physiology, Université de Montréal, Montréal, QC, Canada.
Jamilah AbusarahDepartment of Pharmacology and Physiology, Université de Montréal, Montréal, QC, Canada.
Sebastien TalbotDepartment of Pharmacology and Physiology, Université de Montréal, Montréal, QC, Canada.
Raimar LöbenbergDepartment of Pharmacy and Pharmaceutical Sciences, University of Alberta, Edmonton, AB, Canada.
Sebastien PlouffeResearch and Development Branch, Defence Therapeutics Inc., Vancouver, BC, Canada.
Moutih RafeiDepartment of Microbiology, Infectiology and Immunology, Université de Montréal, Montréal, QC, Canada.
Université de Montréal · CAUniversity of Alberta · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The cross-presenting capacity of dendritic cells (DCs) can be limited by non-specific degradation during endosome maturation. To bypass this limitation, we present in this study a new Accum-based formulation designed to promote endosome-to-cytosol escape. Treatment of primary DCs with Accum linked to the xenoantigen ovalbumin (OVA) triggers endosomal damages and enhances protein processing. Despite multiple challenges using ascending doses of tumor cells, DC prophylactic vaccination results in complete protection due to increased levels of effector CD4 and CD8 T cells as well as high production of pro-inflammatory mediators. When combined with anti-PD-1, therapeutic vaccination using both syngeneic and allogeneic Accum-OVA-pulsed DCs triggers potent anti-tumoral responses. The net outcome culminates in increased CD11c, CD8, and NK infiltration along with a high CD8/Treg ratio. These highly favorable therapeutic effects highlight the promising potential of Accum as a distinct and potent technology platform suitable for the design of next generation cell cancer vaccines.

Indexed as

Cancer VaccinesDendritic CellsAntigenic Drift and ShiftCD8-Positive T-LymphocytesEndosomesOvalbuminCancer VaccinesOvalbuminAccumantigen cross-presentationanti-tumoral immunitydendritic cellsendosomesimmune checkpoint inhibitorstumor-infiltrating lymphocytes

Identifiers

PMID35492876
PMCPMC9040180
OpenAlexW4225319991

What OpenQuestion holds

Textmetadata
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.