Evidence map›Paper›PMID 34262675›Full record

ArticleJournal of extracellular vesicles2021

Synthetic bacterial vesicles combined with tumour extracellular vesicles as cancer immunotherapy.

Kyong-Su Park, Kristina Svennerholm, Rossella Crescitelli, Cecilia Lässer, Inta Gribonika, Jan Lötvall

Open access · goldAbstract read
In one paragraph

Article in Journal of extracellular vesicles, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed, 1 pooled it
7.1field-weighted citation impact, top 2% 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

80 citing papers in PubMed, 1 synthesis or guideline pooled it, 141 citations in OpenAlex.

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20 more citing papers are in PubMed but not listed here.

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 2 institutions in 2 countries.

Kyong-Su ParkKrefting Research Centre Institute of Medicine University of Gothenburg Gothenburg Sweden.
Kristina SvennerholmDepartment of Anesthesiology and Intensive Care Medicine Institute of Clinical Science Sahlgrenska Academy University of Gothenburg Gothenburg Sweden.
Rossella CrescitelliKrefting Research Centre Institute of Medicine University of Gothenburg Gothenburg Sweden.
Cecilia LässerKrefting Research Centre Institute of Medicine University of Gothenburg Gothenburg Sweden.
Inta GribonikaDepartment of Microbiology and Immunology Institute of Biomedicine University of Gothenburg Gothenburg Sweden.
Jan LötvallKrefting Research Centre Institute of Medicine University of Gothenburg Gothenburg Sweden.
University of Gothenburg · SEInstitute for Biomedicine · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bacterial outer membrane vesicles (OMV) have gained attention as a promising new cancer vaccine platform for efficiently provoking immune responses. However, OMV induce severe toxicity by activating the innate immune system. In this study, we applied a simple isolation approach to produce artificial OMV that we have named Synthetic Bacterial Vesicles (SyBV) that do not induce a severe toxic response. We also explored the potential of SyBV as an immunotherapy combined with tumour extracellular vesicles to induce anti-tumour immunity. Bacterial SyBV were produced with high yield by a protocol including lysozyme and high pH treatment, resulting in pure vesicles with very few cytosolic components and no RNA or DNA. These SyBV did not cause systemic pro-inflammatory cytokine responses in mice compared to naturally released OMV. However, SyBV and OMV were similarly effective in activation of mouse bone marrow-derived dendritic cells. Co-immunization with SyBV and melanoma extracellular vesicles elicited tumour regression in melanoma-bearing mice through Th-1 type T cell immunity and balanced antibody production. Also, the immunotherapeutic effect of SyBV was synergistically enhanced by anti-PD-1 inhibitor. Moreover, SyBV displayed significantly greater adjuvant activity than other classical adjuvants. Taken together, these results demonstrate a safe and efficient strategy for eliciting specific anti-tumour responses using immunotherapeutic bacterial SyBV.

Indexed as

ImmunotherapyAdjuvants, ImmunologicAnimalsArtificial CellsBacterial Outer MembraneCell Line, TumorCytokinesDendritic CellsEscherichia coliExtracellular VesiclesHumansImmune Checkpoint InhibitorsImmunizationMelanoma, ExperimentalMiceMice, Inbred C57BLAdjuvants, ImmunologicCytokinesImmune Checkpoint Inhibitorscancer immunotherapysynthetic bacterial vesiclestumour tissue extracellular vesicles

Identifiers

PMID34262675
PMCPMC8254025
OpenAlexW3178953948

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.