Evidence map›Paper›PMID 38339765›Full record

ArticleJournal of extracellular vesicles2024

Bioengineered small extracellular vesicles deliver multiple SARS-CoV-2 antigenic fragments and drive a broad immunological response.

Hannah K Jackson, Heather M Long, Juan Carlos Yam-Puc, Roberta Palmulli, Tracey A Haigh, Pehuén Pereyra Gerber, Jin S Lee, Nicholas J Matheson, Lesley Young, John Trowsdale and 4 more

Open access · goldAbstract read
In one paragraph

Article in Journal of extracellular vesicles, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
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 3 countries.

Hannah K JacksonDepartment of Pathology, University of Cambridge, Cambridge, UK.ORCID 0000-0002-4090-0885
Heather M LongInstitute of Immunology and Immunotherapy, University of Birmingham, Birmingham, UK.
Juan Carlos Yam-PucMRC Toxicology Unit, University of Cambridge, Cambridge, UK.
Roberta PalmulliDepartment of Pathology, University of Cambridge, Cambridge, UK.ORCID 0000-0003-2271-3186
Tracey A HaighInstitute of Immunology and Immunotherapy, University of Birmingham, Birmingham, UK.
Pehuén Pereyra GerberCambridge Institute of Therapeutic Immunology and Infectious Disease (CITIID), University of Cambridge, Cambridge, UK.
Jin S LeeDepartment of Pathology, University of Cambridge, Cambridge, UK.
Nicholas J MathesonCambridge Institute of Therapeutic Immunology and Infectious Disease (CITIID), University of Cambridge, Cambridge, UK.ORCID 0000-0002-3318-1851
Lesley YoungExosis, Inc. Palm Beach, Palm Beach, Florida, USA.
John TrowsdaleExosis, Inc. Palm Beach, Palm Beach, Florida, USA.
Mathew LoExosis, Inc. Palm Beach, Palm Beach, Florida, USA.
Graham S TaylorInstitute of Immunology and Immunotherapy, University of Birmingham, Birmingham, UK.
James E ThaventhiranMRC Toxicology Unit, University of Cambridge, Cambridge, UK.
James R EdgarDepartment of Pathology, University of Cambridge, Cambridge, UK.ORCID 0000-0001-7903-8199
University of Cambridge · GBPalm Beach Neurology · USUniversity of Birmingham · GBNHS Blood and Transplant · GB

Funding

Blood Cancer UK 20009Medical Research Council MC_UU_00025/12Medical Research Council MR/T032413/1MRF MRF-057-0002-RG-THAV-C0798MRF_ MRF-057-0002-RG-THAV-C0798Wellcome TrustWellcome Trust 204845/Z/16/ZWellcome Trust 216370/Z/19/Z
6 · The paper itself

Abstract

The COVID-19 pandemic highlighted the clear risk that zoonotic viruses pose to global health and economies. The scientific community responded by developing several efficacious vaccines which were expedited by the global need for vaccines. The emergence of SARS-CoV-2 breakthrough infections highlights the need for additional vaccine modalities to provide stronger, long-lived protective immunity. Here we report the design and preclinical testing of small extracellular vesicles (sEVs) as a multi-subunit vaccine. Cell lines were engineered to produce sEVs containing either the SARS-CoV-2 Spike receptor-binding domain, or an antigenic region from SARS-CoV-2 Nucleocapsid, or both in combination, and we tested their ability to evoke immune responses in vitro and in vivo. B cells incubated with bioengineered sEVs were potent activators of antigen-specific T cell clones. Mice immunised with sEVs containing both sRBD and Nucleocapsid antigens generated sRBD-specific IgGs, nucleocapsid-specific IgGs, which neutralised SARS-CoV-2 infection. sEV-based vaccines allow multiple antigens to be delivered simultaneously resulting in potent, broad immunity, and provide a quick, cheap, and reliable method to test vaccine candidates.

Indexed as

COVID-19Extracellular VesiclesVaccinesAnimalsHumansMicePandemicsSARS-CoV-2Vaccinesantigenextracellular vesiclesimmune presentationSARS-CoV-2vaccine

Identifiers

PMID38339765
PMCPMC10858312
OpenAlexW4391718342

What Socratic 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 Socratic graph.