Evidence map›Paper›PMID 30770173›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2019

Self-Amplifying RNA Vaccines for Venezuelan Equine Encephalitis Virus Induce Robust Protective Immunogenicity in Mice.

Marcelo M Samsa, Lesley C Dupuy, Clayton W Beard, Carolyn M Six, Connie S Schmaljohn, Peter W Mason, Andrew J Geall, Jeffrey B Ulmer, Dong Yu

Open access · bronzeAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
7.1field-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

40 citing papers in PubMed, 60 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Research progress of mosquito-borne virus mRNA vaccines.Molecular therapy. Methods & clinical development · 2025
    Review
  8. Review
  9. Can self-amplifying RNA vaccines and viruses exchange genetic material?Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. Review
  16. Review
  17. Review
  18. Nanotechnology-based mRNA vaccines.Nature reviews. Methods primers · 2023
    Article
  19. Self-Amplifying RNA Approach for Protein Replacement Therapy.International journal of molecular sciences · 2022
    Review
  20. The Delivery of mRNA Vaccines for Therapeutics.Life (Basel, Switzerland) · 2022
    Review
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

9 authors at 3 institutions in 1 country.

Marcelo M SamsaGSK, Rockville, MD 20850, USA. Electronic address: marcelo.m.samsa@gsk.com.
Lesley C DupuyUnited States Army Medical Research Institute of Infectious Diseases, Fort Detrick, MD 21702, USA.
Clayton W BeardGSK, Rockville, MD 20850, USA.
Carolyn M SixUnited States Army Medical Research Institute of Infectious Diseases, Fort Detrick, MD 21702, USA.
Connie S SchmaljohnUnited States Army Medical Research Institute of Infectious Diseases, Fort Detrick, MD 21702, USA.
Peter W MasonNovartis Vaccines & Diagnostics, Cambridge, MA 02139, USA.
Andrew J GeallGSK, Rockville, MD 20850, USA.
Jeffrey B UlmerGSK, Rockville, MD 20850, USA.
Dong YuGSK, Rockville, MD 20850, USA. Electronic address: dong.x.yu@gsk.com.
GlaxoSmithKline (United States) · USUnited States Army Medical Research Institute of Infectious Diseases · USNovartis (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Venezuelan equine encephalitis virus (VEEV) is a known biological defense threat. A live-attenuated investigational vaccine, TC-83, is available, but it has a high non-response rate and can also cause severe reactogenicity. We generated two novel VEE vaccine candidates using self-amplifying mRNA (SAM). LAV-CNE is a live-attenuated VEE SAM vaccine formulated with synthetic cationic nanoemulsion (CNE) and carrying the RNA genome of TC-83. IAV-CNE is an irreversibly-attenuated VEE SAM vaccine formulated with CNE, delivering a TC-83 genome lacking the capsid gene. LAV-CNE launches a TC-83 infection cycle in vaccinated subjects but eliminates the need for live-attenuated vaccine production and potentially reduces manufacturing time and complexity. IAV-CNE produces a single cycle of RNA amplification and antigen expression without generating infectious viruses in subjects, thereby creating a potentially safer alternative to live-attenuated vaccine. Here, we demonstrated that mice vaccinated with LAV-CNE elicited immune responses similar to those of TC-83, providing 100% protection against aerosol VEEV challenge. IAV-CNE was also immunogenic, resulting in significant protection against VEEV challenge. These studies demonstrate the proof of concept for using the SAM platform to streamline the development of effective attenuated vaccines against VEEV and closely related alphavirus pathogens such as western and eastern equine encephalitis and Chikungunya viruses.

Indexed as

Gene AmplificationImmunogenicity, VaccineA549 CellsAnimalsAntibodies, NeutralizingAntibodies, ViralDisease Models, AnimalEmulsionsEncephalitis Virus, Venezuelan EquineEncephalomyelitis, Venezuelan EquineFemaleHumansMiceMice, Inbred BALB CRNA, MessengerTransfectionAntibodies, NeutralizingAntibodies, ViralEmulsionsRNA, MessengerVaccines, AttenuatedViral VaccinesCNERNA vaccineSAMself-amplifying RNAVEEV vaccine

Identifiers

PMID30770173
PMCPMC6453513
OpenAlexW2910686626

What OpenQuestion holds

Textmetadata
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.