Evidence map›Paper›PMID 37296017›Full record

Trial reportVaccine2023

Immune response enhancement with GLS-5310 DNA primary vaccine against SARS-CoV-2 followed by administration of an mRNA vaccine heterologous boost.

Woo Joo Kim, Christine C Roberts, Joon Young Song, Jin Gu Yoon, Hye Seong, Hak-Jun Hyun, Hyojin Lee, Areum Gil, Yeeun Oh, Ji-Eun Park and 9 more

Open access · hybridAbstract readClinical Trial
In one paragraph

Trial report in Vaccine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. 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

19 authors at 2 institutions in 2 countries.

Woo Joo KimDivision of Infectious Diseases, Guro Hospital, Vaccine Innovation Center, Korea University, College of Medicine, Seoul, Republic of Korea.
Christine C RobertsGeneOne Life Science, Inc., Seoul, Republic of Korea.
Joon Young SongDivision of Infectious Diseases, Guro Hospital, Vaccine Innovation Center, Korea University, College of Medicine, Seoul, Republic of Korea.
Jin Gu YoonDivision of Infectious Diseases, Guro Hospital, Vaccine Innovation Center, Korea University, College of Medicine, Seoul, Republic of Korea.
Hye SeongDivision of Infectious Diseases, Guro Hospital, Vaccine Innovation Center, Korea University, College of Medicine, Seoul, Republic of Korea.
Hak-Jun HyunDivision of Infectious Diseases, Guro Hospital, Vaccine Innovation Center, Korea University, College of Medicine, Seoul, Republic of Korea.
Hyojin LeeGeneOne Life Science, Inc., Seoul, Republic of Korea.
Areum GilGeneOne Life Science, Inc., Seoul, Republic of Korea.
Yeeun OhGeneOne Life Science, Inc., Seoul, Republic of Korea.
Ji-Eun ParkGeneOne Life Science, Inc., Seoul, Republic of Korea.
Ji-Eun LeeGeneOne Life Science, Inc., Seoul, Republic of Korea.
Bohyun JeonGeneOne Life Science, Inc., Seoul, Republic of Korea.
Deborah KaneGeneOne Life Science, Inc., Seoul, Republic of Korea.
Susan SpruillApplied Statistics and Consulting, Spruce Pine, NC, USA.
Sagar B KudchodkarGeneOne Life Science, Inc., Seoul, Republic of Korea.
Kar MuthumaniGeneOne Life Science, Inc., Seoul, Republic of Korea.
Young K ParkGeneOne Life Science, Inc., Seoul, Republic of Korea.
Ijoo KwonGeneOne Life Science, Inc., Seoul, Republic of Korea.
Joel N MaslowGeneOne Life Science, Inc., Seoul, Republic of Korea; Department of Medicine, Morristown Medical Center, Morristown, NJ, USA. Electronic address: jmaslow@genels.us.
Korea University Medical Center · KRMorristown Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Heterologous boost regimens are being increasingly considered against SARS-CoV-2. We report results for the 32 of 45 participants in the Phase 1 CoV2-001 clinical trial (Kim et al., Int J Iinfect Dis 2023, 128:112-120) who elected to receive an EUA-approved SARS-CoV-2 mRNA vaccine 6 to 8 months following a two-dose primary vaccination with the GLS-5310 bi-cistronic DNA vaccine given intradermally and followed by application of suction using the GeneDerm device. Receipt of EUA-approved mRNA vaccines after GLS-5310 vaccination was well-tolerated, with no reported adverse events. Immune responses were enhanced such that binding antibody titers, neutralizing antibody titers, and T-cell responses increased 1,187-fold, 110-fold, and 2.9-fold, respectively. This paper is the first description of the immune responses following heterologous vaccination with a DNA primary series and mRNA boost.

Indexed as

COVID-19Vaccines, DNAAntibodies, NeutralizingAntibodies, ViralCOVID-19 VaccinesDNAHumansmRNA VaccinesSARS-CoV-2VaccinationAntibodies, NeutralizingAntibodies, ViralCOVID-19 VaccinesDNAGLS-5310 vaccinemRNA VaccinesVaccines, DNA

Identifiers

PMID37296017
PMCPMC10242151
OpenAlexW4379535998

What Socratic 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 Socratic graph.