Safety, Tolerability, and Immunogenicity of a DNA Vaccine (pGX9501) Against SARS-CoV-2 in Healthy Volunteers: A Single-Center, Randomized, Double-Blind, Placebo-Controlled, and Dose-Ranging Phase I Trial.

Publication date: May 27, 2025

Background: pGX9501 is a prophylactic DNA vaccine encoding the spike protein of SARS-CoV-2 and can induce immune response in the human body so as to prevent COVID-19. With respect to non-clinical studies, pGX9501 has been demonstrated to induce both cellular and humoral immune responses in various animal models. It was found that the level of antibody titers following a two-dose regimen was higher than that following a single-dose regimen in nonhuman primate challenge model. Methods: In China, a phase I, randomized, double-blind, placebo-controlled clinical trial has been conducted in Huashan Hospital, Shanghai, China to evaluate the safety, tolerability, and immunogenicity of DNA vaccine pGX9501 administered intradermally (ID) followed by electroporation (EP) in 45 Chinese healthy volunteers aged 18 to 59 years old. Results: No adverse events of special interest (AESIs), death, or treatment-related SAEs occurred in this study. All the treatment-related (vaccine or EP) adverse events (TRAEs) were of grade 1 and 2 in severity. The solicited AEs were reported in thirty-two (32/36, 88. 9%) and nine (9/9, 100. 0%) subjects, respectively, in the DNA vaccine and placebo group. The frequency of solicited AEs did not increase with vaccine dose level and frequency. The DNA vaccine pGX9501 effectively enhanced both humoral and cellular immune responses in a dose-dependent manner, with increased antibody GMTs and peak seroconversion rates observed on day 42. The significant rise in IFN-γ levels confirmed the vaccine’s ability to induce cellular immune responses. Variations in the microbiome structure suggested a tangible impact of the gut microbiota on vaccine immunogenicity. Conclusions: The findings from this study confirm the immunogenicity and safety of the DNA vaccine pGX9501 and point to the potential role of the gut microbiota in vaccine immune responses. These insights provide practical references for the future design and development of DNA vaccines.

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Concepts Keywords
China acute respiratory disease
Death COVID-19
Models DNA vaccine
Vaccine pGX9501(INO-4800)
SARS-CoV-2

Semantics

Type Source Name
disease IDO protein
disease IDO immune response
disease MESH COVID-19
disease MESH death
disease MESH seroconversion
disease IDO role
disease MESH Infectious Disease
pathway REACTOME Infectious disease
drug DRUGBANK Coenzyme M
disease IDO cell
disease IDO infectivity
disease IDO process
disease IDO host
drug DRUGBANK Inosine
disease MESH Middle East respiratory syndrome
disease IDO site
drug DRUGBANK Methionine
disease IDO assay
disease MESH hepatitis
drug DRUGBANK Hepatitis B Vaccine (Recombinant)
disease MESH syphilis
disease IDO immunodeficiency
disease MESH HIV infection
pathway REACTOME HIV Infection
disease MESH hypersensitivity
disease IDO history
disease MESH mental illness
disease IDO humoral immune response
drug DRUGBANK Sodium Chloride
drug DRUGBANK Sodium Citrate
disease MESH contraindications
disease MESH abnormalities
disease IDO blood
drug DRUGBANK Etoperidone
drug DRUGBANK Immune Globulin Human
disease MESH viral infection
drug DRUGBANK Nitrogen
disease IDO reagent
drug DRUGBANK Dimethyl sulfoxide
disease IDO disposition
disease MESH erythema
drug DRUGBANK Pidolic Acid
pathway REACTOME Metabolism
drug DRUGBANK Amino acids
disease IDO production
drug DRUGBANK Pentaerythritol tetranitrate
disease MESH emergency
disease MESH injection site reactions
disease MESH cervical intraepithelial neoplasia
disease MESH cancer
drug DRUGBANK Guanosine
disease MESH malaria
pathway KEGG Malaria

Original Article

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