Safety and Immunogenicity of an Andes Virus DNA Vaccine by Needle-Free Injection: a Randomized, Controlled Phase 1 Study.
Jun-23
Journal Article
Authors:
            
  
    Paulsen, G.C.; 
          
  
    Frenck, R.; 
          
  
    Tomashek, K.M.; 
          
  
    Alarcon, R.M.; 
          
  
    Hensel, E.; 
          
  
    Lowe, A.; 
          
  
    Brocato, R.L.; 
          
  
    Kwilas, S.A.; 
          
  
    Josleyn, M.D.; 
          
  
    Hooper, J.W.
  
Secondary:
            J Infect Dis
      
Volume:
229
Pagination:
30-38
Issue:
1
Journal:
            J Infect Dis
      
PMID:
37380156
URL:
            https://www.ncbi.nlm.nih.gov/pubmed/37380156
      
Keywords:
      
              Adult
              Humans
              *Orthohantavirus
              *Vaccines, DNA/adverse effects
              Antibodies, Neutralizing
              *Hantavirus Pulmonary Syndrome
              DNA
              Immunogenicity, Vaccine
              Double-Blind Method
              Antibodies, Viral
              Andes
              DNA vaccine
              hantavirus
              hantavirus pulmonary syndrome
              needle-free injection
          
  
Abstract:
            <p>BACKGROUND: Andes virus (ANDV), a rodent-borne hantavirus, causes hantavirus pulmonary syndrome (HPS). The safety and immunogenicity of a novel ANDV DNA vaccine was evaluated. METHODS: Phase 1, double-blind, dose-escalation trial randomly assigned 48 healthy adults to placebo or ANDV DNA vaccine delivered via needle-free jet injection. Cohorts 1 and 2 received 2 mg of DNA or placebo in a 3-dose (days 1, 29, 169) or 4-dose (days 1, 29, 57, 169) schedule, respectively. Cohorts 3 and 4 received 4 mg of DNA or placebo in the 3-dose and 4-dose schedule, respectively. Subjects were monitored for safety and neutralizing antibodies by pseudovirion neutralization assay (PsVNA50) and plaque reduction neutralization test (PRNT50). RESULTS: While 98% and 65% of subjects had at least 1 local or systemic solicited adverse event (AE), respectively, most AEs were mild or moderate; no related serious AEs were detected. Cohorts 2, 3, and 4 had higher seroconversion rates than cohort 1 and seropositivity of at least 80% by day 197, sustained through day 337. PsVNA50 geometric mean titers were highest for cohort 4 on and after day 197. CONCLUSIONS: This first-in-human candidate HPS vaccine trial demonstrated that an ANDV DNA vaccine was safe and induced a robust, durable immune response. Clinical Trials Registration. NCT03682107.</p>