High Frequency of Chronic Urticaria Following an Investigational HIV-1 BG505 MD39.3 Trimer mRNA Vaccine in a Phase 1, Randomized, Open-Label Clinical Trial (HVTN 302)

医学 试验药物 随机对照试验 临床试验 人类免疫缺陷病毒(HIV) 药理学 内科学 免疫学
作者
Sharon A. Riddler,Zoe Moodie,Jesse L. Clark,Catherine Yen,Mary Allen,Briana D. Furch,Huiyin Lu,Shannon Grant,Kajari Mondal,Maija Anderson,Janine Maenza,Maria P. Lemos,Amanda S. Woodward Davis,Stephen R. Walsh,Magdalena E. Sobieszczyk,Ian Frank,Paul A. Goepfert,Kathryn E. Stephenson,Lindsey R. Baden,Hong‐Van Tieu
出处
期刊:Annals of Internal Medicine [American College of Physicians]
被引量:2
标识
DOI:10.7326/annals-24-02701
摘要

The mRNA platform is under investigation for many vaccines, including HIV-1 vaccines. To evaluate the safety and tolerability of 3 investigational HIV-1 trimer mRNA vaccines. Safety analysis of mRNA vaccination in a phase 1, randomized, open-label trial. (ClinicalTrials.gov: NCT05217641). Ten research sites in the United States. 108 volunteers aged 18 to 55 years without HIV-1. Investigational HIV-1 BG505 MD39.3 trimer mRNA vaccines (gp140 soluble trimer, gp151 membrane-bound trimer, and gp151 CD4KO membrane-bound trimer) at doses of 100 and 250 mcg at 0, 2, and 6 months. Solicited and unsolicited adverse reactions and events reported during the 12 months after the first vaccination. Participants (n = 108) were randomly assigned to 6 vaccine groups. Mild to moderate local and systemic solicited events were common. Eighty participants reported 190 unsolicited adverse events (AEs); 30 were considered to be related to a study product. Most (73%) related AEs were mild, and the rest were moderate. Among related AEs, urticaria was reported by 7 of 108 participants (7% [95% CI, 3% to 13%]), 4 of whom had unresolved, intermittent urticaria at 12 months. In post hoc analyses, demographic characteristics, history of allergy or medication use, and COVID-19 were not associated with urticaria. In a comparison of participants with versus without urticaria, 100% (7 of 7; CI, 65% to 100%) versus 37% (37 of 101; CI, 28% to 46%) reported previous Moderna COVID-19 vaccination, 29% (2 of 7; CI, 8% to 64%) versus 76% (77 of 101; CI, 67% to 84%) reported previous Pfizer-BioNTech COVID-19 vaccination, and 0% (0 of 7; CI, 0% to 35%) versus 5% (5 of 101; CI, 2% to 11%) reported no previous mRNA COVID-19 vaccination. Lack of a placebo group, open-label study, and post hoc evaluation of urticarial risk. Urticarial reactions associated with experimental HIV-1 mRNA vaccines were observed in this trial. Studies to investigate the mechanism and approaches to mitigate these reactions are underway to further advance HIV-1 vaccine research. National Institutes of Health, National Institute of Allergy and Infectious Diseases.
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