Casazza Joseph P, Hofstetter Amelia R, Costner Pamela J M, Holman LaSonji A, Hendel Cynthia S, Widge Alicia T, Wu Richard L, Whalen William R, Cunningham Jennifer, Arthur Anita, Wang Xiaolin, Ola Abidemi, Saunders Jamie, Mendoza Floreliz, Novik Laura, Burgos Florez Maria C, Ortega-Villa Ana M, Apte Preeti J, Strom Larisa, Wang Lu, Imam Marjaan, Basappa Manjula, Naisan Mursal, Castro Mike, Trost Jessica F, Narpala Sandeep R, Vanderven Hillary A, Yamshchikov Galina V, Berkowitz Nina M, Gordon Ingelise J, Plummer Sarah H, Wycuff Diane L, Vazquez Sandra, Gillespie Rebecca A, Creanga Adrian, Adams William C, Carlton Kevin, Gall Jason G, McDermott Adrian B, Serebryannyy Leonid A, Houser Katherine V, Koup Richard A, Graham Barney S, Ledgerwood Julie E, Mascola John R, Pierson Theodore C, Andrews Sarah F, Kanekiyo Masaru, Dropulic Lesia K
Vaccine Research Center, National Institute of Allergy and Infectious Disease, National Institutes of Health, Bethesda, MD, 20892, USA.
U.S. Public Health Service Commissioned Corps, Rockville, MD, 20852, USA.
NPJ Vaccines. 2024 Sep 17;9(1):171. doi: 10.1038/s41541-024-00959-0.
The relative conservation of the influenza hemagglutinin (HA) stem compared to that of the immunodominant HA head makes the HA stem an attractive target for broadly protective influenza vaccines. Here we report the first-in-human, dose-escalation, open-label trial (NCT04579250) evaluating an unadjuvanted group 2 stabilized stem ferritin nanoparticle vaccine based on the H10 A/Jiangxi-Donghu/346/2013 influenza HA, H10ssF, in healthy adults. Participants received a single 20 mcg dose (n = 3) or two 60 mcg doses 16 weeks apart (n = 22). Vaccination with H10ssF was safe and well tolerated with only mild systemic and local reactogenicity reported. No serious adverse events occurred. Vaccination significantly increased homologous H10 HA stem binding and neutralizing antibodies at 2 weeks after both first and second vaccinations, and these responses remained above baseline at 40 weeks. Heterologous H3 and H7 binding antibodies also significantly increased after each vaccination and remained elevated throughout the study. These data indicate that the group 2 HA stem nanoparticle vaccine is safe and induces stem-directed binding and neutralizing antibodies.
与免疫显性的血凝素(HA)头部相比,流感血凝素(HA)茎部相对保守,这使得HA茎部成为广泛保护性流感疫苗的一个有吸引力的靶点。在此,我们报告了一项针对健康成年人的首次人体剂量递增开放标签试验(NCT04579250),该试验评估了一种基于H10 A/江西-东湖/346/2013流感HA(H10ssF)的无佐剂2组稳定茎部铁蛋白纳米颗粒疫苗。参与者接受了单次20微克剂量(n = 3)或相隔16周的两次60微克剂量(n = 22)。接种H10ssF疫苗是安全的,耐受性良好,仅报告了轻微的全身和局部反应原性。未发生严重不良事件。在首次和第二次接种后2周,接种疫苗显著增加了同源H10 HA茎部结合抗体和中和抗体,并且这些反应在40周时仍高于基线水平。每次接种后,异源H3和H7结合抗体也显著增加,并在整个研究过程中保持升高。这些数据表明,2组HA茎部纳米颗粒疫苗是安全的,并能诱导针对茎部的结合抗体和中和抗体。