TY - JOUR
T1 - Safety and immunogenicity of a ferritin nanoparticle H2 influenza vaccine in healthy adults
T2 - a phase 1 trial
AU - the VRC 316 Study Team
AU - Houser, Katherine V.
AU - Chen, Grace L.
AU - Carter, Cristina
AU - Crank, Michelle C.
AU - Nguyen, Thuy A.
AU - Burgos Florez, Maria Claudia
AU - Berkowitz, Nina M.
AU - Mendoza, Floreliz
AU - Hendel, Cynthia Starr
AU - Gordon, Ingelise J.
AU - Coates, Emily E.
AU - Vazquez, Sandra
AU - Stein, Judy
AU - Case, Christopher L.
AU - Lawlor, Heather
AU - Carlton, Kevin
AU - Gaudinski, Martin R.
AU - Strom, Larisa
AU - Hofstetter, Amelia R.
AU - Liang, C. Jason
AU - Narpala, Sandeep
AU - Hatcher, Christian
AU - Gillespie, Rebecca A.
AU - Creanga, Adrian
AU - Kanekiyo, Masaru
AU - Raab, Julie E.
AU - Andrews, Sarah F.
AU - Zhang, Yi
AU - Yang, Eun Sung
AU - Wang, Lingshu
AU - Leung, Kwanyee
AU - Kong, Wing Pui
AU - Freyn, Alec W.
AU - Nachbagauer, Raffael
AU - Palese, Peter
AU - Bailer, Robert T.
AU - McDermott, Adrian B.
AU - Koup, Richard A.
AU - Gall, Jason G.
AU - Arnold, Frank
AU - Mascola, John R.
AU - Graham, Barney S.
AU - Ledgerwood, Julie E.
AU - Casazza, Joseph
AU - Holman, Lasonji
AU - Ola, Abidemi O.
AU - Costner, Pamela
AU - Cunningham, Jennifer
AU - Larkin, Brenda
AU - Novik, Laura
N1 - Funding Information:
We thank the trial participants for their involvement as well as PharmaJet for the use of the needle-free Stratis device in this clinical trial. This work was supported by intramural funding from the National Institute of Allergy and Infectious Diseases (NIAID) through the National Institutes of Health (NIH) Intramural Research Program (K.V.H., G.L.C., C.C., M.C.C., T.A.N., M.C.B.F., N.M.B., F.M., C.S.H., I.J.G., E.E.C., S.V., J.S., C.L.C., H.L., K.C., M.R.G., L.S., A.R.H., C.J.L., S.N., C.H., R.A.G., A.C., M.K., J.E.R., S.F.A., Y.Z., E.S.Y., L.W., K.L., W-P.K., R.T.B., A.B.M., R.A.K., J.G.G., F.A., J.R.M., B.S.G. and J.E.L.). This work was partially funded by the NIAID-funded Centers of Excellence for Influenza Research and Response (75N93021C00014, to A.W.F., R.N. and P.P.), by NIAID grant P01 AI097092-07 (to A.W.F., R.N. and P.P.), by NIAID grant R01 AI145870-03 (to A.W.F., R.N. and P.P.) and by the Collaborative Vaccine Innovation Centers contract 75N93019C00051 (to A.W.F., R.N. and P.P.). The Vaccine Research Center (VRC) and its investigators had complete control over study conceptualization and design, data collection and analysis, decision to publish and preparation of this manuscript. Study team representative: Floreliz Mendoza, VRC, NIAID, NIH (email: floreliz.mendoza@nih.gov; phone: 301-451-8715).
Funding Information:
We thank the trial participants for their involvement as well as PharmaJet for the use of the needle-free Stratis device in this clinical trial. This work was supported by intramural funding from the National Institute of Allergy and Infectious Diseases (NIAID) through the National Institutes of Health (NIH) Intramural Research Program (K.V.H., G.L.C., C.C., M.C.C., T.A.N., M.C.B.F., N.M.B., F.M., C.S.H., I.J.G., E.E.C., S.V., J.S., C.L.C., H.L., K.C., M.R.G., L.S., A.R.H., C.J.L., S.N., C.H., R.A.G., A.C., M.K., J.E.R., S.F.A., Y.Z., E.S.Y., L.W., K.L., W-P.K., R.T.B., A.B.M., R.A.K., J.G.G., F.A., J.R.M., B.S.G. and J.E.L.). This work was partially funded by the NIAID-funded Centers of Excellence for Influenza Research and Response (75N93021C00014, to A.W.F., R.N. and P.P.), by NIAID grant P01 AI097092-07 (to A.W.F., R.N. and P.P.), by NIAID grant R01 AI145870-03 (to A.W.F., R.N. and P.P.) and by the Collaborative Vaccine Innovation Centers contract 75N93019C00051 (to A.W.F., R.N. and P.P.). The Vaccine Research Center (VRC) and its investigators had complete control over study conceptualization and design, data collection and analysis, decision to publish and preparation of this manuscript. Study team representative: Floreliz Mendoza, VRC, NIAID, NIH (email: floreliz.mendoza@nih.gov; phone: 301-451-8715).
Publisher Copyright:
© 2022, This is a U.S. government work and not under copyright protection in the U.S.; foreign copyright protection may apply.
PY - 2022/2
Y1 - 2022/2
N2 - Currently, licensed seasonal influenza vaccines display variable vaccine effectiveness, and there remains a need for novel vaccine platforms capable of inducing broader responses against viral protein domains conserved among influenza subtypes. We conducted a first-in-human, randomized, open-label, phase 1 clinical trial (NCT03186781) to evaluate a novel ferritin (H2HA-Ferritin) nanoparticle influenza vaccine platform. The H2 subtype has not circulated in humans since 1968. Adults born after 1968 have been exposed to only the H1 subtype of group 1 influenza viruses, which shares a conserved stem with H2. Including both H2-naive and H2-exposed adults in the trial allowed us to evaluate memory responses against the conserved stem domain in the presence or absence of pre-existing responses against the immunodominant HA head domain. Fifty healthy participants 18–70 years of age received H2HA-Ferritin intramuscularly as a single 20-μg dose (n = 5) or a 60-μg dose either twice in a homologous (n = 25) prime-boost regimen or once in a heterologous (n = 20) prime-boost regimen after a matched H2 DNA vaccine prime. The primary objective of this trial was to evaluate the safety and tolerability of H2HA-Ferritin either alone or in prime-boost regimens. The secondary objective was to evaluate antibody responses after vaccination. Both vaccines were safe and well tolerated, with the most common solicited symptom being mild headache after both H2HA-Ferritin (n = 15, 22%) and H2 DNA (n = 5, 25%). Exploratory analyses identified neutralizing antibody responses elicited by the H2HA-Ferritin vaccine in both H2-naive and H2-exposed populations. Furthermore, broadly neutralizing antibody responses against group 1 influenza viruses, including both seasonal H1 and avian H5 subtypes, were induced in the H2-naive population through targeting the HA stem. This ferritin nanoparticle vaccine technology represents a novel, safe and immunogenic platform with potential application for pandemic preparedness and universal influenza vaccine development.
AB - Currently, licensed seasonal influenza vaccines display variable vaccine effectiveness, and there remains a need for novel vaccine platforms capable of inducing broader responses against viral protein domains conserved among influenza subtypes. We conducted a first-in-human, randomized, open-label, phase 1 clinical trial (NCT03186781) to evaluate a novel ferritin (H2HA-Ferritin) nanoparticle influenza vaccine platform. The H2 subtype has not circulated in humans since 1968. Adults born after 1968 have been exposed to only the H1 subtype of group 1 influenza viruses, which shares a conserved stem with H2. Including both H2-naive and H2-exposed adults in the trial allowed us to evaluate memory responses against the conserved stem domain in the presence or absence of pre-existing responses against the immunodominant HA head domain. Fifty healthy participants 18–70 years of age received H2HA-Ferritin intramuscularly as a single 20-μg dose (n = 5) or a 60-μg dose either twice in a homologous (n = 25) prime-boost regimen or once in a heterologous (n = 20) prime-boost regimen after a matched H2 DNA vaccine prime. The primary objective of this trial was to evaluate the safety and tolerability of H2HA-Ferritin either alone or in prime-boost regimens. The secondary objective was to evaluate antibody responses after vaccination. Both vaccines were safe and well tolerated, with the most common solicited symptom being mild headache after both H2HA-Ferritin (n = 15, 22%) and H2 DNA (n = 5, 25%). Exploratory analyses identified neutralizing antibody responses elicited by the H2HA-Ferritin vaccine in both H2-naive and H2-exposed populations. Furthermore, broadly neutralizing antibody responses against group 1 influenza viruses, including both seasonal H1 and avian H5 subtypes, were induced in the H2-naive population through targeting the HA stem. This ferritin nanoparticle vaccine technology represents a novel, safe and immunogenic platform with potential application for pandemic preparedness and universal influenza vaccine development.
UR - http://www.scopus.com/inward/record.url?scp=85124733879&partnerID=8YFLogxK
U2 - 10.1038/s41591-021-01660-8
DO - 10.1038/s41591-021-01660-8
M3 - Article
C2 - 35115706
AN - SCOPUS:85124733879
SN - 1078-8956
VL - 28
SP - 383
EP - 391
JO - Nature Medicine
JF - Nature Medicine
IS - 2
ER -