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Hamster neogenin, a host-cell protein contained in a respiratory syncytial virus candidate vaccine, induces antibody responses in rabbits but not in clinical trial participants.
Steff, Ann-Muriel; Cadieux-Dion, Chanel; de Lannoy, Gaël; Prato, Maria Key; Czeszak, Xavier; André, Bruno; Ingels, Dominique C; Louckx, Marc; Dewé, Walthère; Picciolato, Marta; Maleux, Koen; Fissette, Laurence; Dieussaert, Ilse.
Afiliación
  • Steff AM; GSK , Rockville, Maryland, USA.
  • Cadieux-Dion C; GSK , Laval, Quebec, Canada.
  • de Lannoy G; GSK , Laval, Quebec, Canada.
  • Prato MK; GSK , Rixensart, Belgium.
  • Czeszak X; GSK , Rixensart, Belgium.
  • André B; GSK , Rixensart, Belgium.
  • Ingels DC; GSK , Rixensart, Belgium.
  • Louckx M; GSK , Rixensart, Belgium.
  • Dewé W; GSK , Rixensart, Belgium.
  • Picciolato M; GSK , Rixensart, Belgium.
  • Maleux K; GSK , Rixensart, Belgium.
  • Fissette L; GSK , Wavre, Belgium.
  • Dieussaert I; GSK , Wavre, Belgium.
Hum Vaccin Immunother ; 16(6): 1327-1337, 2020 06 02.
Article en En | MEDLINE | ID: mdl-31951765
ABSTRACT
A recombinant respiratory syncytial virus (RSV) fusion glycoprotein candidate vaccine (RSV-PreF) manufactured in Chinese hamster ovary cells was developed for immunization of pregnant women, to protect newborns against RSV disease through trans-placental antibody transfer. Traces of a host-cell protein, hamster neogenin (haNEO1), were identified in purified RSV-PreF antigen material. Given the high amino-acid sequence homology between haNEO1 and human neogenin (huNEO1), there was a risk that potential vaccine-induced anti-neogenin immunity could affect huNEO1 function in mother or fetus. Anti-huNEO1 IgGs were measured by enzyme-linked immunosorbent assay in sera from rabbits and trial participants (Phase 1 and 2 trials enrolling 128 men and 500 non-pregnant women, respectively; NCT01905215/NCT02360475) collected after immunization with RSV-PreF formulations containing different antigen doses with/without aluminum-hydroxide adjuvant. In rabbits, four injections administered at 14-day intervals induced huNEO1-specific IgG responses in an antigen-dose- and adjuvant-dependent manner, which plateaued in the highest-dose groups after three injections. In humans, no vaccination-induced anti-huNEO1 IgG responses were detected upon a single immunization, as the values in vaccine and control groups fluctuated around pre-vaccination levels up to 90/360 days post-vaccination. A minority of participants had anti-huNEO1 levels ≥ assay cutoff before vaccination, which did not increase post-vaccination. Thus, despite detecting vaccine-induced huNEO1-specific responses in rabbits, we found no evidence that the candidate vaccine had induced anti-huNEO1 immunity in human adults. The antigen purification process was nevertheless optimized, and haNEO1-reduced vaccines were used in a subsequent Phase 2 trial enrolling 400 non-pregnant women (NCT02956837), in which again no vaccine-induced anti-huNEO1 responses were detected.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Virus Sincitial Respiratorio Humano / Infecciones por Virus Sincitial Respiratorio / Vacunas contra Virus Sincitial Respiratorio Tipo de estudio: Clinical_trials Límite: Adult / Animals / Female / Humans / Newborn / Pregnancy Idioma: En Revista: Hum Vaccin Immunother Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Virus Sincitial Respiratorio Humano / Infecciones por Virus Sincitial Respiratorio / Vacunas contra Virus Sincitial Respiratorio Tipo de estudio: Clinical_trials Límite: Adult / Animals / Female / Humans / Newborn / Pregnancy Idioma: En Revista: Hum Vaccin Immunother Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos