Your browser doesn't support javascript.
loading
Efficacy of ABX196, a new NKT agonist, in prophylactic human vaccination.
Tefit, Josianne Nitcheu; Crabé, Sandrine; Orlandini, Bernard; Nell, Haylene; Bendelac, Albert; Deng, Shenglou; Savage, Paul B; Teyton, Luc; Serra, Vincent.
Afiliação
  • Tefit JN; Abivax, 5 rue Henri Desbruères, 91030 Evry cedex, France. Electronic address: Josianne.nitcheu@abivax.com.
  • Crabé S; Abivax, 5 rue Henri Desbruères, 91030 Evry cedex, France. Electronic address: sandrine.crabe@abivax.com.
  • Orlandini B; Phinc, 5, rue Henri Desbruères Immeuble Genavenir 8 91030 Evry, France. Electronic address: bernard.orlandini@phinc.fr.
  • Nell H; Tiervlei Trial Centre, Karl Bremer Hospital, Bellville, 7530 South Africa. Electronic address: haylenenell@ttctrials.co.za.
  • Bendelac A; Committee on Immunology and Department of Pathology, Howard Hughes Medical Institute, University of Chicago, Chicago, IL 60637, USA. Electronic address: abendela@bsd.uchicago.edu.
  • Deng S; Department of Chemistry and Biochemistry, Brigham Young University, Provo, UT 84602, USA. Electronic address: sdeng@chem.byu.edu.
  • Savage PB; Department of Chemistry and Biochemistry, Brigham Young University, Provo, UT 84602, USA. Electronic address: paul_savage@byu.edu.
  • Teyton L; Department of Immunology and Microbial science, The Scripps Research Institute, La Jolla, CA 92037, USA. Electronic address: lteyton@scripps.edu.
  • Serra V; Abivax, 5 rue Henri Desbruères, 91030 Evry cedex, France. Electronic address: vincent.serra@abivax.com.
Vaccine ; 32(46): 6138-45, 2014 Oct 21.
Article em En | MEDLINE | ID: mdl-25218293
ABSTRACT
We have assessed the immune-regulatory and adjuvant activities of a synthetic glycolipid, ABX196, a novel analog of the parental compound α-GalCer. As expected, ABX196 demonstrated a measurable and significant adjuvant effect in mice and monkeys with no appreciable toxicity at the doses used to promote immune responses. We performed a phase I/II dose escalation study of ABX196 in healthy volunteers, with the objectives to evaluate its safety profile, as well as its ability to be utilized as an adjuvant in the context of a prophylactic vaccine against hepatitis B. ABX196 was administered at three doses 0.2, 0.4, and 2.0µg, in 44 subjects. In all the individuals injected with ABX196, peripheral blood NKT cells displayed hallmarks of activation, and 45% of them had measurable circulating IFN-γ 24h after the first administration. More importantly, the addition of ABX196 to the very poorly immunogenic HBs antigen resulted in protective anti-HBs antibody responses in majority of patients, demonstrating the adjuvant properties of ABX196 in human. Further analysis of the cohort of subjects receiving ABX196 with HBs antigen also indicates that a single injection appears sufficient to provide protection. A limited set of adverse events linked to the systemic delivery of ABX196 and access to the liver, is discussed in the context of formulation and the need to limit transport of ABX196 to secondary lymphoid tissues for maximal efficacy (Eudra-CT 2012-001566-15).
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Adjuvantes Imunológicos / Vacinas contra Hepatite B / Células T Matadoras Naturais / Galactosilceramidas Tipo de estudo: Clinical_trials Limite: Adult / Animals / Humans / Male Idioma: En Revista: Vaccine Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Adjuvantes Imunológicos / Vacinas contra Hepatite B / Células T Matadoras Naturais / Galactosilceramidas Tipo de estudo: Clinical_trials Limite: Adult / Animals / Humans / Male Idioma: En Revista: Vaccine Ano de publicação: 2014 Tipo de documento: Article