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Antibody-functionalized polymer nanoparticle leading to memory recovery in Alzheimer's disease-like transgenic mouse model.
Carradori, Dario; Balducci, Claudia; Re, Francesca; Brambilla, Davide; Le Droumaguet, Benjamin; Flores, Orfeu; Gaudin, Alice; Mura, Simona; Forloni, Gianluigi; Ordoñez-Gutierrez, Lara; Wandosell, Francisco; Masserini, Massimo; Couvreur, Patrick; Nicolas, Julien; Andrieux, Karine.
Afiliação
  • Carradori D; Institut Galien Paris Sud, CNRS UMR 8612, Univ Paris-Sud, Univ. Paris Saclay, Châtenay-Malabry, France.
  • Balducci C; Istituto Mario Negri, Milano, Italy.
  • Re F; School of Medicine and Surgery, University of Milano-Bicocca, Monza, Italy. Electronic address: francesca.re1@unimib.it.
  • Brambilla D; Institut Galien Paris Sud, CNRS UMR 8612, Univ Paris-Sud, Univ. Paris Saclay, Châtenay-Malabry, France.
  • Le Droumaguet B; Université Paris-Est, Institut de Chimie et des Matériaux Paris-Est (ICMPE), UMR 7182 CNRS-UPEC, 2 rue Henri Dunant, 94320, Thiais, France.
  • Flores O; Stab Vida, Madan Parque, Rua dos Inventores, Caparica, Portugal.
  • Gaudin A; Institut Galien Paris Sud, CNRS UMR 8612, Univ Paris-Sud, Univ. Paris Saclay, Châtenay-Malabry, France.
  • Mura S; Institut Galien Paris Sud, CNRS UMR 8612, Univ Paris-Sud, Univ. Paris Saclay, Châtenay-Malabry, France.
  • Forloni G; Istituto Mario Negri, Milano, Italy.
  • Ordoñez-Gutierrez L; Centro de Biología Molecular Severo Ochoa CSIC-UAM & CIBERNED, Madrid, Spain.
  • Wandosell F; Centro de Biología Molecular Severo Ochoa CSIC-UAM & CIBERNED, Madrid, Spain.
  • Masserini M; School of Medicine and Surgery, University of Milano-Bicocca, Monza, Italy.
  • Couvreur P; Institut Galien Paris Sud, CNRS UMR 8612, Univ Paris-Sud, Univ. Paris Saclay, Châtenay-Malabry, France.
  • Nicolas J; Institut Galien Paris Sud, CNRS UMR 8612, Univ Paris-Sud, Univ. Paris Saclay, Châtenay-Malabry, France. Electronic address: julien.nicolas@u-psud.fr.
  • Andrieux K; Faculté de Pharmacie de Paris, UTCBS, CNRS UMR 8258, Inserm U1022, Univ. Paris Descartes, Univ. Sorbonne Paris Cité, Paris, France.
Nanomedicine ; 14(2): 609-618, 2018 02.
Article em En | MEDLINE | ID: mdl-29248676
ABSTRACT
Alzheimer's disease (AD) is a neurodegenerative disorder related, in part, to the accumulation of amyloidpeptide (Aß) and especially the Aß peptide 1-42 (Aß1-42). The aim of this study was to design nanocarriers able to (i) interact with the Aß1-42 in the blood and promote its elimination through the "sink effect" and (ii) correct the memory defect observed in AD-like transgenic mice. To do so, biodegradable, PEGylated nanoparticles were surface-functionalized with an antibody directed against Aß1-42. Treatment of AD-like transgenic mice with anti-Aß1-42-functionalized nanoparticles led to (i) complete correction of the memory defect; (ii) significant reduction of the Aß soluble peptide and its oligomer level in the brain and (iii) significant increase of the Aß levels in plasma. This study represents the first example of Aß1-42 monoclonal antibody-decorated nanoparticle-based therapy against AD leading to complete correction of the memory defect in an experimental model of AD.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polímeros / Peptídeos beta-Amiloides / Modelos Animais de Doenças / Nanopartículas / Doença de Alzheimer / Transtornos da Memória / Anticorpos Monoclonais Limite: Animals / Humans / Male Idioma: En Revista: Nanomedicine Assunto da revista: BIOTECNOLOGIA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polímeros / Peptídeos beta-Amiloides / Modelos Animais de Doenças / Nanopartículas / Doença de Alzheimer / Transtornos da Memória / Anticorpos Monoclonais Limite: Animals / Humans / Male Idioma: En Revista: Nanomedicine Assunto da revista: BIOTECNOLOGIA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: França