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Amyloid-ß targeting immunisation in aged non-human primate (Microcebus murinus).
Trouche, Stéphanie G; Boutajangout, Allal; Asuni, Ayodeji; Fontés, Pascaline; Sigurdsson, Einar M; Verdier, Jean-Michel; Mestre-Francés, Nadine.
Afiliação
  • Trouche SG; MMDN, Univ Montpellier, EPHE, INSERM, Montpellier, France; PSL Research University, Paris, France. Electronic address: stephanie.Sabatier@icm.unicancer.fr.
  • Boutajangout A; Departments of Neurology, and Neuroscience and Physiology, New York University Grossman School of Medicine, New York, United States. Electronic address: Allal.Boutajangout@nyulangone.org.
  • Asuni A; Department of Psychiatry, New York University Grossman School of Medicine, New York, United States. Electronic address: asuni@mac.com.
  • Fontés P; MMDN, Univ Montpellier, EPHE, INSERM, Montpellier, France. Electronic address: pascaline.fontes@umontpellier.fr.
  • Sigurdsson EM; Departments of Neuroscience and Physiology, and Psychiatry, Neuroscience Institute, New York University Grossman School of Medicine, New York, United States. Electronic address: Einar.Sigurdsson@nyulangone.org.
  • Verdier JM; MMDN, Univ Montpellier, EPHE, INSERM, Montpellier, France; PSL Research University, Paris, France. Electronic address: jean-michel.verdier@ephe.psl.eu.
  • Mestre-Francés N; MMDN, Univ Montpellier, EPHE, INSERM, Montpellier, France; PSL Research University, Paris, France. Electronic address: nadine.frances@umontpellier.fr.
Brain Behav Immun ; 109: 63-77, 2023 03.
Article em En | MEDLINE | ID: mdl-36592872
ABSTRACT
Non-human primates have an important translational value given their close phylogenetic relationship to humans. Studies in these animals remain essential for evaluating efficacy and safety of new therapeutic approaches, particularly in aging primates that display Alzheimer's disease (AD) -like pathology. With the objective to improve amyloid-ß (Aß) targeting immunotherapy, we investigated the safety and efficacy of an active immunisation with an Aß derivative, K6Aß1-30-NH2, in old non-human primates. Thirty-two aged (4-10 year-old) mouse lemurs were enrolled in the study, and received up to four subcutaneous injections of the vaccine in alum adjuvant or adjuvant alone. Even though antibody titres to Aß were not high, pathological examination of the mouse lemur brains showed a significant reduction in intraneuronal Aß that was associated with reduced microgliosis, and the vaccination did not lead to microhemorrhages. Moreover, a subtle cognitive improvement was observed in the vaccinated primates, which was probably linked to Aß clearance. This Aß derivative vaccine appeared to be safe as a prophylactic measure based on the brain analyses and because it did not appear to have detrimental effects on the general health of these old animals.
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Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 2_ODS3 Base de dados: MEDLINE Assunto principal: Vacinas / Cheirogaleidae / Doença de Alzheimer Limite: Animals Idioma: En Revista: Brain Behav Immun Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 2_ODS3 Base de dados: MEDLINE Assunto principal: Vacinas / Cheirogaleidae / Doença de Alzheimer Limite: Animals Idioma: En Revista: Brain Behav Immun Ano de publicação: 2023 Tipo de documento: Article