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DNA Aß42 immunization via needle-less Jet injection in mice and rabbits as potential immunotherapy for Alzheimer's disease.
Lambracht-Washington, Doris; Fu, Min; Wight-Carter, Mary; Riegel, Matthew; Hynan, Linda S; Rosenberg, Roger N.
Afiliación
  • Lambracht-Washington D; Department of Neurology, UT Southwestern Medical Center Dallas, TX, USA. Electronic address: dlambracht-washington@retinafoundation.org.
  • Fu M; Department of Neurology, UT Southwestern Medical Center Dallas, TX, USA. Electronic address: min.fu@utsouthwestern.edu.
  • Wight-Carter M; Animal Resource Center, UT Southwestern Medical Center Dallas, TX, USA. Electronic address: mary.wight-carter@utsouthwestern.edu.
  • Riegel M; Animal Resource Center, UT Southwestern Medical Center Dallas, TX, USA; University of Kansas, Lawrence, KS, USA. Electronic address: mriegel@ku.edu.
  • Hynan LS; Departments of Population and Data Sciences (Biostatistics) & Psychiatry, UT Southwestern Medical Center Dallas, TX, USA. Electronic address: linda.hynan@utsoutwestern.edu.
  • Rosenberg RN; Department of Neurology, UT Southwestern Medical Center Dallas, TX, USA. Electronic address: roger.rosenberg@utsouthwestern.edu.
J Neurol Sci ; 446: 120564, 2023 03 15.
Article en En | MEDLINE | ID: mdl-36731358
ABSTRACT
Alzheimer's disease (AD) is the most common form of dementia found in the elderly and disease progression is associated with accumulation of Amyloid beta 1-42 (Aß42) in brain. An immune-mediated approach as a preventive intervention to reduce amyloid plaques without causing brain inflammation is highly desirable for future clinical use. Genetic immunization, in which the immunizing agent is DNA encoding Aß42, has great potential because the immune response to DNA delivered into the skin is generally non-inflammatory, and thus differs quantitatively and qualitatively from immune responses elicited by peptides, which are inflammatory with production of IFNγ and IL-17 cytokines by activated T cells. DNA immunization has historically been proven difficult to apply to larger mammals. A potential barrier to use DNA immunization in large mammals is the method for delivery of the DNA antigen. We tested jet injection in mice and rabbits and found good antibody production and safe immune responses (no inflammatory cytokines). We found significant reduction of amyloid plaques and Aß peptides in brains of the DNA Aß42 immunized 3xTg-AD mouse model. This study was designed to optimize DNA delivery for possible testing of the DNA Aß42 vaccine for AD prevention in a clinical trial.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Péptidos beta-Amiloides / Enfermedad de Alzheimer Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: J Neurol Sci Año: 2023 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Péptidos beta-Amiloides / Enfermedad de Alzheimer Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: J Neurol Sci Año: 2023 Tipo del documento: Article