Evaluation of an Adoptive Cellular Therapy-Based Vaccine in a Transgenic Mouse Model of α-synucleinopathy.
Winston T ChuJesse HallAnjela GurralaAlexander BecseyShreya RamanMichael S OkunCatherine T FloresBenoit I GiassonDavid E VaillancourtVinata Vedam-MaiPublished in: ACS chemical neuroscience (2022)
Aggregated α-synuclein, a major constituent of Lewy bodies plays a crucial role in the pathogenesis of α-synucleinopathies (SPs) such as Parkinson's disease (PD). PD is affected by the innate and adaptive arms of the immune system, and recently both active and passive immunotherapies targeted against α-synuclein (α-syn) are being developed and show promise as novel treatment strategies for such diseases. Specifically, dendritic cell-based vaccines have shown to be an effective treatment for SPs. Here, we report on the development of adoptive cellular therapy (ACT) for SP and demonstrate that adoptive transfer of pre-activated T-cells generated from immunized mice can improve survival and behavior, reduce brain microstructural impairment via magnetic resonance imaging (MRI), and decrease α-synuclein pathology burden in a peripherally induced preclinical SP model (M83) when administered prior to disease onset. This study provides evidence for ACT as a candidate immunotherapy for other forms of SPs.
Keyphrases
- cell therapy
- magnetic resonance imaging
- mouse model
- dendritic cells
- immune response
- stem cells
- contrast enhanced
- white matter
- mesenchymal stem cells
- parkinson disease
- computed tomography
- regulatory t cells
- diabetic rats
- cancer therapy
- machine learning
- drug induced
- bone marrow
- oxidative stress
- brain injury
- artificial intelligence
- multiple sclerosis
- deep brain stimulation
- endothelial cells