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Immunotherapeutic Approaches Targeting Amyloid-beta, alpha-Synuclein, and Tau for the Treatment of Neurodegenerative Disorders

Journal

NEUROTHERAPEUTICS
Volume 13, Issue 1, Pages 179-189

Publisher

SPRINGER
DOI: 10.1007/s13311-015-0397-z

Keywords

Immunotherapy; Vaccines; Antibodies; Amyloid-beta; alpha-synuclein; Tau

Funding

  1. National Institutes of Health (NIH) [AG18440, AG022074, NS044233]
  2. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [P01NS044233] Funding Source: NIH RePORTER
  3. NATIONAL INSTITUTE ON AGING [P50AG005131, R01AG018440, P01AG022074, R37AG018440] Funding Source: NIH RePORTER

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Disease-modifying alternatives are sorely needed for the treatment of neurodegenerative disorders, a group of diseases that afflict approximately 50 million Americans annually. Immunotherapy is one of the most developed approaches in this direction. Vaccination against amyloid-beta, asynuclein, or tau has been extensively explored, specially as the discovery that these proteins may propagate cell-to-cell and be accessible to antibodies when embedded into the plasma membrane or in the extracellular space. Likewise, the use of passive immunization approaches with specific antibodies against abnormal conformations of these proteins has also yielded promising results. The clinical development of immunotherapies for Alzheimer's disease, Parkinson's disease, frontotemporal dementia, dementia with Lewy bodies, and other neurodegenerative disorders is a field in constant evolution. Results to date suggest that immunotherapy is a promising therapeutic approach for neurodegenerative diseases that progress with the accumulation and prion-like propagation of toxic protein aggregates. Here we provide an overview of the most novel and relevant immunotherapeutic advances targeting amyloid-beta in Alzheimer's disease, alpha-synuclein in Alzheimer's disease and Parkinson's disease, and tau in Alzheimer's disease and frontotemporal dementia.

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