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Targeting isoaspartate-modified Aβ rescues behavioral deficits in transgenic mice with Alzheimer's disease-like pathology.

Kathrin GnothAnke PiechottaMartin KleinschmidtSandra KonrathMathias SchenkNadine TaudteDaniel RamsbeckVera RieckmannStefanie GeisslerRico EichentopfSusan BarendrechtMaike Hartlage-RübsamenHans-Ulrich DemuthSteffen RoßnerHolger CynisJens-Ulrich RahfeldStephan Schilling
Published in: Alzheimer's research & therapy (2020)
The present study demonstrates, for the first time, that the antibody-mediated targeting of isoD7-modified Aβ peptides leads to attenuation of AD-like amyloid pathology. In conjunction with previously published data on antibodies directed against pGlu-modified Aβ, the results highlight the crucial role of modified Aβ peptides in AD pathophysiology. Hence, the results also underscore the therapeutic potential of targeting modified amyloid species for defining tailored approaches in AD therapy.
Keyphrases
  • cancer therapy
  • traumatic brain injury
  • randomized controlled trial
  • systematic review
  • cognitive decline
  • drug delivery
  • mesenchymal stem cells
  • mouse model
  • mild cognitive impairment
  • genetic diversity