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Towards a nanoparticle-based prophylactic for maternal autoantibody-related autism.


ABSTRACT: Recently, the causative agents of Maternal Autoantibody-Related (MAR) autism, pathological autoantibodies and their epitopic targets (e.g. lactate dehydrogenase B [LDH B] peptide), have been identified. Herein, we report on the development of Systems for Nanoparticle-based Autoantibody Reception and Entrapment (SNAREs), which we hypothesized could scavenge disease-propagating MAR autoantibodies from the maternal blood. To demonstrate this functionality, we synthesized 15?nm dextran iron oxide nanoparticles surface-modified with citric acid, methoxy PEG(10?kDa) amine, and LDH B peptide (33.8??g peptide/cm2). In vitro, we demonstrated significantly lower macrophage uptake for SNAREs compared to control NPs. The hallmark result of this study was the efficacy of the SNAREs to remove 90% of LDH B autoantibody from patient-derived serum. Further, in vitro cytotoxicity testing and a maximal tolerated dose study in mice demonstrated the safety of the SNARE formulation. This work establishes the feasibility of SNAREs as the first-ever prophylactic against MAR autism.

SUBMITTER: Bolandparvaz A 

PROVIDER: S-EPMC7197945 | biostudies-literature | 2019 Oct

REPOSITORIES: biostudies-literature

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Towards a nanoparticle-based prophylactic for maternal autoantibody-related autism.

Bolandparvaz Amir A   Harriman Rian R   Alvarez Kenneth K   Lilova Kristina K   Zang Zexi Z   Lam Andy A   Edmiston Elizabeth E   Navrotsky Alexandra A   Vapniarsky Natalia N   Van De Water Judy J   Lewis Jamal S JS  

Nanomedicine : nanotechnology, biology, and medicine 20190723


Recently, the causative agents of Maternal Autoantibody-Related (MAR) autism, pathological autoantibodies and their epitopic targets (e.g. lactate dehydrogenase B [LDH B] peptide), have been identified. Herein, we report on the development of Systems for Nanoparticle-based Autoantibody Reception and Entrapment (SNAREs), which we hypothesized could scavenge disease-propagating MAR autoantibodies from the maternal blood. To demonstrate this functionality, we synthesized 15 nm dextran iron oxide na  ...[more]

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