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4th International Conference on Biochemistry & Metabolomics

Los Angeles, USA

Bill Shelander

Bill Shelander

CEO, Anven Biosciences, Inc., USA

Title: Identification of pathogenic antigen:antibody complexes of Alzheimer’s disease using “proxy antigens”
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Biography

Biography: Bill Shelander

Abstract

Alzheimer’s disease (AD) is a progressive, neurodegenerative disease and believed by many to be associated with extracellular amyloid plaques and intracellular neurofibrillary tangles1, 2.  Researchers have also long suspected that as neurodegeneration occurs in the brain, the immune response propagates disease-related antibodies in the blood, which will lastingly present in the serum of AD patients. However, despite enormous efforts through decades of research, no definitive early blood-based biomarker for AD has yet been validated3. A new approach involving “proxy antigens” provides profound new insights into the pathogenesis of Alzheimer’s disease.  By isolating the pathogenic antigen:antibody complexes directly involved in the causation and progression of Alzheimer’s, a direct biomarker of the neurodegenerative disease can measure and monitor the subject’s immune response at the earliest stages of the disease.

Proxy antigens are biosimilar, but otherwise non-native, molecules that bind to antibodies in the hypervariable region with exquisite sensitivity and specificity4-7.   Using this unprecedented capability, a systematic, step-by-step procedure first isolated the complexes unique to subjects exhibiting Alzheimer’s pathology (figure 1).  Thereafter, the Alzheimer’s-specific proxy antigens provide a clear diagnostic tool to detect whether the Alzheimer’s complexes are present or absent in blood samples.  One high value application of AD-specific proxy antigens can profile and stratify clinical trial populations, i.e. differentiate and predict which subjects would respond to a drug and which would not.  For example, retrospective analysis of archived blood samples from a past clinical trial can be used to unambiguously reassess subgroups of subjects and offer an enriched population for a guided prospective clinical trial. Additionally, and perhaps most importantly, the identified Alzheimer’s complexes provide definitive targets for future therapeutic development.