NEUROBIOLOGY OF DISEASE PUBLISHES ENCOURAGING PRECLINICAL RESULTS OF AFFIRIS’ ANTIBODY MAB C6-17 TO TREAT HUNTINGTON’S DISEASE

Neurobiology of Disease publishes encouraging preclinical results of AFFiRiS’ antibody mAB C6-17 to treat Huntington’s disease

  • Monoclonal antibody mAB C6-17 targeting human/mutant huntingtin protein (HTT/mutHTT) was developed and characterized
  • In vitro assay for testing cell-to-cell transmission of mutHTT was established
  • For the first time, capability of antibody to block mutHTT transmission in vitro was demonstrated
  • Results support potential of AFFiRiS’ antibody-based concept for a new therapeutic targeting circulating extracellular mutHTT

Vienna, Austria, June 3, 2020 – AFFiRiS, a clinical-stage biotechnology company developing novel disease-modifying specific active immunotherapies (SAITs), today announced that detailed preclinical results with its monoclonal antibody mAB C6-17 to treat Huntington’s Disease (HD) were published in the peer-reviewed journal Neurobiology of Disease (https://doi.org/10.1016/j.nbd.2020.104943).

Huntington’s disease (HD) is a hereditary neurodegenerative disorder characterized by changes in personality, impairments in cognition and loss of motor function, leading to death over a period of 10 to 30 years. The disease is caused by a highly polymorphic CAG trinucleotide expansion in the gene encoding for the huntingtin protein (HTT). The resulting mutant huntingtin protein (mutHTT) is ubiquitously expressed but also exhibits the ability to propagate from cell-to-cell to disseminate pathology; a property, which may serve as a new therapeutic focus and suggest that immunotherapy may provide a viable approach to neutralize mutHTT in the extracellular space.

Accordingly, AFFiRiS set out to develop a monoclonal antibody (mAB) targeting a particularly exposed region of the HTT protein. The results published in Neurobiology of Disease show that this monoclonal antibody, designated C6-17 effectively binds mutHTT and is able to deplete the protein from cell culture supernatants. Using cell-based assays, AFFiRiS demonstrated that extracellular secretion of mutHTT into cell culture media and its subsequent uptake in recipient HeLa cells can be almost entirely blocked by mAB C6-17. Immunohistochemical stainings of post-mortem HD brain tissue confirmed the specificity of mAB C6-17 to human mutHTT aggregates.

Günther Staffler, PhD, Chief Technology Officer of AFFiRiS AG, comments: “New therapies for Huntington’s disease are urgently needed to address the root cause of this debilitating disease. Our findings demonstrate that mAB C6-17 not only successfully engages with its target, mutHTT, but also inhibits cell uptake. This suggests that the antibody could interfere with the pathological processes of mutHTT spreading in vivo. These results validate our HTT/mutHTT targeting monoclonal antibody that could ultimately be used as passive immunotherapy to treat features of Huntington’s disease.”

The majority of current preclinical and clinical mutHTT lowering strategies are based on gene silencing such as micro ribonucleic acids (miRNA) and anti-sense oligonucleotides (ASOs). These strategies are geared towards targeting mutHTT expression in the brain to interfere with the abnormal protein directly within neurons. However, mutHTT is ubiquitously expressed and antibodies would allow targeting of extracellular mutHTT throughout the body (brain and peripheral organs, tissues and plasma). This would be one of the most attractive features of this therapeutic approach.






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