Targeting amyotrophic lateral sclerosis by neutralizing seeding-competent TDP-43 in CSF

Author:

Audrain Mickael1ORCID,Egesipe Anne-Laure1,Tentillier Noémie1ORCID,Font Laure1,Ratnam Monisha1,Mottier Lorene1,Clavel Mathieu1,Le Roux-Bourdieu Morgan1,Fenyi Alexis1,Ollier Romain1,Chevalier Elodie1,Guilhot Florence1,Fuchs Aline1,Piorkowska Kasia1,Carlyle Becky2ORCID,Arnold Steven E3,Berry James D4,Luthi-Carter Ruth1,Adolfsson Oskar1ORCID,Pfeifer Andrea1,Kosco-Vilbois Marie1,Seredenina Tamara1,Afroz Tariq1ORCID

Affiliation:

1. Research, AC Immune SA , 1015 Lausanne , Switzerland

2. Department of Physiology, Anatomy and Genetics, University of Oxford , Oxford OX1 3PT , UK

3. Department of Neurology and the Massachusetts Alzheimer’s Disease Research Center, Massachusetts General Hospital, Harvard Medical School , Boston, MA 02129 , USA

4. Sean M. Healey & AMG Center for ALS & the Neurological Clinical Research Institute, Massachusetts General Hospital, Harvard Medical School , Boston, MA 02114 , USA

Abstract

Abstract In amyotrophic lateral sclerosis, a disease driven by abnormal transactive response DNA-binding protein of 43 kDa aggregation, CSF may contain pathological species of transactive response DNA-binding protein of 43 kDa contributing to the propagation of pathology and neuronal toxicity. These species, released in part by degenerating neurons, would act as a template for the aggregation of physiological protein contributing to the spread of pathology in the brain and spinal cord. In this study, a robust seed amplification assay was established to assess the presence of seeding-competent transactive response DNA-binding protein of 43 kDa species in CSF of apparently sporadic amyotrophic lateral sclerosis patients. These samples resulted in a significant acceleration of substrate aggregation differentiating the kinetics from healthy controls. In parallel, a second assay was developed to determine the level of target engagement that would be necessary to neutralize such species in human CSF by a therapeutic monoclonal antibody targeting transactive response DNA-binding protein of 43 kDa. For this, evaluation of the pharmacokinetic/pharmacodynamic effect for the monoclonal antibody, ACI-5891.9, in vivo and in vitro confirmed that a CSF concentration of ≍1100 ng/mL would be sufficient for sustained target saturation. Using this concentration in the seed amplification assay, ACI-5891.9 was able to neutralize the transactive response DNA-binding protein of 43 kDa pathogenic seeds derived from amyotrophic lateral sclerosis patient CSF. This translational work adds to the evidence of transmission of transactive response DNA-binding protein of 43 kDa pathology via CSF that could contribute to the non-contiguous pattern of clinical manifestations observed in amyotrophic lateral sclerosis and demonstrates the ability of a therapeutic monoclonal antibody to neutralize the toxic, extracellular seeding-competent transactive response DNA-binding protein of 43 kDa species in the CSF of apparently sporadic amyotrophic lateral sclerosis patients.

Funder

AC Immune SA

Publisher

Oxford University Press (OUP)

Subject

Neurology,Cellular and Molecular Neuroscience,Biological Psychiatry,Psychiatry and Mental health

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