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ProMIS Neurosciences Inc PMN

ProMIS Neurosciences Inc. is a clinical-stage biotechnology company. It is focused on generating and developing antibody therapeutics selectively targeting toxic misfolded proteins in neurodegenerative diseases such as Alzheimer’s disease (AD), amyotrophic lateral sclerosis (ALS) and multiple system atrophy (MSA). Its proprietary target discovery engine applies a thermodynamic, computational discovery platform-ProMIS and Collective Coordinates-to predict novel targets known as Disease Specific Epitopes on the molecular surface of misfolded proteins. Using this approach, the Company is developing novel antibody therapeutics for AD, ALS and MSA. Its product candidates are PMN310, PMN267, and PMN442. The PMN310 is a monoclonal antibody designed to treat AD by selectively targeting toxic, misfolded oligomers of amyloid-beta. PMN267 product candidate targeting ALS. PMN442 is a drug candidate being developed for MSA designed to selectively target and protect against pathogenic a-syn species.


NDAQ:PMN - Post by User

Post by retiredcopon Oct 16, 2022 1:19pm
247 Views
Post# 35027769

New information coming out everyday

New information coming out everyday
Researchers Have a New Theory About What Causes Alzheimer's, And It's Not Plaque
HEALTH
15 October 2022
ByANDREA STURCHIO ET AL., THE CONVERSATION
 
An illustration of a degenerating neuron. (CIPhotos/iStock/Getty Images)
In 1906, Alois Alzheimer, a psychiatrist and neuroanatomist, reported "a peculiar severe disease process of the cerebral cortex" to a gathering of psychiatrists in Tbingen, Germany.
 
 
The case was a 50-year-old woman who suffered from memory loss, delusions, hallucinations, aggression, and confusion – all of which worsened until her untimely death five years later.
 
In the autopsy, Alzheimer noticed distinctive plaques on her brain. These plaques – clumps of amyloid-beta protein – are still considered to be the cause of Alzheimer's disease.
 
However, this theory has two major problems.
 
First, it does not explain why many subjects (even old people) have plaques in their brains in the absence of any neurological symptoms, such as memory loss.
 
Second, clinical trials for drugs that reduce these plaques have been unsuccessful – with one recent exception, but more of that later.
 
When amyloid-beta protein accumulates in the form of plaques (insoluble clumps), the original soluble form of the protein, which performs important functions in the brain, is consumed and lost.
 
 
Some studies have shown that reduced levels of soluble amyloid-beta – called amyloid-beta 42 – have led to patients having worse clinical outcomes.
 
In a recent study, published in the Journal of Alzheimer's Disease, we investigated whether it's the amount of plaques in the brain or the amount of amyloid-beta 42 remaining that is more important for Alzheimer's disease progression.
 
To answer this question, we studied data on a group of people who have a rare inherited gene mutation that puts them at high risk of developing Alzheimer's disease. The participants were from the Dominantly Inherited Alzheimer Network cohort study.
 
We found that the depletion of amyloid-beta 42 (the functional version of amyloid-beta) is more harmful than the amount of plaques (the insoluble clumps of amyloid beta).
 
 
Participants had an average of three years follow-up and we found that those with high levels of amyloid-beta 42 in their cerebrospinal fluid (the liquid around the brain and spinal cord) were protected and their cognition was preserved over the study period.
 
This chimes with many studies that showed important functions of amyloid-beta 42 in memory and cognition.
 
It is also relevant because we studied people with the genetic mutation who develop Alzheimer's disease, a group that is considered to provide the strongest evidence supporting the idea that amyloid-beta plaques are harmful.
 
However, even in this group, those with higher cerebrospinal fluid (CSF) levels of amyloid-beta 42 remained cognitively normal regardless of the amount of plaques in their brains.
 
It is also worth mentioning that in some rare, inherited forms of Alzheimer's disease – for example, in carriers of the so-called Osaka gene mutation or Arctic mutation – people can develop dementia having low levels of amyloid-beta 42 and no detectable plaques.
 
 
This suggests that plaques aren't the cause of their dementia, but low levels of amyloid-beta 42 might be.
 
Lecanemab – the one recent exception
How will our findings affect drug development and clinical trials for Alzheimer's disease? Until the recent trial with lecanemab, an antibody drug that reduces plaques, all the drug trials in Alzheimer's disease have failed.
 
Some drugs were designed to reduce the levels of amyloid-beta 42, based on the rationale that if levels of the normal protein are reduced, patients will accumulate fewer plaques. Unfortunately, these drugs often made the patient's condition worse.
 
Lecanemab was recently reported to have a small but significant effect in reducing cognitive decline. According to previous studies, this drug increases the levels of amyloid-beta 42 in the CSF.
 
 
This is, again, in line with our hypothesis, namely that the increase of the normal amyloid protein can be beneficial.
 
We will know more when the results of the lecanemab trial are published. At the moment, all we have is a press release from the makers of the drug.
 
We think that it will be important for future trials to focus on the levels of amyloid-beta 42, and whether it is beneficial to increase and restore its levels to normal values instead of targeting it for removal.
 
This could be achieved using proteins similar to amyloid-beta 42 – so-called "protein analogs" – but that clump together less than the natural ones.
 
This active protein replacement approach might become a promising new avenue of treatment for Alzheimer's and other protein aggregation diseases, such as Parkinson's and motor neuron disease.
 
Andrea Sturchio, MD, PhD Student, Clinical Neuroscience, Karolinska Institutet; Kariem Ezzat, Research Scientist, Laboratory Medicine, Karolinska Institutet, and Samir EL Andaloussi, Professor, Laboratory Medicine, Karolinska Institutet
 
This article is republished from The Conversation under a Creative Commons license. Read the original article.
 
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