New Machine Learning-Based Approach Identifies Existing Drugs That Could Be Repurposed to Fight COVID-19

Researchers have developed a machine learning-based approach to identify drugs that might be repurposed to fight COVID-19 in elderly patients.

The machine learning-based approach developed by researchers at the Massachusetts Institute of Technology (MIT; Cambridge, MA, USA) aims to identify drugs already on the market that could potentially be repurposed to fight COVID-19, particularly in the elderly. The system accounts for changes in gene expression in lung cells caused by both the disease and aging. That combination could allow medical experts to more quickly seek drugs for clinical testing in elderly patients, who tend to experience more severe symptoms. The researchers pinpointed the protein RIPK1 as a promising target for COVID-19 drugs, and they identified three approved drugs that act on the expression of RIPK1.

Stiffening lung tissue in COVID-19 harmed older patients due to aging shows different patterns of gene expression than in younger people, even in response to the same signal. The researchers looked at aging together with SARS-CoV-2, including identifying the genes at the intersection of these two pathways. To select approved drugs that might act on these pathways, the team turned to big data and artificial intelligence.

The researchers zeroed in on the most promising drug repurposing candidates in three broad steps. First, they generated a large list of possible drugs using a machine-learning technique called an autoencoder. Next, they mapped the network of genes and proteins involved in both aging and SARS-CoV-2 infection. Finally, they used statistical algorithms to understand causality in that network, allowing them to pinpoint "upstream" genes that caused cascading effects throughout the network. In principle, drugs targeting those upstream genes and proteins should be promising candidates for clinical trials.

To generate an initial list of potential drugs, the team's autoencoder relied on two key datasets of gene expression patterns. One dataset showed how expression in various cell types responded to a range of drugs already on the market, and the other showed how expression responded to infection with SARS-CoV-2. The autoencoder scoured the datasets to highlight drugs whose impacts on gene expression appeared to counteract the effects of SARS-CoV-2. Next, the researchers narrowed the list of potential drugs by homing in on key genetic pathways. They mapped the interactions of proteins involved in the aging and Sars-CoV-2 infection pathways. Then they identified areas of overlap among the two maps. That effort pinpointed the precise gene expression network that a drug would need to target to combat COVID-19 in elderly patients.

The researchers were yet to identify which genes and proteins were "upstream" (i.e. they have cascading effects on the expression of other genes) and which were "downstream" (i.e. their expression is altered by prior changes in the network). An ideal drug candidate would target the genes at the upstream end of the network to minimize the impacts of infection. So the team used algorithms that infer causality in interacting systems to turn their undirected network into a causal network. The final causal network identified RIPK1 as a target gene/protein for potential COVID-19 drugs, since it has numerous downstream effects. The researchers identified a list of the approved drugs that act on RIPK1 and may have potential to treat COVID-19. Previously these drugs have been approved for the use in cancer. Other drugs that were also identified, including ribavirin and quinapril, are already in clinical trials for COVID-19.

The researchers now plan to share their findings with pharmaceutical companies, clinical testing is needed to determine efficacy before any of the identified drugs can be approved for repurposed use in elderly COVID-19 patients,. While this particular study focused on COVID-19, the researchers say their framework is extendable.

"I'm really excited that this platform can be more generally applied to other infections or diseases," said Anastasiya Belyaeva, study co-author and MIT PhD student.

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Massachusetts Institute of Technology (MIT)