Abstract
Recent studies have been demonstrated that host immune imbalance is an important factors leading to acute respiratory
distress syndrome (ARDS) in COVID-19 patients. Therefore, discovery of potential drugs and identification of their mechanisms of action
for the prevention of immune imbalance in COVID-19 patients are urgently needed. In this study, we proposed a network representation
learning-based methodology, termed AIdrug2cov, to discover drug mechanism and anti-inflammatory response for patients with COVID19. In AIdrug2cov, a deep bidirectional Transformer encoder network representation approach is developed to automatically learn lowdimensional vector of heterogeneous network. Using the representation vectors, AIdrug2cov identifies 40 potential targets and 24
high-confidence drugs that bind to tumor necrosis factor(TNF)-α or interleukin(IL)-6 to prevent excessive inflammatory responses in
COVID-19 patients. In particular, AIdrug2cov indicated that chloroquine and hydroxychloroquine are able to reduce fatality of COVID-19
patients, and that their mechanisms of action are likely mediated through their inhibition of inflammatory cytokines on top of their antiviral
ability, consistent with the findings of clinical studies. In addition, the results in 5 pharmacological application suggested that AIdrug2cov
significantly outperforms 5 other state-of-the-art network representation approaches, future demonstrating the availability of AIdrug2cov
in drug development field. In summary, AIdrug2cov is practically useful for accelerating COVID-19 therapeutic development. The source
code and data can be downloaded from https://github.com/pengsl-lab/AIdrug2cov.git