What is it about?

Perspectives of targeting neuropilin 1: Role in Viral Entry: NRP1 enhances the entry of SARS-CoV-2 into host cells by binding to the Spike protein’s furin-cleaved S1 fragment. This interaction is crucial for the virus’s infectivity and spread. Therapeutic Potential: By targeting NRP1, it may be possible to reduce the efficiency of viral entry, thereby decreasing the overall viral load and severity of the infection. Potential Approaches: Small Molecule Inhibitors: Researchers are exploring small molecules that can block the interaction between NRP1 and the Spike protein. Some compounds have shown promise in disrupting this binding and reducing viral entry in preclinical studies. Monoclonal Antibodies: Developing antibodies that specifically target NRP1 could prevent the virus from using this pathway to enter cells. This approach is similar to how some current COVID-19 treatments target the Spike protein itself. RNA Interference: Using RNA interference to downregulate NRP1 expression in host cells could be another strategy to reduce viral entry and replication. Combination Therapies: Combining NRP1 inhibitors with other antiviral treatments could enhance overall efficacy, potentially leading to better clinical outcomes.

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Why is it important?

Targeting neuropilin 1 (NRP1) in SARS-CoV-2 infection is an emerging area of interest due to its role as a co-receptor that facilitates viral entry into host cells. We outlined here some perspectives and potential approaches.

Perspectives

All outlined strategies are still in the research phase, but they offer promising avenues for developing new treatments against COVID-19 and potentially against other emerging pathogen where NRP1 may play a role as a virus entry/co-entry receptor.

Svetlana Chapoval
University of Maryland School of Medicine

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This page is a summary of: Perspectives and potential approaches for targeting neuropilin 1 in SARS-CoV-2 infection, Extremophiles, December 2021, Springer Science + Business Media,
DOI: 10.1186/s10020-021-00423-y.
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