KSOM study reveals potential new treatment target in the fight against COVID-19

“Our study reveals that therapy targeting GRP78 could be more effective at protecting and treating people who contract COVID-19 than vaccines alone, particularly when it comes to people who can’t get the vaccine and variants that could bypass vaccine protection but still depend on GRP78 for entry and production,” said senior author Amy S. Lee, PhD, Judy and Larry Freeman Chair in basic science research and professor at the department of biochemistry & molecular medicine.

How SARS-CoV-2 hijacks GRP78 

GRP78’s job as a chaperone molecule is to fold proteins in the endoplasmic reticulum (ER), which is a protein production factory. Upon stress, including stress caused by SARS-CoV-2 infection, GRP78 is shipped out to the cell surface. There, it facilitates binding between ACE2 and Spike protein of SARS-CoV-2, leading to enhanced viral entry. Once inside the cell, viruses are known to hijack the ER protein folding machinery, of which GRP78 is a key player, to produce more viral proteins.  

This process can be intensified in cells under stress from other diseases like diabetes or cancer, which may be one of the reasons people who have underlying health conditions are more susceptible to SARS-CoV-2 infection.

To investigate the role of GRP78 in SARS-CoV-2 infection, researchers treated lung epithelial cells with humanized monoclonal antibody (hMAb159), known to remove GRP78 from the cell surface with no adverse effects in mouse models. Intervention removed GRP78 and reduced ACE2 on the cell surface, diminishing the number of targets to which SARS-CoV-2 could attach.

These findings led researchers to conclude that interventions, such as hMAb159, to remove cell surface GRP78 could reduce SARS-CoV-2 infection and inhibit the spread and severity of COVID-19 in people who are infected.

Potential for GRP78 targeted treatment

Healthy cells need a fraction of GRP78 to function normally. However, stressed cells, such as virally infected or cancerous cells, need more GRP78 to survive and multiply, so treatments that reduce the amount of GRP78 in the body could reduce the severity of SARS-CoV-2 infection and spread without adverse effects.

While this study used a monoclonal antibody, researchers say there are other agents that could be used to reduce the amount or activity of GRP78, creating multiple pathways for potential drug solutions to target GRP78.

“What is particularly exciting for this finding is that GRP78 could be a universal target in combination with existing therapies not just to combat COVID-19, but other deadly viruses that depend on GRP78 for their infectivity as well,” said Lee.  

The next step for the research team is to explore these findings further through animal studies.  

About the study

This study was a collaborative effort among expert researchers across basic sciences, virology and experimental therapeutics. Researchers utilized USC’s Biosafety-Level 3 containment laboratory, allowing them to safely study the role of GRP78 on SARS-CoV-2 infection using live virus cultures.

In addition to Lee, the study’s authors include Parkash Gill, MD, of the department of medicine; Keigo Machida, PhD, and Da-Wei Yeh, PhD, of the department of molecular microbiology & immunology; and lead author Anthony Carlos, PhD, Dat Ha, Richard Van Krieken, PhD, Chun-Chih Tseng, PhD, and Pu Zhang of the department of biochemistry & molecular medicine.

This study was supported with grants from the National Institute of Health (R01 CA027607, R01 CA238029, R01 CA027607-37S1, R01 AA025204-01A1, R21 AA025470-01A1 and P50 AA11999) and a pilot grant from a gift by the W. M. Keck Foundation to support COVID-19 research.