Researchers have designed constructs by adding more glycans and adding the receptor-binding motif from related sarbecoviruses to focus the immune response to the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) receptor-binding motif. Such immunogens could potentially also neutralize other variants and coronaviruses.
When infected by viruses, either by natural infection or vaccination, the human immune system responds by targeting glycoproteins on the virus’s surface. This can provide protection when infected again by the same or similar virus.
However, for some infections like influenza or human immunodeficiency virus (HIV), the immune system targets different viral epitopes, leading to inadequate protection. The immune response can also decrease over time, leading to the possibility of reinfection, like in the case of the common cold.
For SARS-CoV-2, previous infection or vaccination seems to provide reduced protection against new variants, and it is still unknown if vaccines protect from infection in the long-term.
Some immunogen design strategies try to direct the immune response by “masking” epitopes or designing protein scaffolds for broad protective epitopes. Such designs could also be used for SARS-CoV-2. The possible target could be the part of the virus receptor-binding domain (RBD) that binds to the human receptor, the angiotensin-converting enzyme 2 (ACE2), a functionally conserved epitope. This may also reduce the chance of viral escape, preventing the virus from mutating.
Engineering receptor binding motif
In a new research paper published on the bioRxiv* preprint server, researchers report modifying the RBD by hyperglycosylation and attaching the RBD receptor binding motif (RBM) from SARS-CoV-2 to other coronavirus RBDs, which will focus serum response to the RBM.
The RBM of SARS-CoV-2 and related sarbecoviruses spans residues 437–502. The researchers expressed the SARS-CoV-2 RBM without the rest of the RBD, but it failed to attach to ACE2 expressed in cells or an RBM-specific antibody B38. This suggests the RBM is conformationally flexible, and the RBD stabilizes it in a conformation compatible with binding.
Resurfacing and hyperglycosylation approaches for immune-focusing. (A) Design schematic for resurfacing SARS-1 (rsSARS-1) and WIV1 (rsWIV1 ) with the SARS-2 receptor binding motif (RBM). Design schematic for hyperglycosylating SARS-2 (B), rsSARS-1 (C) and rsWIV1 (D) receptor binding domains (RBDs). Non-native engineered glycans and native glycans are modeled; native SARS-2 RBM glycan at position 331 is omitted in the schematic. Mutations in the WIV1 and SARS-1 RBDs are shown in red and italicized in the linear diagram. All images were created using PDB 6M0J.
So, the researchers grafted the SARS-CoV-2 RBM to SARS-CoV and WIV-1, another sarbecovirus, RBDs. These resurfaced constructs bound to both B38 antibody and ACE2.
The team next introduced more glycans, in addition to those conserved in the different viruses, onto the wild-type SARS-CoV-2 and the resurfaces viruses. The hyperglycosylated constructs behaved similarly to the native RBM, with a 2-fold decrease in affinity to B38, and were also able to attach to ACE2.
They tested the effect of these engineered glycosylated viruses on cross-reactive sarbecovirus antibodies S309 and CR3022 isolated from SARS-CoV convalescent patients. Hyperglycosylated SARS-CoV-2 prevented binding these antibodies, while the resurface hyperglycosylated SARS-CoV and WIV1 allowed some antibody binding. So, the team added some mutations on these constructs to prevent any cross-reactivity between antibodies to them.
Recognition of mutations possible
Using a murine model, the researchers tested the RBM immune focusing of the constructs. They found all the constructs produced antibodies to wild-type SARS-CoV-2 RBD, with the mixture of the hyperglycosylated and resurfaced constructs showing better RBM immune focusing compared to the only hyperglycosylated construct.
Both these also had lower antibody titers to SARS-CoV-1 and WIV1 RBDS compared to SARS-CoV-2 RBD. This suggests that the engineered designs could reduce response to areas outside the RBM shared by the viruses.
All the constructs elicited strong neutralization to SARS-CoV-2. The hyperglycosylated construct and the mixture also showed a neutralization response to SARS-CoV-1 and WIV1. WIV1 is a representative for emerging sarbecoviruses that can potentially create another pandemic. Thus, the constructs can also produce cross-reactive antibodies that bind to a conserved RBM epitope.
The new variants of SARS-CoV-2 detected first in the United Kingdom, South Africa, and Brazil all have mutations in the RBM. All the designed constructs showed no significant loss of binding to the South African variant compared to the wild-type virus.
This observed neutralization response suggests immune focusing to the RBM may allow for greater recognition of different mutations compared to the antibody response elicited by natural infection or vaccination.
The results show that designing immunogens can be a strategy to improve RBM-directed immune response. The strategy allows for eliciting antibodies that neutralize not only the initial SARS-CoV-2 but also the emerging variants and coronaviruses that have the potential to create another pandemic. These approaches can also be used for other types of viruses, apart from coronaviruses, as a general strategy to elicit a neutralizing antibody response to conserved epitopes.
bioRxiv publishes preliminary scientific reports that are not peer-reviewed and, therefore, should not be regarded as conclusive, guide clinical practice/health-related behavior, or treated as established information.