Donnelly Centre Investigators are Developing Therapeutic Antibodies for Covid-19

Mar 26, 2020
Author: 
Jovana Drinjakovic

structure of the spike proteinMolecular structure of the coronavirus spike protein which Donnelly Centre investigators and their collaborators are developing neutralizing antibodies against to help boost patient immunity.

 

Donnelly Centre investigator and U of T professor Sachdev Sidhu is on a team receiving $535,318 from the federal government to engineer antibody molecules that can neutralize coronavirus in the body. The news came last week after the government decided to release more emergency funding for research that seeks to mitigate Covid-19 following the initial announcement on March 6, 2020.

Sidhu already leads a different team that received $886,090 in the first round of federal funding. The goal of that project is to design antiviral medicines that block viral replication.

“With our two funded projects, we are working to develop molecules that can target the virus both inside human cells and on the outside to prevent it from getting in,” says Sidhu.

The latest funded project, headed by U of T professor James Rini, of the Departments of Molecular Genetics and Biochemistry, aims to produce antibodies that can neutralize the virus before it invades cells. Such antibodies are naturally produced by the body in response to infection, but researchers hope to reduce the duration and severity of the disease by boosting the immune system with injected antibodies. Neutralizing antibodies are used to treat rabies, which is also caused by a virus, for example.

Other teams in Canada, as well as in the UK and US, are looking to infuse Covid-19 survivors’ blood plasma containing antibodies into patients to aid their recovery. Plasma transfusion, however, is fraught with challenges, such as variability in efficacy between different donors and risk of disease transmission. In contrast, synthetic antibodies are a defined drug in terms of molecular content, efficacy and dosing regimen.

In previous work, Rini helped to determine how antibodies bind to and inactivate the SARS virus, the coronavirus that caused the 2002-2004 outbreak in Asia. Also on the team is U of T professor Alan Cochrane, of the Department of Molecular Genetics, an HIV virologist with expertise in viral RNA processing.

"We are working to develop molecules that can target the virus both inside human cells and on the outside to prevent it from getting in" - Professor Sachdev Sidhu

The antibodies will be engineered to block the so-called S-protein that forms spikes on the virus surface. The spikes lock on to a protein called ACE2 on the surface of human cells to gain entry. Coating viral particles with synthetic antibodies should prevent the spikes from binding to ACE2.

In another approach, Sidhu and Rini will also engineer antibodies that bind ACE2 to make it inaccessible to the virus. This type of engineered immunity surpasses what is available to the natural immune system, since antibodies that react against self-proteins have been filtered out. If successful, the approach may obviate worries about viral mutations that can render drugs ineffective to new emerging viral strains, as the host protein ACE2 does not change over time.

Sidhu’s team has advanced a technology called phage display to rapidly create and select human antibodies with desired biological properties, such as blocking the virus’ spike protein. Over the last decade, his team has created hundreds of antibodies with therapeutic potential, some of which are in clinical development through spin off and large pharmaceutical companies.

Crucially, the group has demonstrated success with both approaches for inhibiting viral entry, having developed neutralizing antibodies that target the Ebola virus as well as antibodies that target the human host receptor of hanta virus or hepatitis C. Moreover, other research has shown that antibodies targeting SARS, a related virus whose genetic material is over 80 per cent identical to the one causing Covid-19, can clear infection in cells and mice.

Using phage display, in which tiny bacterial viruses called phages are instructed to create vast libraries of diverse antibodies, the team will select the antibodies that can kill the virus in human cells before testing them on mice, and eventually patients. Experiments on mice could start within three to six months, Sidhu said.

In addition to creating antibodies tailored to the new virus from scratch, the researchers will also modify existing SARS-blocking antibodies so that they attack Covid-19 and provide an additional route to the development of a therapeutic.

Given the global spread of the virus, it’s possible that it will become endemic and circulate in the population like seasonal flu. And, like the flu, it could mutate into new strains that will evade acquired immunity and the vaccines that are being developed. By generating a panel of different antibodies, the researchers aim to stay one step ahead of the virus.

“Our advances in antibody engineering technologies, and access to the complete genomes of the Covid-19 virus and its relatives, provides us with an opportunity to create tailored therapeutic antibodies at a scale and speed that was not possible even a few years ago,” says Sidhu.

“Ultimately, we aim to optimize methods to the point where the evolution of new drugs will keep pace with the evolution of the virus itself, providing new and effective drugs in response to new outbreaks.”

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