Aiming to stop a range of coronaviruses
By ROCKEFELLER UNIVERSITY
Researchers in Japan have developed a vaccination strategy in mice that promotes the production of antibodies that can neutralize not only SARS-CoV-2 but a broad range of other coronaviruses as well.
If successfully translated to humans, the approach, published October 8, 2021, in the Journal of Experimental Medicine, could lead to the development of a next-generation vaccine capable of preventing future coronavirus pandemics.
The
SARS-CoV-2 virus responsible for COVID-19 enters
human cells by using its spike protein to bind to a cell surface receptor
called ACE2. The receptor-binding domain of the spike protein consists of two
parts: a “core” region that is very similar in all coronaviruses, and a more
specialized “head” region that mediates binding to ACE2.
Antibodies that recognize the head region of the spike receptor-binding domain can block the entry of SARS-CoV-2 into cells but offer little protection against other coronaviruses, such as the SARS-CoV-1 virus responsible for the severe acute respiratory syndrome outbreak of 2002.
Antibodies that recognize the core
region of the spike receptor-binding domain, in contrast, can prevent the entry
of various coronaviruses into human cells. Unfortunately, however, individuals
exposed to the viral spike protein tend to produce lots of antibodies against
the head region but few, if any, antibodies that recognize the core region.
“This suggests that, although the generation of broadly neutralizing antibodies is possible, SARS-CoV-2 infection and current vaccines are unlikely to provide protection against the emergence of novel SARS-related viruses,” explains Professor Tomohiro Kurosaki from the WPI Immunology Frontier Research Center at Osaka University in Japan. “Given that prior coronavirus epidemics such as SARS-CoV-1 and MERS-CoV have occurred due to zoonotic coronaviruses crossing the species barrier, the potential for the emergence of similar viruses in the future poses a significant threat to global public health, even in the face of effective vaccines for current viruses.”
Kurosaki
and colleagues decided to test a new vaccination strategy that might enable the
immune system to produce more broadly neutralizing antibodies. The researchers
genetically engineered the receptor-binding domain of the SARS-CoV-2 spike
protein, covering its head region in additional sugar molecules. These sugar
molecules could shield the head region from the immune system and boost the
production of antibodies against the unshielded core region of the
receptor-binding domain.
Indeed,
mice immunized with these engineered proteins produced a much higher proportion
of antibodies recognizing the core region of the spike protein receptor-binding
domain. These antibodies were able to neutralize the cellular entry of not only
SARS-CoV-2 but also SARS-CoV-1 and three SARS-like coronaviruses from bats and
pangolins.
Much
work will need to be done to translate this strategy to humans, but, says
Kurosaki, “our data suggest that engineered versions of the spike
receptor-binding domain could be a useful component for the development of
broadly protective, next-generation vaccines to prevent future coronavirus
pandemics.”
Reference:
“Glycan engineering of the SARS-CoV-2 receptor-binding domain elicits
cross-neutralizing antibodies for SARS-related viruses” 8 October 2021, Journal of Experimental Medicine.
DOI: 10.1084/jem.20211003