Insights may lead to better ways to protect older people
Brown University
In a new study published in the
journal JCI Insight,
Brown University researchers describe the cellular and molecular events that
explain why these groups have a higher risk of infection as well as of severe
side effects and death.
“This paper details a major
discovery in COVID-19,” said corresponding author Dr. Jack A. Elias, an
immunologist and dean of medicine and biological sciences at Brown. “It shows
that levels of a protein called chitinase 3-like-1 increase with age as well as
co-morbid diseases and infection. What’s more, chitinase 3-like-1 augments SARS
CoV-2 infection.”
The findings not only answer
important questions about key mechanisms of the complex SARS-CoV-2 virus, Elias
said, but also have direct implications for the development of therapeutics to
control the viral infection.
Elias is part of a National Institutes of Health-funded laboratory that focuses on the cell and molecular biology of lung injury and repair. Researchers in the lab, including lead study author Suchitra Kamle and co-author Chun Geun Lee, have recently focused on the biology of enzymes and enzyme-like molecules, called chitinases and chitinase-like proteins, respectively. Of particular interest is a chitinase-like protein referred to as chitinase 3-like-1, a molecule naturally found in blood.
“We’ve been studying this gene
family here at Brown for a while and we know that it has a large number of
biologic effects, as well as tremendously important roles in both health and
diseases,” said Lee, a professor (research) of molecular microbiology and
immunology.
Chitinase 3-like-1 is the
cornerstone of a critical pathway that is activated during injury and
inflammation. These researchers and others have shown that circulating levels
of chitinase 3-like-1 increase during infection, especially in diseases
characterized by inflammation and tissue alterations — like emphysema, asthma
and COPD, some the same co-morbid diseases that are risk factors for COVID-19.
Interestingly, Lee said, levels of
chitinase 3-like-1 have also been shown to increase during normal aging. In
fact, they have been reported to be the best predictor of all-cause mortality
in people in their 80s.
The researchers thought they might
be able to take some of the work they’ve already done with this gene family and
apply it to COVID-19, Elias said. They decided to examine the relationship
between chitinase 3-like-1 and the receptor ACE2, the spike protein to which
the SARS-CoV-2 binds to enter human cells.
In a series of studies, the
researchers compared the effects of chitinase 3-like-1 on ACE2 as well as on
other protease enzymes that metabolize the spike protein and contribute to
infection. They examined these interactions in the lungs of mice that were
genetically modified to have exaggerated levels of chitinase 3-like-1 as well
as mice deficient in chitinase 3-like-1. In the lab, Kamle led experiments that
examined the effects of chitinase 3-like-1 on human lung epithelial cells.
The researchers found that levels of
chitinase 3-like-1 increased with age, co-morbid diseases and infection. In
addition, they noted that chitinase 3-like-1 was a potent stimulator of the
receptor that SARS-CoV-2 uses to infect cells.
Spurred by this discovery, the
researchers developed a humanized monoclonal antibody called FRG that attacks a
particular region of chitinase 3-like-1 — a step that turned out to be
critical. They found that this “therapeutic” antibody, as well as another small
molecule, powerfully blocked the induction of the ACE2 receptor.
“So in that way, the virus cannot
enter into the host system,” said Kamle, a Brown investigator in molecular
microbiology and immunology as well as antibody engineering. “This means there
will be less infection in the presence of this therapeutic FRG antibody.”
These findings could pave the way
for the development of therapeutics to protect people from infection, Elias
said.
“You can imagine a scenario in which
someone who has been exposed to a person who has the virus is given the
antibody, which then acts like a prophylactic to prevent infection or make the
symptoms that the infection induces milder,” he said.
Elias described another potential
scenario in which the person who has the virus is given the antibody or the
small molecule, which halts the infection and effectively “cures” the illness.
“We show in this paper that if we
make antibodies or other small molecules that can inhibit chitinase 3-like-1,
they can be therapeutics to control viral infection,” Elias said.
The team is currently looking at how
these antibodies and small molecules react with different variants of the SARS
CoV-2 virus, including the infectious delta variant that has recently changed
the course of the pandemic.
In addition to Elias, Kamle and Lee,
other Brown faculty who contributed to this research included Bing Ma, Chuan
Hua He, Bedia Akosman, Yang Zhou, Chang Min Lee, Wafik S. El-Deiry, Kelsey
Huntington and Olin Liang.
This work was supported by COVID-19
Research Seed Grant from Brown University, as well as by National Institute of
Health grants U01 HL108638, PO1 HL114501,R01 HL115813 and RO1 AG053495, as well
as grant USAMRMCW81XWH-17-1-0196 from the U.S. Department of Defense.
