Administering the MMR (measles, mumps, rubella) vaccine could serve
as a preventive measure to dampen septic inflammation associated with
COVID-19 infection, say a team of experts in this week’s mBio, a
journal of the American Society for Microbiology. Long-time
collaborators and spouses Dr. Paul Fidel, Jr., Department Chair, Oral
and Craniofacial Biology, and Associate Dean for Research, Louisiana
State University Health School of Dentistry and Dr. Mairi Noverr
Professor of Microbiology & Immunology at Tulane University School
of Medicine in New Orleans co-authored the perspective article based on
ideas stemming from research in their labs. Vaccination with MMR in
immunocompetent individuals has no contraindications and may be
especially effective for health care workers who can easily be exposed
to COVID-19, say the researchers.
“Live attenuated vaccines seemingly have some nonspecific benefits as
well as immunity to the target pathogen. A clinical trial with MMR in
high-risk populations may provide a low-risk-high-reward preventive
measure in saving lives during the COVID-19 pandemic,” said Dr. Fidel.
“While we are conducting the clinical trials, I don’t think it’s going
to hurt anybody to have an MMR vaccine that would protect against the
measles, mumps, and rubella with this potential added benefit of helping
against COVID-19.”
Mounting evidence demonstrates that live attenuated vaccines provide
nonspecific protection against lethal infections unrelated to the target
pathogen of the vaccine by inducing trained nonspecific innate immune
cells for improved host responses against subsequent infections. Live
attenuated vaccines induce nonspecific effects representing “trained
innate immunity” by training leukocyte (immune system cells) precursors
in the bone marrow to function more effectively against broader
infectious insults.
In Dr. Noverr’s laboratory, in collaboration with Dr. Fidel,
vaccination with a live attenuated fungal strain-induced trained innate
protection against lethal polymicrobial sepsis. The protection was
mediated by long-lived myeloid-derived suppressor cells (MDSCs)
previously reported inhibiting septic inflammation and mortality in
several experimental models. The researchers say that an MMR vaccine
should be able to induce MDSCs that can inhibit or reduce the severe
lung inflammation/sepsis associated with COVID-19. Mortality in COVID-19
cases is strongly associated with progressive lung inflammation and
eventual sepsis.
Recent events provide support for the researchers’ hypothesis. The
milder symptoms seen in the 955 sailors on the U.S.S Roosevelt who
tested positive for COVID-19 (only one hospitalization) may have been a
consequence of the fact that the MMR vaccinations are given to all U.S.
Navy recruits. In addition, epidemiological data suggest a correlation
between people in geographical locations who routinely receive the MMR
vaccine and reduced COVID-19 death rates. COVID-19 has not had a big
impact on children, and the researchers hypothesize that one reason
children are protected against viral infections that induce sepsis is
their more recent and more frequent exposures to live attenuated
vaccines that can also induce the trained suppressive MDSCs that limit
inflammation and sepsis.
The researchers propose a clinical trial to test whether the MMR
vaccine can protect against COVID-19, but in the meantime, they suggest
that all adults, especially health care workers and individuals in
nursing homes get the MMR vaccine. “If adults got the MMR as a child
they likely still have some level of antibodies against measles, mumps,
and rubella, but probably not the myeloid-derived suppressor cells,”
said Dr. Fidel. “While the MDSCs are long-lived, they are not life-long
cells. So, a booster MMR would enhance the antibodies to measles, mumps,
and rubella and reinitiate the MDSCs. We would hope that the MDSCs
induced by the MMR would have a fairly good life-span to get through the
critical time of the pandemic.”
Dr. Noverr was recently awarded a “Fast Grant” (part of Emergent
Ventures at the Mercatus Center, George Mason University) to test the
efficacy of MMR directly in a nonhuman primate model of COVID-19
infection.
https://www.eurekalert.org/pub_releases/2020-06/asfm-mvc061620.php
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