Why your coronavirus vaccine will probably keep
working
For now, public health experts say, it’s not time to
panic.
PORTUGAL-VIRUS-HEALTH
People
queue for the vaccine in Lisbon, Portugal. Vaccines are the best defense, say
health officials, even against the Delta variant that is on the rise in
countries including Portugal and the UK | Patricia de Melo Moreira/AFP via
Getty Images
BY CARLO
MARTUSCELLI AND HELEN COLLIS
July 5,
2021 9:15 pm
https://www.politico.eu/article/why-your-vaccine-will-probably-keep-working-to-stop-the-coronavirus/
It’s a
nightmare scenario: A coronavirus variant escapes science’s cleverly
constructed defenses and returns to spreading unchecked, sending more than a
year’s work to develop and administer billions of vaccine doses up in smoke.
The most
recent cause for alarm is the highly infectious Delta variant, first identified
in India, which is pushing up case numbers again in countries like the U.K. and
Portugal, prompting some EU countries to issue a new round of travel
restrictions.
But for
now, public health experts say, it's not time to panic.
So far,
most argue, the chances of a runaway coronavirus mutation dodging the
protective effects of a vaccine — known as an escape variant — appear slim even
though some variants might swerve around immune defenses slightly. The main
driver for the most recent spike in infections in some countries is in fact not
a vaccine failure or an especially dangerous variant. It's the fact that they
had populations that have been only partially or not at all vaccinated — while
some governments rushed to relax lockdown restrictions before large majorities
were fully jabbed.
That’s not
to say that authorities should lower their guard. There’s some evidence that
vaccines are less effective against the South African variant. And as long as
the coronavirus is spreading in other places, like South Asia and South
America, the risk of a further proliferation of variants is real. Some of
those, known as variants of concern, appear to be more transmissible and have
been linked to a higher chance of hospitalization, with the Delta variant as
one example.
With so
much of the world still not vaccinated, the opportunities for further mutation
are a chief concern for David Heymann, professor of infectious disease
epidemiology at the London School of Hygiene & Tropical Medicine and
distinguished fellow at Chatham House.
Nonetheless,
"we're in good shape," he said. "With influenza, we have to wait
six months for a new vaccine" due to the time it takes to harvest the
active substance from chicken embryos. By contrast, mRNA vaccines can be
modified and produced in six weeks.
It's in
everyone's interest to ensure people acquire "a high level of
protection" from vaccines to avoid a worse-case scenario, he added,
warning that "right now that's not occurring."
So far so
good
With much
of Europe and the U.S. jabbed, the real-world data so far suggest the antibody
immunity given by vaccines appears to be holding up.
This
finding is a relief to scientists who had worried about the risk that, in
theory, the pressure created by the vaccine-induced antibody protection could
encourage particular mutations that allow the virus to sidestep vaccines. If
this process is repeated for a number of generations, a variant might emerge
that could totally avoid vaccine-induced immunity.
To be sure,
certain mutations of the spike protein — the part of the virus that latches
onto target cells — lower the ability of antibodies "to neutralize and
stop the virus from infecting cells," said Gary McLean, a professor in
molecular immunology at the London Metropolitan University.
But he
believes there's only so much a typical virus can change.
"It's
going to hit a wall at some point," McLean said, adding that the
coronavirus "may almost already be there."
In short,
there's a trade-off between how much the virus can change — and thereby
"escape" a vaccine's effect — and how effective it can be in
continuing to spread, he explained. Because current vaccines target the spike
protein of the coronavirus, this is where changes in the virus have to
concentrate. If the virus changes too much, it can no longer properly infect
cells.
"There's
going to be a point where the virus can't mutate anymore because it's done all
the mutating it can possibly do," he said.
Andreas
Radbruch, scientific director at the German Rheumatism Research Center and
president of the European Federation of Immunological Societies, also believes
it's "extremely unlikely that there will be an escape from the
vaccines."
So far,
Radbruch said, research suggests variants are concentrating mutations in just a
few locations on the virus' spike protein.
So while
variants may pose problems for individual monoclonal antibodies, it’s unlikely
that one "would escape the current vaccines," he explained. This is
because the body produces thousands of different antibodies that target
different parts of the spike protein.
In this
sense, it was lucky that the coronavirus has been comparatively
"conservative" so far, he said. Unlike the seasonal flu virus, it
cannot "come up with completely new spike proteins that don't have any
similarity to the existing one."
That said,
this feature poses a problem in another respect, specifically for monoclonal
antibodies — one of the most effective treatments for severe coronavirus
infections — because some target these individual parts of the spike protein.
In the U.S., a number of states have even paused distribution of Eli Lilly's
antibody treatment precisely for this reason.
Original
sin
Meanwhile,
how long the immunity granted by existing vaccines lasts is still an open
question.
While
researchers are looking into modifying the shots to better respond to
circulating variants, some say that second or third generation vaccines based
on different variants of the virus may not elicit as strong an immune response
as the first-generation jabs.
At issue is
what some call the "original antigenic sin" — the immune system's
tendency to mount a stronger defense against the first version of the antigen
it encounters — either through natural infection or vaccination. This reaction,
in turn, knocks out the immune system’s ability to mount as strong a defense
against mutated forms of that antigen. This phenomenon has been seen with the
seasonal flu and the ongoing problem that flu jabs — which are less effective
than COVID-19 vaccines — need to be modified annually.
"When
you get reinfected with a new strain, your antibodies are more likely to be
re-stimulated, to be provoked again to make more antibodies against the parts
of the protein that haven't changed,” explained Charles Bangham, professor of Immunology at Imperial College London.
So the
immune system mounts a strong response to the bits of the antigen it
recognizes, overshadowing the slower and weaker response to the mutated bits of
the antigen it hasn't encountered before.
However,
Bangham isn't concerned for now and sees this scenario more as a
"theoretical danger."
He notes
that antibodies can recognize many parts of the spike protein that haven't
mutated and therefore still can be effective.
Moreover,
it’s not only antibodies that are primed; T cells also play an important role
in fighting infections. "They recognize a lot of other parts of the spike
protein,” said Bangham. If someone is naturally infected with Delta, they will
also respond to other proteins in the virus, which tend to mutate less than the
spike protein.
"So
both antibodies and T cells are still active against not only the spike protein
but all the other proteins in the virus," he said.
In
Bangham’s view, the best way to avoid escape variants and mount a strong immune
response to the evolving virus would be to design a "polyvalent"
vaccine that contains parts of the Delta variant as well as Alpha and Beta
(first identified in the U.K., and South Africa, respectively). "That is
likely to cover a very high proportion of the infections" today and in the
future, he said.
England’s
Chief Medical Officer Chris Whitty agrees, noting that polyvalent vaccines
"will hold the line to a very large degree against even new variants"
within five years.
A fine line
For all the
advances in science, policymakers must now grapple with the complexities of a
partially vaccinated world.
In the
U.K., for example, after an initial sharp drop in new cases, infections have
started to increase rapidly again. The good news is that unlike during previous
waves of the virus, mortality appears to be barely budging, even taking into
account the lag between infections and deaths. Ministers decided in June to
delay a full reopening of the country, but on Monday Prime Minister Boris
Johnson announced plans to drop final restrictions on July 19, including mask
wearing, and urged the public to use their own "judgement."
Meanwhile,
other countries with relatively high vaccination rates are facing new
challenges. Some, like Poland and Romania, are dealing with a high degree of
vaccine skepticism. And even within the ranks of people who have received a
shot, some are immunocompromised or suffer from existing conditions like
diabetes that make them more vulnerable.
Danny
Altmann, professor of immunology at Imperial College London, sees this shift as
moving away from "black and white debates" during the height of the
pandemic when thousands were dying daily. Now, policymakers have to take a more
granular and nuanced view, particularly when it comes to deciding the right
level of protection to minimize avoidable deaths in vulnerable populations.
"The
more variants that come around the bend, the more evasive they are, the more
problems we might have with ... people who don't have good enough
immunity," he explained. "The question then becomes: What's my
tipping point when it becomes unacceptable, where I either need a vaccination
program with a modified vaccine, or I need more frequent boosters."
"The
debates are much more complex," he added. "But I don't think that I'm
going to have the same conversation with you in a year's time saying 'My god, that
Zeta variant took us by storm and conquered the world.'"

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