The Wall Street Journal - 04.04.2020 - 05.04.2020

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C2| Saturday/Sunday, April 4 - 5, 2020 **** THE WALL STREET JOURNAL.


It would
have
been
devilishly
difficult
to lock

down the


U.S.
earlier.

typical, Italy was seen at the
time: its demographics, the
high proportion of Chinese visi-
tors, the spotty availability of
health care.
What’smore,wouldithave
been feasible—politically, ad-
ministratively—to lock down
the U.S. sooner? How could we
have expected people to keep
children home from school,
stop working and suffer the
enormous economic losses we
are now seeing when the
threat was still seen by most
(including experts) as a low-
probability outcome?
All the time, we have to
make almost impossibly diffi-
cult estimates around the risk-
reward calculus of our actions.
Even now, as the virus threat is
unmistakable, some argue that
it does not justify the economic
devastation of the lockdown.
History suggests that we
rarely get these decisions right.
In the 1930s, Britain and France
failed to head off the threat
posed by Nazi Germany. In the
summer before Sept. 11, 2001,
the White House was warned of
an impending al Qaeda attack
and failed to head it off. These
were not failures of leadership.
They were almost inevitable
failures of human nature.
We never act until it’s too
late, mainly because most of
us don’t believe the threat is
real until it is. WILLIAM CAMPBELL-CORBIS/GETTY IMAGES

EDITOR
AT LARGE

GERARD
BAKER

thority—who have
decided to con-
tinue functioning
moreorlessas
normal.
I write this not
to join the orgy of
finger-pointing
that is now rou-
tine. Quite the op-
posite. For all the
name-calling and
blame-apportion-
ing we are now
doing, the evi-
dence of much of
history is that the
failure to respond adequately to
a looming threat is embedded
in our nature. Expecting us to
respond to an impending chal-
lenge by taking the most ex-
treme measures to prevent it is
expecting something we have
rarely done—something ahis-
toric and virtually unhuman.
Much of the media’s cover-
age of the past couple of weeks
has been built around validat-
ing the claim that the U.S.
failed to protect its people from
this extraordinary scourge and
is, as a result, headed for a far
more devastating outcome than
just about anywhere else on the
planet. The focus is, of course,
very much on the president.
Warnings were missed, it’s said,
and scientists ignored—all be-
cause of President Trump’s de-
termination to keep public con-

city’s hospitals.
Many in the same
media organiza-
tions now con-
demning the pres-
ident’s dilatory
response were
themselves dis-
missing Covid-19
as nothing worse
than a seasonal
flu. Neither will
we forget how
many of them denounced as xe-
nophobic one early measure
that the president did take to
protect the U.S.: the decision to
block flights from China in late
January.
The point is not that individ-
uals failed to respond ade-
quately. It’s that it is devilishly
difficult, especially in a com-
plex democracy, to mobilize a
community to preempt a chal-
lenge of this sort.
In hindsight, it was probably
epidemiologically optimal to
lock down the entire country a
month earlier than we did—in
mid- to late February, let’s say.
We should have known, some
say, because we had the experi-
ence of Italy. But look back at
the commentary on Italy a
month or so ago, and you will
see how particular, rather than

fidence high and the economy
strong ahead of the election.
It’s surely true that Mr.
Trump’s repeated dismissals of
the seriousness of the threat
contributed to a sense of secu-
rity in the early stages of the
epidemic that we now know
was misplaced. More could
have been done, especially to
ramp up testing capacity. But to
move from that proposition to
the argument that Mr. Trump’s
assurances were responsible for
blocking preventive action is a
leap at odds with all we know
about human behavior.
For one thing, the president
wasn’t alone. Those of us in
New York City will long re-
member Mayor Bill de Blasio
exhorting us to go out to bars
when there was already evi-
dence of extreme stress in the

Main Street in
Livingston, Mont.,
March 20.

THERE ARE SOME PLACESin
the U.S. where, as I write, you
can still go into a bar, order a
drink and have a meal within a
few feet of fellow diners. “Take
me there!” we may be tempted
to say, especially those of us
who are already weeks into a
mandatory lockdown diet of
home-cooked food, experimen-
tal cocktails and takeout.
These last, fading glimpses
of normality are still visible as,
everywhere, the scale of the
threat from Covid-19 has be-
come abundantly clear: thou-
sands of deaths already and
multiples more to come.
We have known for some
time now how much of a men-
ace this epidemic is and that
proximity among humans is the
primary means by which people
will get sick and die. Still, in
places there seem to be some—
citizens as well as those in au-

We Only


Ever Fight


Threats


When


They’re


Upon Us


REVIEW


tant model for the future.
In all of these efforts, an essential
balance must be struck between the
wish to quickly get remedies to se-
verely ill patients and the potential for
intolerable side effects. In addition,
media hype can lead to treating pa-
tients with ineffective medication in
the face of better choices. The experi-
ence with Covid-19 is a powerful re-
minder of the importance of conduct-
ing excellent clinical trials that
generate the proof needed to assure
caretakers and patients.
Anyone who studies the Covid-19
pandemic knows that we need a vac-
cine, and we need one
quickly. Yet, even more
than diagnostics and thera-
peutics, a safe and effective
vaccine will take time. Both
the pace and the breadth of
the efforts to produce a
vaccine are impressive. The
biotech company Moderna
wasthefirsttotreatapa-
tient with an experimental
vaccine only 66 days after
the viral sequence was
available. Today, WHO lists
dozens of vaccine ap-
proaches under study.
It is exciting to see how
advances in genomics,
structural biology and im-
munology have contributed
to more innovative ap-
proaches to vaccines. And
it is not only small compa-
nies who are participating.
Johnson & Johnson an-
nounced a collaboration
with the federal Biomedical
Advanced Research and De-
velopment Authority and a
commitment of $1 billion as well as
their manufacturing capacity. Global
collaborations for rapidly developing
and producing vaccines for Covid-19
include Biogen and VIR Biotechnology,
Pfizer and BioNTech, GlaxoSmithKline
and Clover Health, and many others.
Perhaps the key organization fo-
cusing on long-term preparedness is
the Coalition for Epidemic Prepared-
ness Innovations, funded jointly by
the Bill & Melinda Gates Foundation,
Wellcome Trust, the European Com-
mission and seven nations. Since 2017,
CEPI has been working to produce a
“plug and play” platform approach for
dealing with “Disease X,” a newly
emerging epidemic disease such as
Covid-19. The concept of a platform
technology would enable rapid vac-
cine development, elicit rapid onset of
immunity, and enable production to
be scaled up quickly to respond to
outbreaks.
This is the way forward—to focus
not only on the pathogens we know
but on preparing ourselves for the
pathogens we don’t expect. Today’s
epidemic is a powerful reminder that
infectious agents do not respect bor-
ders and that global cooperation is
essential for dealing with them. Clas-
sic public health tools are a must: We
cannot control what we cannot un-
derstand. And we need to maintain
the collaborative and generous spirit
that has emerged in response to
Covid-19. It may feel like a once in a
lifetime experience, but that, alas, is
unlikely to be the case. FROM TOP: DAVID L. RYAN/THE BOSTON GLOBE/GETTY IMAGES; MIKE SEGAR/REUTERS

anti-viral compounds, such as remde-
sivir, a compound developed by Gilead
Sciences, which failed in treatments
for Ebola but have shown promise
with some Covid-19 patients; antimi-
crobials, such as the antimalarial
drugs hydroxychloroquine and chloro-
quine, used together with the antibi-
otic azithromycin, which have shown
mixed results in small trials; and rem-
edies for severe Covid-19, such as the
compounds sarilumab from Regen-
eron Pharmaceuticals and Sanofi, and
toclizumab from Roche Holding. This
is just a small subset of medications
furthest along in their development.

The pursuit of therapies will be
further advanced by funding from the
newly launched Covid-19 Therapeutics
Accelerator (funded by the Bill & Me-
linda Gates Foundation, the Chan
Zuckerberg Initiative, Wellcome Trust
and Mastercard), specifically intended
to speed up R&D. There is also the
FDA’s Coronavirus Treatment Acceler-
ation Program, designed to fully staff
and support an accelerated regulatory
path for novel therapeutics. Many new
approaches to product development
are under way, using tactics ranging

from artificial intelligence to CRISPR
gene-editing.
An example of unprecedented col-
laboration is the QBI Coronavirus Re-
search Group, involving hundreds of
scientists at the University of Califor-
nia, San Francisco. These investiga-
tors have found 50 drug candidates
that shield proteins that the corona-
virus needs to thrive. It is an impor-

Scientific
innovation is
one of the
success
stories of the
response to
the Covid-19
crisis.

It is the role of the federal govern-
ment to adequately stockpile and plan
for a pandemic. Clear accountability
on the National Security Council,
matching the authority that already
exists for the military procurement
and supply chain, would allow asset
allocation to the states and regions in
greatest need. It would avoid what we
see today, with states competing
against each other for vital supplies.
Second, the concept of “surge ca-
pacity” does not appear to have been
part of the planning for ventilators,
and current needs massively exceed
normal demand. There is not only a
lack of supply but also a lack of readi-
ness—parts, established partnerships,
training—for quickly manufacturing
more machines. No single ventilator
company has significant excess capac-
ity, and none can produce large vol-
umes, so federal leadership is needed
to maximize the use of available ca-
pacity. There is also a clear need for
simpler ventilator designs, with stan-
dard parts to allow production to
scale up quickly.
The U.S. established the Strategic
National Stockpile in 2003 as an
emergency repository for antibiotics,
vaccines and other critical medical
supplies, but it has not adequately
served its role in this crisis. Covid-19
will focus attention on funding and
supplying it properly and planning for
distribution. For their part, the gover-
nors and mayors making
requests for aid today need
to be making “just in case”
plans for tomorrow, using
their experience with
Covid-19 to encourage the
reform and expansion of
the Strategic National
Stockpile.
Public Health.It is a
common complaint that
health systems and insur-
ers are too focused on ur-
gent and acute health
problems, treating disease
rather than investing in
prevention. We treat lung
cancer but underfund tobacco con-
trol, treat opioid addiction without
enough work on pain management,
and treat babies in intensive care
rather than give their mothers ade-
quate prenatal care.
This tendency to address what’s
right in front of us rather than pre-
venting what might happen in the fu-
ture is clear from the numbers. Ac-
cording to the Trust for America’s
Health, in 2017, public health repre-
sented just 2.5% of all U.S. health
spending ($274 per person). That
small portion covers prevention, pre-
paredness, wellness and community
recovery for all Americans. A pan-
demic takes full advantage of such un-
derinvestment, especially our failure
to make primary medical care widely
and easily available.
Good public health means that in-
dividuals are far less likely to be
struggling with hypertension, obesity
or diabetes. People who start out


Continued from the prior page healthier will experience lower rates
of morbidity and mortality when in-
fectious disease is spreading. Higher
vaccination rates are essential too,
since they mean that fewer people
will be sick with flu and other pre-
ventable infections and occupying
precious hospital beds.
Even more important, we must
have functional public health depart-
ments for essential disease-control
efforts like contact tracing
and quarantine. While our
global governance for
public health derives from
WHO, the national entity
we count on is the CDC
and ultimately state and
local public health depart-
ments.
These agencies have
been front and center for
our safety in the face of
multiple prior infectious
threats, from HIV/AIDS to
Ebola and Zika. This safety
is grounded in public
health basics. The essential
tool in an epidemic is in-
formation: who has the
disease and who have they
been in contact with?
Surveillance and epide-
miology are key tactics in
this quest, but critical gaps
in our capacity have been
clear since Covid-19 hit the
U.S. Of greatest impact


were the now well-known mistakes in
novel coronavirus testing that left the
government blind to its spread. This
inability to trace the pandemic was
exacerbated by the clinical manifesta-
tions of Covid-19. Current estimates
suggest that 25% of those infected do
not have symptoms. Failures in test-
ing and high rates of asymptomatic
patients meant that leaders, health-
care providers and decision makers
did not know the incidence or preva-
lence of Covid-19, which is the basic
information necessary to effectively
contain an epidemic.
Finally, public health must provide
expertise in an aspect so far lacking
in this pandemic: serologic surveil-
lance. This allows us to ask a second
key question: not whether individuals
currently have Covid-19 but whether
they were ever infected and are now
immune. The ability to do such test-
ing would allow us not just to under-
stand the biology and course of

The Steps Needed to


Avoid the Next Crisis


Covid-19 but also, potentially, to cer-
tify health caregivers and other
workers who will not risk acquiring
or transmitting the infection.
For future epidemics to be man-
aged more effectively, we must have
better information, and that means
having well-funded, well-trained and
well-prepared public health experts—
trained in statistics, epidemiology, and
laboratory and clinical medicine—at
the CDC and in the states
Innovation.Our ability to tap into
scientific innovation may turn out to
be one of the success stories in our
fight against the pandemic. Since

China released the SARS-
CoV-2 genetic sequence in
early January, countless
labs around the world have
been working to develop
new ways to test, treat and
prevent Covid-19.
On diagnostics and testing, scien-
tific innovation is not yet making a
difference. Serologic tests for antibod-
ies have lagged behind testing for the
disease itself, and despite multiple ac-
ademic and laboratory successes in vi-
ral detection, these advances have yet
to improve access to testing, accuracy
of results or speed of turnaround. Is-
sues have included inadequately
trained staff as well as the availability
of testing swabs and testing reagents.
Dealing with what might be consid-
ered the more mundane aspects of di-
agnostics is just as important as tech-
nical breakthroughs.
A true bright spot in innovation
has been the work happening on
treatment. Since the novel coronavi-
rus was reported in Wuhan, health-
care providers have been working to
repurpose existing medications. Bio-
tech and pharmaceutical companies
have fully participated in the early
tests. These have included work with

Lab work at Moderna,
which is testing
a Covid-19 vaccine
(above); N-95 masks at
a New York State
operations center (left).
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