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Image Credit: Agencies

DUBAI: What if no virus emerged from Wuhan? And it's all just a nightmare we could now wake up from?

What if we already have a vaccine, at least one that works — i.e. safe and effective? Amidst this crippling pandemic that left millions homelocked for months, it's like a long bad dream we all wish we could wake up from.

Posing such “what if” scenarios can't be helped: What if the virus was contained in Wuhan from Day 1? Or Day 7?

It’s water under the bridge now, of course. The virus has spread far and wide, infecting 26.1 million people and killing about 864,000 as of September 3.

Proposed what-if scenarios:

1. What if no virus emerged from Wuhan, China?

After months of quarantines and economic meltdown, it would be a fabulous morning to wake up from this 2020 nightmare.

  • If someone were to tell the world the virus was just a bad dream — or fake news — there’s nothing like it.
  • There would be no billions of people being housebound for months.
  • No mental, physical and financial toll on people of all age groups in all corners of the world.
  • No extended period of a spontaneous and widespread shutdowns or reduction of business. No massive job losses and repatriation of jobless expat workers.
  • No devastation wrought on the health and wealth of the world, the full extent of which we’ve not seen yet.
  • We’d still be flying — with no masks on.
  • The biggest party of earth this year, the Dubai Expo 2020, would still be on.
  • The stock markets would have gone through the roof. Elon Musk would be quillionaire by now (overtaking Jeff Bezos), Bill Gates won’t be going around (on Webex) promoting vaccines.
  • And Zoom would still be irrelevant. Its founder Eric Yuan (age 50), won’t be worth $4 billion yet.
200131 dead wuhan
EDITORS NOTE: Graphic content / TOPSHOT - This photo taken on January 30, 2020 shows officials in protective suits checking on an elderly man wearing a facemask who collapsed and died on a street near a hospital in Wuhan. AFP journalists saw the body on January 30, not long before an emergency vehicle arrived carrying police and medical staff in full-body protective suits. The World Health Organization declared a global emergency over the new coronavirus, as China reported on January 31 the death toll had climbed to 213 with nearly 10,000 infections. - TO GO WITH China-health-virus-death,SCENE by Leo RAMIREZ and Sebastien RICCI / AFP / Hector RETAMAL / TO GO WITH China-health-virus-death,SCENE by Leo RAMIREZ and Sebastien RICCI Image Credit: AFP

2. What if, after the coronavirus emerged in Wuhan, containment measures were immediately put in place?

Go back to Scene #1.

It would have meant:

  • The whistleblower doctors were not silenced (5 Wuhan specialists went missing, and one died of the virus after exposing its true horrors).
  • Instead, they would have been paid close attention to. It would have meant the local communist party officials in the city were much smarter, and less of a thuggy-bully against the doctors.
  • It would have meant all of Wuhan and the rest of the world wouldn’t have had to deal with crushing effects of present contagion.
A selfie taken by Dr Li Wenliang,
A selfie taken by Dr Li Wenliang, 34, lying on a hospital bed this week wearing an oxygen respirator and holding up his Chinese identification card was shared widely online. Image Credit: Social Media

3: What if, when the virus first emerged, flights to and from Wuhan were grounded?

Perhaps the same as scene #1, with some slight differences.

NAT WUHAN AIRPORT-1580297191802
In this Tuesday, Jan. 21, 2020 photo released by China’s Xinhua News Agency, a staff member watches a screen showing temperature scans of passengers at Wuhan Tianhe International Airport in Wuhan in southern China’s Hubei Province. The number of cases of a new virus has risen to 440 in China and the death toll has risen to 9, Chinese health authorities said Wednesday. (Xiao Yijiu/Xinhua via AP) Image Credit: AP

4: What if scientists were able to develop a vaccine for SARS-CoV-1 (in 2003-05) and MERS (2015)?

It’s possible, with cross-reactivity in vaccines (against the same family of coronaviruses) kicking in, it may also work against SARS-CoV-2, based on the cross-reactivity found in memory T-cells of SARS-CoV-1 suvivors.

5: What if it takes too long for people to be convinced that a good COVID vaccine actually works?

The world does not need 100 different vaccines against one virus. That would be too confusing. the world needs more solidarity and collaborations

Narrowing down the time and selections would mean less waste, and a better chance to curb infections sooner.

6: What if vaccine trial subjects are kept to the maximum of 3,000 required, instead of 30,000 or 60,000 now being targetted by a number of vaccine makers?

3,000 is the number (maximum) required for Phase 3 drug trials, based on US Food and Drug Administration (FDA) guideliness.

Clinical trials guidelines documents FDA
Image Credit: Source: FDA [https://bit.ly/2EtWE6R]

7: What if, a COVID-19 vaccine is found effective in a much shorter time with 'human challenge trial' (HCT)?

  • The public benefit of such a trial for COVID-19 vaccine would still be massive.
  • One, at least a vaccine works, even if only for a certain segment of the population (i.e. young people).

8. What if a successful HCT would render other vaccine candidates obsolete?

No, not at all. A successful HCT for one vaccine does not necessarily spell doom for another.

The biggest challenge is what's faced each day by millions who deal with fear, hunger, death and economic dislocation as a result of further infections and lockdowns.

Sophie Rose (right) and Josh Morrison co-founded a group pushing a fast—and controversial—approach to COVID-19 vaccine trials and has volunteered to participate. The controversial ‘human challenge’ trials for COVID-19 vaccines 010202
Sophie Rose (right) and Josh Morrison co-founded a group pushing a fast—and controversial—approach to COVID-19 vaccine trials and has volunteered to participate. The controversial ‘human challenge’ trials for COVID-19 vaccines has gained support from 35,000 potential "subjects". Researchers say challenge studies would enroll between 15 and 150 participants and would likely yield definitive results in about six weeks. The planned 30,000-person Phase 3 vaccine efficacy trials, which do not involve deliberate infection, are likely to take six months, even on the accelerated timescale sought by Operation Warp Speed. Image Credit: @1DaySooner / Sophie Rose

9: What if the human challenge trial does fail and those young volunteers would be infected?

It's a valid question to ask. HCT is a controversial method because of how serious the disease can be -- and because its effects aren't fully understood.

There are ways to get around this dilemma. Scientists are reportedly now developing a less lethal coronavirus strain for human 'challenge' studies, the National Institute for Allergies and Infectious Diseases (NIAID) said in a statement on August 15, 2020.

In normal clinical trials, volunteers receive either a medicine or a placebo and their health is then followed over the course of months, or years. Scientists look for how well the vaccine or treatment worked when the person was naturally exposed to the pathogen. If one no, or only a few get exposed, the trial's results would be in doubt.

Vaccines that used the human challenge trials include shots for:

  • Malaria
  • Influenza
  • Typhoid
  • Dengue fever
  • Cholera
US phase three vaccine trials
A quicker way to test whether a drug works is by deliberately infecting volunteers, as has been done in the past for influenza, malaria, typhoid, dengue fever, and cholera.

10. experts are also concerned about elderly people getting a vaccine that works for them?

It’s a valid concern. A recent article in The Lancet (August 11, 2020) reported that 11 of the 19 WHO advisors were concerned that results for younger volunteers in an HCT might not be a valid predictor of efficacy, especially on older people.

Here’s a logical question to ask: If those 11 WHO experts do not agree to a human challenge trial — only because of their concern over the elderly — then wouldn’t a decision be self-defeating for the world?

11: What if that decision ('no' to any type of HCT under any circumstances) means confining the entire world to the concerns of the 11 WHO experts?

It’s the view held by a number of some WHO experts. And it's a valid one. No professional bio-statistician worth his salt would fail to insist on getting the widest possible age groups across the widest possible population groups in a sampling or efficacy/safety study.

Yet it’s up to the individual member government to follow the WHO experts or not. It’s an ethical question.

Though one must also ask: how can the rest of the world trust the same group or institution that uncritically parroted the Chinese party narrative — don’t-worry-there’s no-human-to-human transmission, no-need-for-a-mask-just-give-it-to-medical-workers, and the virus-jumped-from-a-wet-market (a point proven to be false by China’s own scientists) — to guide the rest of humanity about ethics on a coronavirus solution?

Human Challenge Trials means deliberately expose participants to infection, in order to study diseases and test vaccines or treatments. On August 15, 2020, US scientists are developing a strain of the coronavirus that could be used to deliberately infect volunteers in the so-called "challenge studies.”

It is a controversial method of vaccine development, in part, because, it goes against the Hippocratic oath among medical doctors (don’t cause harm).

A key benefit of human challenge trials for a COVID-19 vaccine, if allowed, would be to speed up vaccine development by months or more but could also place study volunteers at a much greater risk. 35,000 people from 150 countries have signed up as HCT volunteers, through a sign-up group called “1daysooner”.

12: What if human-challenge trials (HCTs) were to be conducted now?

Many within the WHO support the idea, as they believe the potential benefits far outweigh the risks, in case an HCT trial fails.

Here’s one point: If a vaccine is found effective in younger people (following an HCT conducted only on younger population, who can better resist the virus if the trial vaccine does not work), that does not mean the validity of other vaccine candidates taking the standard, long-term large-scale trial route would be invalidated.

Here’s another point: Data from those large-scale clinical trials (with tens of thousands of subjects) would still be useful in extrapolating benefit-risk analysis for the larger population, including the elderly.

“There are a variety of uses of human challenge trials other than deriving estimates of vaccine effectiveness,” states the The Lancet article.

“Moreover, even if one or more vaccines was found to be efficacious only in healthy, younger populations via a human challenge trial, this would still be useful in conjunction with other vaccines — since more than one vaccine is likely to be necessary — and healthy-population vaccines will help in ensuring sufficient supplies of other vaccines for higher-risk populations.”

13: What if a trial, right now, confirms at least one vaccine works?

The biggest benefit, of course, is this: Lesser economic dislocation — and lesser deaths too.

COVID-19's transmission will be curbed, even if only among the younger population.

“Even if a vaccine is found to work only on younger people,” states the experts in The Lancet Infectious Disease.  “Such a vaccine would also be economically beneficial, through allowing a large group of people to return to the workforce.”

Several HCT benefits were also outlined in a WHO document published in October 2016 (by the Expert Committee on Biological Standardisation in Geneva).

“Animal models are often quite imprecise in reflecting human disease, and many infectious organisms against which a developer might wish to develop a vaccine are species-specific for humans.”

“Human challenge trials may be safely and ethically performed in some cases, if properly designed and conducted. Tremendous insight into the mode of action and the potential for benefit in the relevant species – humans – may be gained from challenge trials.”

- WHO Guidelines on Human Challenge Trials

The experts added: “Human challenge trials may be safely and ethically performed in some cases, if properly designed and conducted. Tremendous insight into the mode of action and the potential for benefit in the relevant species – humans – may be gained from challenge trials.”

“However, there are also limitations to what challenge trials may be able to ascertain because, like animal model challenge-protection studies, a human challenge trial represents a model system. Because there are often such significant limitations to animal models, the model system of the human challenge trial may significantly advance, streamline and/or accelerate vaccine development.”

In general, a clinical trial measures how healthy people respond to the efficacy and safety of a candidate vaccine, explained Prof. M. Teresa Valenzuela, in a paper published by the Sabin Vaccine Institute.
A trial, in order to be valid, should “randomiSed, double-blind, placebo-controlled”. In such a trial, considered the “gold standard”, this where one group of the study receives the candidate vaccine, while the other group receives the placebo as the “control” group.
Several methodological considerations are discussed: how to structure a null hypothesis, how to select the study population and the importance and methods of randomization to avoid biases.

Source: Sabin Vaccine Institute

14. What if the guidelines for good clinical practices (GCP) and “informed consent” based on human subject protection (HSP) standards being used in current vaccine development is outdated?

These two elements — good clinical practices (GCP) and human subject protection (HSP) — are critical requirements.

Ethical conduct in research involving human subjects is important. In the case of the FDA, the regulations for the conduct of clinical trials incorporating these two elements, and have been in effect since the 1970s.

This is exactly the point about how technology trumps up standards.

For example, one evidence of “informed consent” of a subject involved in a clinical trial study is a signed paper document. In the pre-cloud era, recruitment of human volunteers took ages. Before internet came, a signature on paper is the best proof. Today, not anymore.

15: What if recruitment of volunteers is cloud based?

That’s what’s happening now, though it’s not clearly outlined in any existing guidelines we’ve seen so far (we’d like to be proven wrong on this).

Today, instead of recruiters "pulling” the subjects, going door-to-door, the subjects are now “pushing” themselves, signing up, as people get used to downloading apps, and then signing up in droves.

- -

Today, instead of recruiters "pulling” the subjects, going door-to-door, the subjects are now “pushing” themselves, signing up, as people get used to downloading apps, and then signing up in droves.

It’s like how instant messaging, Youtube and Tiktok trumped up all traditional media.

Cloud-based recruitment method had been extensively used by most vaccine developers, significantly cutting the cost and time.

16: What if there are people willing to be subjected to a 'human challenge trial' (HCT), literally offering their bodies to be deliberately exposed to the coronavirus after they’ve been vaccinated?

That’s also what’s exactly happening now. Or what tens of thousands of people have asked scientists to do on them. Offer up their bodies for deliberate infection from coronavirus.

It's the vaccine trial recruitment process in the 20th century being turned on its head. Now, with cloud recruitment, a number of problems is faced by a 60s-70s trial recruiters’ mind:

  • a. It’s not as laborious as before (like asking people “would you like to volunteer to get an experimental vaccine?);
  • b. It’s not as time consuming (15,000 subject recruited in two weeks, and 31,000 in six weeks in the case of the trial in Abu Dhabi)
  • c. It’s as expensive (just have a signup page).

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17. What if insisting on 'informed consent' is right, but the definition of how it’s obtained is wrong?

The “1daysooner” movement is social media-driven HCT recruitment drive.

1daysooner is a group of people who signed up to offer themselves as guinea pigs for “human challenge" trials. Thousand already signed up for this simple, yet scary, idea: “Give me one of the candidate vaccines, then expose me to the virus.”

This way, the group believes, it would quickly narrow the field of promising vaccines and speed up development.

As of August 24, 2020, some 35,00 “human challenge” volunteers from 150 countries already signed up with 1daysooner.

16. What if the recruitment for the SARS-CoV-2 vaccine prevented the use of the internet, or the cloud?

If trials, vaccine development, and collaborations among scientist must be done manually, using snail mail or telegram to communicate — that would indeed by tyranny of present-day Luddites, no different from those who burn suspected 5G mobile phone towers.

What if announcements (to recruit volunteers) were only valid if they’re done over the radio or printed newspapers?

That’s the scenario during the vaccine developments at least until the 1980s. During the time of Dr Edward Jenner, who developed the smallpox vaccine in 1796 (the world's first), there was no radio (invented in 1886) and it was 50 years ahead of New York Times’ first print-run.

The year the word "vaccine" was first used, there were still no established trial protocols — just humanity's urge to heal the sick with the knowhow and resources available then. 

18. What if today's vaccine makers world were to go back to 1796?

Back then, there's no Tiktok or instant messaging. The village limited one’s world. Horse was the main engine to move things and people around. No one had a passport. It was more than 200 years before transcontinental flights (with first Boeing 747 rolled out in 1969).

Yet in 1796, the vaccine was proven to work — because it simply worked — on one badly afflicted boy, aged 8, whose then recovered.

Before the introduction of a smallpox vaccine in 1796, on average 7.6% (1-in-13) of all deaths were caused by smallpox. Following its introduction, there was marked decline in smallpox deaths. Today, no one hears about smallpox-triggered deaths. Now, the anti-vaxxers can conveniently deny the existence of smallpox.

If old ways are used to tackle new challenges (like the novel coronavirus), then, Houston, we have a problem.

19: What if this article was dictated on a phone, while the writer is having a nightmare?

Go back to scenario #1.

Would you sign up for a 'human challenge trial'? Write to readers@gulfnews.com

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