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Gene editing announcement draws much debate, ASU professor comments.
August 8, 2017

ASU Professor James Collins, part of government advisory panels on CRISPR technology, weighs in on latest experiment

Scientists have for the first time edited genes in human embryos to fix a disease-causing mutation, according to a paper published (ironically) in the journal Nature.

They used a new, cheap and radical tool that enables geneticists and researchers to edit genomes easily by removing, adding or altering sections of DNA.

The technology is known as CRISPRCRISPR stands for Clustered Regularly Interspaced Short Palindromic Repeats., and the fears — and there are many — are that it could be used for human enhancement. Think super soldiers, or parents who create super kids to ensure success in life. Or that it could be used to create designer organisms that wreak havoc in nature. Or that it could be used to wipe out all mosquitos, when science does not yet know what function mosquitos perform in the wider ecosystem.

Two government advisory panels came out with dueling recommendations in the past 12 months. James Collins, Virginia M. Ullman Professor of Natural History and the Environment in the School of Life SciencesThe School of Life Sciences is in the College of Liberal Arts and Sciences. at Arizona State University, sat on one of them.

Collins was co-chair of the National Academy of Sciences' Committee on Gene Drive Research in Non-human Organisms: Recommendations for Responsible Conduct, a panel of 16 experts who released a lengthy report called “Precaution and governance of emerging technologies” in June.

ASU Now sat down to discuss the development with Collins.

“It’s a fascinating step in the use of this new CRISPR technology in terms of gene editing, opening up the possibility of using it in a variety of circumstances, whether it’s non-human animals or human beings,” Collins said. “It’s a fascinating technology that’s raising a lot of questions.

“It was in December of 2016 that the National Academy of Sciences held a meeting of international experts to discuss the possibility of using CRISPR for editing human embryos. It was at that meeting that they adopted a motion that the technology should not be used for editing human embryos, at least at this time. At the same time that meeting was going on, there was a committee of the National Academy of Sciences working on just this issue: Should CRISPR and other gene-editing technologies be used for editing the human germline in particular?”

Question: Changes to the germline are hereditary, correct?

Answer: That’s correct. Changes to the germline would be hereditary. They would go from one generation to the next.

Q: The panel endorsed only alterations designed to prevent babies from acquiring genes known to cause “serious disease and disability” and only when there is no “reasonable alternative.”

A: Exactly. That committee, in their report, came out with that recommendation, which is actually contrary to the recommendation that came out in December 2016. So you had two different opinions on the table.

Q: So there’s no consensus on this?

A: No, certainly in the larger community there would be no consensus. The community would be divided in a number of different ways, with one extreme — “Don’t do any gene editing at all” — and the other would vary gene editing under conditions as were described in that quote — serious, possibly lethal, mutations — that could be corrected, and then it would be appropriate to think about using the gene-editing technology, and not using the editing if it was just a question of enhancement.

Then the question becomes what counts as enhancement and what doesn’t count as enhancement? How do you make that decision? So, no, there’s not a consensus at this point.

Q: Do you think the experiment cited in the Nature paper was a toe dip on a slippery slope?

A: What it is is one more step of modifying human beings. In this case it’s going to be modifying human embryos. As the National Academy of Sciences put it, they open up the door to doing this sort of work in just this sort of circumstances. It’s an ideal case in this regard, where you can just reach in and you have a mutation and major defect and the change can be made and the embryo will develop without the defect, if everything works OK. That’s just the case the National Academy was looking towards. So is it a slippery slope?

The question then becomes — as far as the National Academy is concerned — when are you in a condition such as this where there’s a straightforward need as far as the viability of the embryo is concerned as opposed to just enhancement. Then you’re back to the question of what constitutes enhancement, and who makes that decision. That’s not clear-cut. My recollection is that the National Academy report authors were not clear on that either.

Q: What if a child produced through gene editing were hobbled in some unforeseen way?

A: Presumably that is going to be the kind of possibility that would be taken under consideration before this sort of technology is approved ultimately for use in human beings in a clinical environment. This is an experimental environment at this point. ... It’s just in a laboratory.

The question that you pose — an untoward effect — is something that’s going to have to be taken into consideration by the group that ultimately would approve the first clinical trials with this sort of technology. That would be the sort of consideration that would come into play when any sort of clinical intervention is considered. There’s always a risk associated with it, and the question would be what counts as a tolerable risk?

Q: Clearly there’s a lot more discussion that needs to happen about this technology.

A: There’s a lot more discussion that’s going to have to happen on the side of the ethical, legal and social implications of this sort of work. There’s a lot more discussion that’s going to have to happen on the research side as well.

There’s still a good deal of research to take place in order to fine-tune this technology for the purposes of making this as precise as possible so that the risk is going to be minimized. Which is what you’d want to do with any technology.

Scott Seckel

Reporter , ASU Now

480-727-4502

 
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ASU Biodesign scientists develop improved, potentially safer Zika vaccine

ASU takes a major step forward in boosting Zika prevention efforts.
August 9, 2017

Tobacco plant-produced vaccine could also be less costly, targeted for developing world

The worldwide Zika threat first emerged in 2015, infecting millions as it swept across the Americas. It struck great fear in pregnant women, as babies born with severe brain birth defects quickly overburdened hospitals and public health care systems.

In response, there has been a flurry of heroic scientific efforts to stop Zika.  Whole governments, academic labs and pharmaceutical companies have raced to develop Zika vaccines ever since global health experts first realized the dangers wrought by the mosquito-borne virus.

Now, Arizona State University has taken a major step forward in boosting Zika prevention efforts.

ASU Biodesign Institute scientist Qiang “Shawn” Chen has led his research team to develop the world’s first plant-based Zika vaccine that could be more potent, safer and cheaper to produce than any other efforts to date. 

“Our vaccine offers improved safety and potentially lowers the production costs more than any other current alternative, and with equivalent effectiveness,” said Chen, a researcher in the Biodesign Center for Immunotherapy, Vaccines and Virotherapy and professor in the School of Life Sciences. “We are very excited about these results.”

Rapid response network

Several potential Zika vaccines have had promising results in early animal and human tests. Last year, the Food and Drug Administration approved the first human testing of a Zika vaccine candidate, and this summer, a $100 million U.S. government-led clinical trial is underway.

But currently, there are no licensed vaccines or therapeutics available to combat Zika.

Several dedicated ASU scientists heeded the call to action, wanting to use their special know-how to find a way to overcome the pandemic crisis.

First, ASU chemist Alexander Green, along with collaborators at Harvard, developed a more rapid and reliable Zika test, an achievement highlighted by Popular Science in its “Best of What’s New” of 2016.

Now, Chen may have come up with a better vaccine candidate based on a key Zika protein. Chen is a viral expert who has worked for the past decade on plant-based therapeutics and vaccines against West Nile virus and dengue fever, which come from the same Zika family, called flaviviruses.

He honed in on developing a vaccine against a part of a Zika viral protein, called DIII, that plays a key role for the virus to infect people. 

“All flaviviruses have the envelope protein on the outside part of the virus. It has three domains. The domain III has a unique stretch of DNA for the Zika virus, and we exploited this to generate a robust and protective immune response that is unique for Zika,” Chen said.  

They first grew the envelope protein in bacteria, then switched to prepare the DIII protein domain in tobacco plants.

After developing enough material for the new vaccine candidate, Chen’s team performed immunization experiments in mice, which induced antibody and cellular immune responses that have been shown to confer 100 percent protection against multiple Zika virus strains in a mouse challenge.

Producing plant-based vaccines, especially in tobacco plants, is old hat for ASU researchers like Chen. For more than a decade, they’ve been producing low-cost vaccines in plants to fight devastating infectious diseases in the developing world.

It’s the same approach ASU plant research pioneer Charles Arntzen used when he played a key role in developing ZMapp, the experimental treatment used during the Ebola outbreak.

Artntzen’s Biodesign colleagues, including Chen, Hugh Mason and Tsafrir Mor, have continued to pursue plant-based vaccines and therapeutics to combat West Nile virus, dengue fever, nerve agents and even cancer.

Effective but not foolproof

While Chen has been cheering on Zika vaccine progress from other researchers, in each case there can be side effects.

To date, other scientists have tested several kinds of vaccines on mice — including one made from DNA and another from an inactivated form of the virus. With just one dose, both vaccines prompted the creation of antibodies that shielded the animals from becoming infected when they were exposed to the virus.

Any heat-killed vaccine runs the risk of accidentally injecting a live version of the virus if there is an error made in the vaccine production protocol. This tragic scenario happened occasionally with the polio vaccine.

For the second research group, they used the complete Zika envelope protein for their vaccine. Since envelope protein domains I and II are similar to West Nile and dengue viruses, this can cause a dangerous cross-reactive immune response.

“When you make the full native envelope protein as the basis for a vaccine, it will induce antibodies against DI, DII and the DIII domains of the protein,” Chen explained. “Those who have been prior exposed to DI and DII of other members of the Zika virus family may be prone to developing very bad symptoms, or in some cases, fatalities for dengue.”

In fact, animal experiments have shown that prior exposure to dengue or West Nile virus makes the Zika infection and symptoms much worse, suggesting a similar risk for people who had prior exposure to dengue (especially in South America, where it is more common).

“If you have prior exposure to dengue, and then have Zika exposure, the Zika infection may be much worse, and for men, may increase the likelihood of sexual transmission,” Chen said.

Chen’s protein-based vaccine uses the smallest and most unique part of the Zika virus that can still elicit a potent and robust immune response.

“In our approach, we make what we call a pseudovirus. It’s a fake virus. The pseudovirus displays only the DIII part of the envelope protein on the surface. This is at least as potent as previous vaccine versions.”

And he is very confident that his DIII-based protein vaccine will be safer.

“We did a test to make sure that the vaccine produces a potent protective immune response, but also, that it does not produce antibodies that may be cross-reactive for dengue, West Nile, yellow fever or others,” Chen said.

Fast track to the clinic

During the height of the Zika pandemic, whole countries of women were told not to become pregnant, due to babies born with a severe brain defect called microcephaly, in which the head and brain don't develop properly.

There have also been vision and hearing defects and learning disabilities associated with less severe infections.

To make matters worse, in adults, a debilitating nervous system condition called Guillain-Barre syndrome has also been shown to be caused by Zika.

While the most severe wave of the Zika pandemic has ebbed, it won’t go away anytime soon, and a vaccine still offers the best hope.

Tens of millions more could still be infected in the Americas in the coming years (see WHO fact sheet).

The ASU scientists were able to mobilize quickly from idea to proof-of-concept because they could leverage funds from an NIAID grant and seed funds from the Biodesign Institute.  

These are all made possible by generous federal, state and public support, including sales tax generated from the longtime Arizona innovation booster, voter-approved Proposition 301.

“This is a great example of the brightest minds quickly coming together, with public support, to take on one of the most significant public health challenges of our time,” said Josh LaBaer, executive director of the Biodesign Institute.

“That’s the essence of Biodesign at its best, and we hope this important proof-of-principal of a Zika vaccine can be translated quickly into the clinic.”

With the successful proof-of-principle, Chen hopes to partner with the medical community to begin the first phase of a human clinical trial in the next two years.

“Above all, we have to ensure the utmost safety with any Zika vaccine, especially because the people who will need it most, pregnant women, have the most worries about their own health, and the health of the fetus,” Chen said. “This has to be 100 percent safe and effective.”

Along with Chen, the research team included Ming Yang, Huafang “Lily” Lai and Haiyan Sun.

The research was published in the online version of Scientific Reports - Nature.

 

Top photo: ASU Biodesign Institute scientist Qiang “Shawn” Chen has led his research team to develop the world’s first plant-based Zika vaccine that could be more potent, safer and cheaper to produce than any other efforts to date.  

Joe Caspermeyer

Managing editor , Biodesign Institute

480-258-8972