lunes, 23 de marzo de 2020

COVID 19 - Japanese flu drug 'clearly effective' in treating coronavirus, says China

 
Patients given the medicine in Shenzhen turned negative in a median of four days 
Photograph: John Minchillo/AP

Japanese flu drug 'clearly effective' in treating coronavirus, says China
Shares in Fujifilm Toyama Chemical, which developed favipirav

Medical authorities in China have said a drug used in Japan to treat new strains of influenza appeared to be effective in coronavirus patients, Japanese media said on Wednesday.

Zhang Xinmin, an official at China’s science and technology ministry, said favipiravir, developed by a subsidiary of Fujifilm, had produced encouraging outcomes in clinical trials in Wuhan and Shenzhen involving 340 patients.

“It has a high degree of safety and is clearly effective in treatment,” Zhang told reporters on Tuesday.

Patients who were given the medicine in Shenzhen turned negative for the virus after a median of four days after becoming positive, compared with a median of 11 days for those who were not treated with the drug, public broadcaster NHK said.

In addition, X-rays confirmed improvements in lung condition in about 91% of the patients who were treated with favipiravir, compared to 62% or those without the drug.

Fujifilm Toyama Chemical, which developed the drug – also known as Avigan – in 2014, has declined to comment on the claims

Shares in the firm surged on Wednesday following Zhang’s comments, closing the morning up 14.7% at 5,207 yen, having briefly hit their daily limit high of 5,238 yen.

Doctors in Japan are using the same drug in clinical studies on coronavirus patients with mild to moderate symptoms, hoping it will prevent the virus from multiplying in patients.

But a Japanese health ministry source suggested the drug was not as effective in people with more severe symptoms. 

“We’ve given Avigan to 70 to 80 people, but it doesn’t seem to work that well when the virus has already multiplied,” the source told the Mainichi Shimbun.

The same limitations had been identified in studies involving coronavirus patients using a combination of the HIV antiretrovirals lopinavir and ritonavir, the source added.

In 2016, the Japanese government supplied favipiravir as an emergency aid to counter the Ebola virus outbreak in Guinea.

Favipiravir would need government approval for full-scale use on Covid-19 patients, since it was originally intended to treat flu.

A health official told the Mainichi the drug could be approved as early as May. 

“But if the results of clinical research are delayed, approval could also be delayed.”

Justin McCurry in Tokyo

jueves, 7 de febrero de 2019

Corn DNA: study how to design multi-resistant seeds


Stable yields, resistant to diseases and tolerant to higher temperatures are the requirements that must combine the cereal of the future.

Researchers study the regions of the genome and the mechanisms that are activated against pathogens or heat shock.

Originally from Central America and domesticated by man for the last 10,000 years, corn (Zea mays) is one of the three most cultivated cereals in the world that, thanks to its ability to adapt, managed to consolidate in production systems.

Used for both human, animal and biofuel production, among many other industrial uses, the global expansion of this crop is linked to the genetic improvement and development of varieties adapted to the needs of each place: today the cereal can be found from the warmest latitudes to the most temperate and from sea level to over 3,500 meters.

Sequenced in 2009 by an international team of scientists, it is now known that corn DNA is made up of 32,000 genes inserted into 10 chromosomes.

This finding confirmed the complexity of the cereal genome because 85% of its genomic sequences are repeated multiple times.

In other words, transposons - a genetic element that can move to different parts of the genome - jump around carrying part of the DNA that surrounds them, which generates mutations, increases genetic variability and makes DNA sequencing more difficult.

Because of this, his study was a great challenge.

Gerardo Cervigni is an expert in Genomics and works at the Conicet Center for Photosynthetic and Biochemical Studies, located in Rosario-Santa Fe.

There, he studies the structure, function and evolution of the genes that make up the DNA of corn. With the genome deciphered, Cervigni can map the genes, know how they work and predict the interactions that prevail.

"The exact location of the genes is essential to know their function," Cervigni said and said:

"With the map of corn, complete and orderly, and through the use of molecular markers, we can identify and associate the genes of resistance of a disease , plague or some characteristic of interest ".

Knowing exactly where the genes are will make it easier for plant breeders to create varieties that produce more grains, larger ones, or that are more tolerant of extreme heat or drought.


Corn DNA: study how to design multi-resistant seeds

The assisted improvement by molecular markers works directly with the DNA information.

This means that the researcher identifies which genes will provide the desired characteristics.

"This selection can be applied in the seedling stage, so the time to obtain better genotypes is reduced and the times and costs of the research are reduced considerably," Cervigni said.

Selecting the best characteristics and minimizing the likelihood that crops will be harmed by external factors are basically the objectives of classical genetics applied to vegetables.

"Knowing where are the genes that contain the characteristics of agricultural interest and how they work is very important for the future development of varieties," said Marcelo Ferrer, specialist in Genetic Resources of INTA.

According to Ferrer, the corn grown today is the result of a process of domestication, carried out by indigenous peoples of America, which consisted in selecting the best seeds and discarding the rest.

"In Argentina, there are more than 40 types of different varieties or local races of corn that are cultivated by farmers since ancestral times and that continue today in some regions of the north of the country, as in the Quebrada de Humahuaca," said Ferrer. He added:

"Adaptation to these climatic conditions was possible due to the great genetic richness of crops such as corn, potatoes and beans."

With the advance of technology and the incorporation of techniques for plant breeding it was possible to obtain crops adapted to the climate and soil conditions of a place.

However, to enrich the knowledge and possible agricultural improvements that can be incorporated, Ferrer stressed the importance of working with local materials as basic germplasm inputs both for breeding and for various basic genetic research for cultivation.

"Argentine materials grown more than 50 years ago, contained great genetic variability," Ferrer said, adding:

"At present, the most common - both in the core zone and in the rest of the country where large-scale maize is produced - is to find lots planted only with 'commercial hybrids' that are very productive, but they are very uniform and, in general, they are vulnerable since they resist or tolerate the attack of some plague or disease.

This is because they lost the variability that characterized their genome. "

Since 1950, the Germplasm Bank of INTA Pergamino has preserved seeds of more than 2,500 corn entries from all over the country.

"In addition to conserving the genetic resources of a country, the germplasm bank, through the characterization and evaluation works, allows us to identify materials that resist biotic and abiotic factors, which adapt to saline soils, at higher temperatures or in the absence of water ", exemplified Ferrer.


Ferrer: "The Argentine materials cultivated more than 50 years ago, contained a great genetic variability".

Super resistant corn

With a population that continues to increase, the need for increasingly efficient, yielding, stable and resistant to pests, diseases, as well as water stress -by excess or deficit- and thermal effects becomes imperative.

According to data from the United States Department of Agriculture (USDA), in 2017, world corn production reached 1031.86 million tons.

However, year after year, these values ​​are modified by various diseases that affect their productivity and the quality of the grains.

In this sense, a team of researchers from INTA Pergamino -Buenos Aires- seeks to identify in the maize genome which mechanisms are put in place against the attack of various pathogens.

Juliana Iglesias, a specialist in plant genetics at INTA and responsible for the study, uses genomic association tools to find gene regions of corn that are activated and allow the plant to resist multiple diseases.

Churches along with María Belén Kistner -bearer INTA-Conicet- aim to detect plants that possess the greatest genetic attributes to resist the most common diseases of economic interest.

"We focus on the search and identification of individuals that have genetic resistance to various diseases, in the future, to develop varieties that have better behavior to the attack of multiple pathogens,"

Iglesias said, adding: "We bet that it is a tool to reduce the use of phytosanitary products and contribute to their sustainable management ".


Iglesias: "We focus on the search for individuals that have genetic resistance to various diseases to develop varieties with better behavior against multiple pathogens."

According to Iglesias, the search for resistance to multiple diseases (MDR) is based on being able to find resistance hotspots (according to the academic term).

"Known as the genomic regions where genes accumulate for resistance to various diseases, the finding of hotspots, in addition to enabling the location of the gene or group of genes that are lit to resist diseases, will help us in the study of the mechanisms that are launched against the attack of various pathogens, "he explained.

"The groups of genes speak to us of patterns, of a relation between the pathogenic habits and the response of defense or susceptibility that the plant can give", analyzed Iglesias, who did a PhD in Cellular and Molecular Biology, at the University of Strasbourg, France.

Studies carried out in Pergamino -Buenos Aires- and in Leales -Tucumán- allowed us to identify which genotypes have the best behavior to pathogens and diseases.

Preliminary results showed that it is possible to group them according to their behavior against pathogens that have the same attack mode.

The pathogens can be biotrophs, hemiótrofos and necrotrophs, each one has different mechanisms to nourish, infect and produce symptoms.

In turn, the plants have different defense strategies that are put into operation according to the type of attack they receive.

"Diseases such as rusts, spike rot and blights generate certain defense responses that are due to the recognition of the pathogen that causes the attack," said the INTA biologist, adding:

"With these results, we can combine those genes, which are activated against similar mechanisms of attack and replicate its structure to obtain varieties with improved characters ".

"We studied the health response of approximately 100 inbred lines, which are part of the INTA Maize Improvement Program," Iglesias said.

The evaluation of foliar diseases in Parchment (rust, blight, bacteriosis, charcoal or charcoal of the spike) and in Loales (gray spot and blight), plus the information obtained on spike and grain rot (Fusarium and Aspergillus), allowed the team of researchers identify genotypes with resistance to more than one disease.

For Cervigni, this is an important finding in the general knowledge of the crop.

"We can establish an efficient protocol for phenotypic characterization and rapid selection of genotypes, whose genomes combine the desirable genes needed to obtain better results in the production of corn," he said.

Read the full story in spanish on the RIA Magazine site

INTA


lunes, 12 de febrero de 2018

Scientists Just Discovered Organisms That Are Distinct From Any Life Forms Known to Science



New Life

On the tree of life, humans share a branch with a diverse array of creatures, all with one thing in common: a backbone.

This single shared characteristic is enough to group us with dogs, fish, and lizards, in a group called a phylum; this is repeated throughout Earth’s organisms, connecting all of life’s diversity into one tree.

But now, researchers from University of Queensland (UQ) in Australia have uncovered an array of thousands of organisms so unique, they don’t fit into any existing phylum.

At the core of this research, which has been published in Nature Microbiology, was a relatively new technique known as metagenomics.

It involves the sequencing of all the DNA in a sample of an environment — dirt, water, feces, etc. — to produce that sample’s metagenome.}


A phylogenetic tree of life. Note how small the phylum Animalia — where humans fit in — is compared to bacteria and archaea. (Image Credit: Adl, Sina M.; Simpson, Alastair G. B.; et al.)

From an international database of more than 1,500 metagenomes, the UQ team reconstructed the individual genomes of 7,280 new bacteria and 623 new archaea.

Of these microorganisms, roughly a third were unlike anything scientists had seen before, warranting the creation of 17 new bacterial phylums and three new achaeal phylums.

“The real value of these genomes is that many are evolutionarily distinct from previously recovered genomes,” asserts lead researcher Gene Tyson.

“They increase the evolutionary diversity spanned by both bacterial and archaeal genome trees by over 30 percent, and are the first representatives within 17 bacterial and three archaeal phyla.”

Tiny Helpers

Microorganisms are notoriously difficult to study. Scientists have only been able to successfully culture one to two percent of all known bacteria and archaea in the lab, so analyzing them in their natural conditions through metagenomics may be the only way to study the rest.

However, while they may be tiny, these microbes can still have a huge impact on our world.

Right now, antibiotic resistance is a global problem of epic proportions.

Microbes have figured out how to adapt to the antibiotics we currently prescribe to treat health problems, and this resistance has killed as many as 23,000 people each year in the U.S. alone.

New forms of antibiotics are almost exclusively discovered in bacteria and fungi, so the species uncovered by the UQ researchers could eventually be developed into better antibiotics that are effective against these “superbugs.”



Past research has also identified unique industrial and environmental uses for microbes.

They’ve been used to create fertilizers for agriculture, and the ethanol produced by some can be found in dyes, detergents, and other products.

Scientists from the U.K. noted that newly evolved ocean microbes could be eating the vast majority of the plastic currently polluting our waters, and bacteria that live off of carbon could help in the battle against climate change.

Beyond the many potential uses for these newly identified organisms, their mere discovery is exciting for what it can tell us about the world we share.

As UQ researcher Donovan Parks told New Scientist, “All the questions we have about ancient evolutionary events — what our last common ancestor looked like, when methane metabolism arose, when oxygen-producing organisms evolved — they really benefit from having more genomes to look at and a more detailed tree.”

by Kristin Houser
futurism.com


sábado, 4 de febrero de 2017

DARPA’s Biotech Chief Says 2017 Will “Blow Our Minds”


The Luke arm is the most advanced prosthetic in world. 
Credit: John B. Carnett Getty Images

The Pentagon's research division is betting its high-risk, high-reward programs will change medicine

The Pentagon’s research and development division, DARPA—the creative force behind the internet and GPS—retooled itself three years ago to create a new office dedicated to unraveling biology’s engineering secrets.

The new Biological Technologies Office (BTO) has a mission to “harness the power of biological systems” and design new defense technology.

Over the past year, with a budget of about $296 million, it has been exploring challenges including memory improvement, human–machine symbiosis and speeding up disease detection and response.

DARPA, or the Defense Advanced Research Projects Agency, is hoping for some big returns.

The director of its BTO, neuroprosthetic researcher Justin Sanchez, recently spoke with Scientific American about what to expect from his office in 2017, including work on neural implants to aid healthy people in their everyday lives and other advances that he says will “change the game” in medicine.

[An edited transcript of the interview follows.]

Before your office was created in April 2014, DARPA had already worked on some biological projects—including research on combatting antibiotic resistance and mental health interventions. What’s changed with the creation of your office?

We had been doing biological work—at the interface of biology and engineering—for many years, but it was scattered throughout the offices.

With our office there was a recognition that biological technologies were going to play such a crucial role in not only shaping where our country was going, but the threats coming to our country, and we needed a focused comprehensive effort going forward.

I’m particularly intrigued by BTO’s hope to develop programmable microbes to produce needed medications on the fly—an effort to sidestep concerns about stockpiling the right drugs or worrying about complex transport logistics. That sounds amazing. Where is that work now?

That’s a program called “Living Foundries”—like a foundry where we would build something that’s alive.

Traditionally we use chemistry to make new compounds or new drugs.

But recently we’ve realized that microbes like yeast and bacteria can also produce compounds, and we can program them to make those compounds by first understanding the chemical pathways they use.

Take yeast. Yeast uses sugar for a variety of pathways to produce alcohols.

If you reprogram those pathways, however, you could potentially have yeast build a variety of different compounds that they weren’t initially designed to make and we would still use the same feedstocks—like sugar.

Our teams design the genetic codes that would be needed to reprogram the yeast.

That is such a different idea about how to revolutionize the way we build compounds.

That program set out to produce 1,000 new molecules throughout the duration of the program [which has three years left], and the teams are well on their way.

I believe they have produced close to 100 new compounds already using these new pathways in yeast.

It’s about thinking about biology and marrying it with engineering tools, and then using those two components to design something.

So you are in the early days of building compounds to spec?

Yes. They are on milligram quantities of these new compounds, but ultimately, throughout the course of the program, they are scaling up to kilograms.

If we can design these entirely different foundries for building these compounds, we think it could revolutionize how we think about drug development and also nonmedical approaches, because this is a platform technology.

Depending on what compound you are interested in—maybe some for medical uses or some that are for building a new material, like something more robust than the elements—there are lots of possibilities.

How will the new president-elect and Republican-dominated Congress affect your work?

We usually don’t get in the middle of those kinds of things.

The thing that I always like to emphasize is that our mission at DARPA remains the same no matter what the political climate is.

Our mission is about breakthrough technologies for national security.

It’s our job and role to think well ahead of what others in the world are thinking about for science and technology.

I think that mission transcends the vast political landscape that is out there.

We have a very focused mission and we are trying to keep our country safe…, so we are sticking to that mission no matter what happens, not only in this election cycle but in future election cycles.

What project at BTO are you most excited about for 2017?

It’s like your kids—you can’t have just one favorite.

I have multiple favorites. Let me share a few that will be really important to address in 2017.

The first is an area we call “Outpacing Infectious Disease.”

Our current approach, whenever a new pathogen hits our shores, is that everybody scrambles.

We want to get ahead of any pathogen that may hit our shores and be as ambitious as we can to take pandemics off the table.

We have pioneered new work in DNA and RNA approaches to immunization. Specifically, we are thinking about nucleic acid approaches to immunization.

The idea is that you can tell your cells that produce antibodies what the right code is for producing the antibodies that would be effective against a pathogen.

So you would get a shot, but that shot would have a code in it to tell your cells how to respond to that pathogen—and what that would lead to is a near-instantaneous immunity against that pathogen and an ability to really fight against it.

If you contrast that against the traditional way we think about infectious disease, where it takes months—if not years—to not only identify the pathogen but go through a long manufacturing process to produce vaccines with big bioreactors and so on, [the current] process is far too slow for the kinds of threats that are ultimately coming to our country.

That’s why we took this radically different approach to develop this fundamental technology, to have DNA- and RNA-based approaches to fight infectious disease.

I’m hoping we will have some big announcements about that in 2017.

What sort of announcements?

We are already getting some really good results in mouse models indicating that the nucleic acid approaches are working well.

We’re starting down the road of doing some safety work in humans.

Those are the early research steps.

We have every intention in the coming year of building new programs for this end-to-end platform.

We look forward to making some announcements about how we are working in this space in 2017 that show that this isn’t just an aspiration—this is something we’re going after in BTO.

If we are successful here,

I think it will change the game about how we think about infectious disease.

In the past few years there has also been a lot of buzz around brain-controlled prosthetics and exoskeletons. How does DARPA’s BTO fit into that space?

We are heavily vested in this area.

We just had a small ceremony at Walter Reed—we delivered the first two commercially available “Luke” prosthetic arms, the world’s most advanced prosthetic limbs.

We work so hard [on research], but to see it going to the veterans—that’s really great.

While that’s a step in brain-controlled prosthetics, we don’t stop there.

I think in the future there are a wide variety of devices that can be controlled via neural activity, not just the assisted kind but also a kind able-bodied individuals could ultimately use in their everyday lives.

Another thing we aspire to do in 2017 is think about neural technology in everyday life.

Really? What sort of applications are you thinking about for healthy, noninjured people to use in everyday applications?

I’m really intrigued by using neural technology to change how we interact with each other, how we communicate with each other and even maybe make decisions.

I’m thinking about cognitive assistance.

There are a whole host of ideas about how it could help a wide variety of people.

The door is just opening up to even think about these kinds of concepts, and to think about technology today to go down that road.

DARPA has often operated without a lot of public exposure about its projects, at least until the work is completed. How do you see that model fitting in with the reality that a lot of the medical work your office does would potentially affect or benefit American civilians writ large?

At DARPA we love sharing [our] vision with the world, and we like working extremely hard and diligently below the radar to make sure we are delivering upon our promises—and when things are right, we share them with the world.

One of the areas that we have been very out in the media about is our work on the Brain Initiative.

That was an area where Pres.

Obama set the challenge for our country. For the last couple years we have been working not only to prove out technology there [within the Brain Initiative], but also working with other federal agencies—NIH (National Institutes of Health) and NSF (National Science Foundation) to name a few—and to share our results internationally, so that other scientists and medical professionals could use the information that is coming out to accelerate ultimately what they are doing.

The other area that we have been very out in the open about publicly is our infectious disease work.

With every major milestone of testing a DNA or RNA approach we’ve made an announcement, and if one of the people we are funding gets additional funding from outside sources, we make an announcement.

Recently a DARPA-funded study, published in the journal Neuron, concluded that deep-brain stimulation failed to improve memory—and in fact actually worsened memory. But a previous study, a few years ago, found the opposite: that stimulation helped memory. So what does this mean for your office’s work in this area?

Neurotechnology is a very big area in our office.

We have made great strides on the medical side of things, showing direct neural interfaces

[connections between the brain and a device like a neurostimulator, computer or prosthetic] can restore movement, sensation and health with neuropsychiatric disorders.

What’s interesting, with respect to the study that just came out, is that a large portion of people think you can locate an important area of the brain and stimulate away, and magically we get a response!

That’s not the case.

When you map out what’s going on in the brain, we’ve found that if you don’t send the right codes into the brain you don’t get a facilitation of memory—and you can even impair memory.

The flip story is that if you do send the right codes in, you can get huge improvements in declarative memory.

The program has also seen that side of the work turn out.

So when I take a step back from seeing all of this and do an assessment of it, we have both sides of the coin.

We understand the codes that impair memory and facilitate memory.

I think it prompts deeper investigation for the next generation of brain exploration.

Just quickly, can you clarify what you mean by “code”?

The code is a couple of things. It is the precise firing of individual neurons.

Let’s say you have 100 neurons and they all fire at different times in different locations—it’s interpreting all that turning-off and turning-on when trying to remember the word “Nancy” or “tree”—we can understand what those firing patterns mean and how they relate to the outside world.

All those neural firing patterns collectively produce brain waves or rhythms, and we are studying the brain at that level, too.

It’s important to understand all those different facets of the brain because that’s how it works.

Without the ability to go in and make these measurements we would never have this understanding.

That’s why it’s so important that an organization like DARPA can go forward and develop neurotechnology to do this.

We have some teams on the program that are seeing huge improvements on memory performance in humans when you use the right kinds of codes.

Your office also has a “biochronicity” program that explores the role of time in biological functions and tries to manage the effects of time on human physiology.


We leave so much to chance because of our lack of understanding of biology.

I think our understanding of biology is vastly growing.

And our ability to interact with biology using engineering techniques will change the way we think about our body, brain and immune system—and the way we think about and interact with our food supply and things like that.

I see such exciting times moving into the future.

I think we are really hitting our stride now, and I think the kind of things and developments we will see in 2017 will really blow our minds.

By Dina Fine Maron

scientificamerican



CRISPR gene-editing tested in a person for the first time


Gene-editing could improve the ability of immune cells to attack cancer.
Steve Gschmeissner/Science Photo Library

The move by Chinese scientists could spark a biomedical duel between China and the United States.

David Cyranoski

A Chinese group has become the first to inject a person with cells that contain genes edited using the revolutionary CRISPR–Cas9 technique.

On 28 October, a team led by oncologist Lu You at Sichuan University in Chengdu delivered the modified cells into a patient with aggressive lung cancer as part of a clinical trial at the West China Hospital, also in Chengdu.

Earlier clinical trials using cells edited with a different technique have excited clinicians.

The introduction of CRISPR, which is simpler and more efficient than other techniques, will probably accelerate the race to get gene-edited cells into the clinic across the world, says Carl June, who specializes in immunotherapy at the University of Pennsylvania in Philadelphia and led one of the earlier studies.

"I think this is going to trigger ‘Sputnik 2.0’, a biomedical duel on progress between China and the United States, which is important since competition usually improves the end product,” he says.

June is the scientific adviser for a planned US trial that will use CRISPR to target three genes in participants’ cells, with the goal of treating various cancers.

He expects the trial to start in early 2017.

And in March 2017, a group at Peking University in Beijing hopes to start three clinical trials using CRISPR against bladder, prostate and renal-cell cancers.

Those trials do not yet have approval or funding.

Protein target

Lu’s trial received ethical approval from a hospital review board in July.

Injections into participants were supposed to begin in August but the date was pushed back,

Lu says, because culturing and amplifying the cells took longer than expected and then the team ran into China’s October holidays.

The researchers removed immune cells from the recipient’s blood and then disabled a gene in them using CRISPR–Cas9, which combines a DNA-cutting enzyme with a molecular guide that can be programmed to tell the enzyme precisely where to cut.

The disabled gene codes for the protein PD-1, which normally puts the brakes on a cell’s immune response: cancers take advantage of that function to proliferate.

Lu’s team then cultured the edited cells, increasing their number, and injected them back into the patient, who has metastatic non-small-cell lung cancer.

The hope is that, without PD-1, the edited cells will attack and defeat the cancer.

Safety first

Lu says that the treatment went smoothly, and that the participant will get a second injection, but declined to give details because of patient confidentiality.

The team plans to treat a total of ten people, who will each receive either two, three or four injections.

It is primarily a safety trial, and participants will be monitored for six months to determine whether the injections are causing serious adverse effects.

Lu’s team will also watch them beyond that time to see if they seem to be benefiting from the treatment.

Other oncologists are excited about CRISPR’s entry onto the cancer scene. “The technology to be able to do this is incredible,” says Naiyer Rizvi of Columbia University Medical Center in New York City. Antonio Russo of Palermo University in Italy notes that antibodies that neutralize PD-1 have successfully put lung cancer in check, boding well for a CRISPR-enabled attack on the protein.

“It’s an exciting strategy,” he says. “The rationale is strong.”

But Rizvi questions whether this particular trial will succeed.

The process of extracting, genetically modifying and multiplying cells is “a huge undertaking and not very scalable”, he says.

“Unless it shows a large gain in efficacy, it will be hard to justify moving forward.

” He doubts it will be superior to the use of antibodies, which can be expanded to unlimited quantities in the clinic.

Lu says that this question is being evaluated in the trial, but that it’s too early to say which approach is better.

nature.com



domingo, 3 de julio de 2016

Real Leather Without the Cow



Cow ears are perking up everywhere at the news that Brooklyn-based startup company Modern Meadow just received another round of funding.

The company is working on sustainable leather materials that have no need for cows or any other animal.

This is no plastic-based "pleather." Nuh-uh.

This material is cultured from living cells that produce collagen and proteins that create a "hide" that's biologically identical to leather made from cow skin.

Modern Meadow has a nice explanation here about how they do it.

But essentially, they edit DNA to instruct cells to manufacture certain types and quantities of proteins -- namely collagen, which gives skin its structure.

Next, they put the edited DNA into cells and let them multiply.

Like little factories with instructions to manufacture parts, the cells crank out the necessary proteins.

The collagen proteins group together into fibers, which themselves group together to ultimately form the hide.

From the material, designers can create garment, gloves, purses, shoes, belts, sofas or any other product normally made from leather.

All this without the toxic process of tanning a hide.

Chief Creative Officer for Modern Meadow, Suzanne Lee, told Tech Crunch that the processes can be tweaked to vary the leather's flexibility, elasticity, thinness or thickness -- depending on the customer's wishes.

The company just received $40 million in funding to scale up the process beyond research and development.

Modern Meadow is falling in line behind other companies such as Memphis Meats working to produce lab-grown meat products.

Moving the farm to the lab could, for the first time, make meat and leather sustainable products.

Because these days, meat and leather are the opposite of sustainable.

The industry wreaks havoc on the planet.

It produces abundant greenhouse gases, including methane and nitrous oxide, which are far more potent than carbon dioxide.

It requires large swaths of land, water, grain, and forces billions of animals to lives of suffering.

I haven't even mentioned the drugs.

Excessive use of antibiotics on industrial-scale farms is leading to the growth of superbugs in humans for which there is no treatment.

Scaling up lab-grown meat or leather will take some time, but this kind of innovation is just what the planet needs.

seeker.com

miércoles, 20 de marzo de 2013

Harvard's Wyss Institute and Sony DADC Announce Collaboration on Organs-on-Chips


Lung-on-a-chip
The Wyss Institute's lung-on-a-chip, made using human lung and blood vessel cells, is a device about the size of a memory stick that acts much like a lung in a human body. A vacuum re-creates the way the lungs physically expand and contract during breathing. [Credit: Wyss Institute]
Today the Wyss Institute for Biologically Inspired Engineering at Harvard University and Sony DADC announced a collaboration that will harness Sony DADC's global manufacturing expertise to further advance the Institute's Organs-on-Chips technologies.
Human Organs-on-Chips are composed of a clear, flexible polymer about the size of a computer memory stick, and contain hollow microfluidic channels lined by living human cells -- allowing researchers to recapitulate the physiological and mechanical functions of the organs, and to observe what happens in real time. 
The goal is to provide more predictive and useful measures of the efficacy and safety of new drugs in humans -- and at a fraction of the time and costs associated with traditional animal testing.
"We are excited to apply Sony DADC's deep manufacturing expertise to confront one of the major challenges in the life sciences by helping to accelerate the translation of the Wyss Institute's Organ-on-Chips from the benchtop to the marketplace," said Christoph Mauracher, Senior Vice President of the BioSciences division of Sony DADC. "The Organs-on-Chips have the potential to revolutionize testing of drugs, chemicals, toxins and cosmetics."
This collaboration builds on the momentum the Wyss Institute team has gained recently on its Organs-on-Chips research program. With support from Defense Advanced Research Projects Agency (DARPA)*, National Institutes of Health (NIH), Food and Drug Administration (FDA), and pharmaceutical partners, more than ten Organs-on-Chips are currently under development at the Wyss Institute, including a lung, heart, liver, kidney, bone marrow, and gut-on-a-chip; there is also a major effort to integrate these organ chips into "human body on-chips" that mimic whole body physiology.
In February, Wyss Founding Director Don Ingber, M.D., Ph.D., who leads the Organs-on-Chips research program, received the prestigious 3Rs Prize from the UK's National Centre for the Replacement, Refinement and Reduction of Animals in Research for the lung-on-a-chip. This month, the Society of Toxicology awarded him the Leading Edge in Basic Science Award for his "seminal scientific contributions and advances to understanding fundamental mechanisms of toxicity."
"Our work with Sony is a wonderful example of the Wyss Institute model in action," said Ingber. "We collaborate with industry to help de-risk the technologies we develop, both technically and commercially, and therefore expedite their translation into real world applications."
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*Part of this research was sponsored by the U.S. Army Research Office (ARO) and DARPA; the views and conclusions contained in this document are those of the authors and should not be interpreted as representing the official policies, either expressed or implied, of ARO, DARPA or the U.S. Government.

Contacts

Wyss Institute for Biologically Inspired Engineering 
Kristen M. Kusek
+1 617-432-8266
Kristen.kusek@wyss.harvard.edu 

Sony DADC
Manfred Koranda
+43 6246 880 8143
manfred.koranda@sonydadc.com
wyss.harvard.edu