Soon, single universal jab to give lifelong protection against all flu strains

A single flu vaccine that would protect against all strains of the virus for life may be coming soon, which could make annual flu jabs that cost the NHS around 100m pound per year a history.

Scientists working on the universal flu jab, known as Flu-v, are in the early stages of development but hope to offer a product to the NHS within three to five years.

The company behind the drug, SEEK, will present the results of a small-scale clinical trial at the Influenza Congress in Washington DC on Tuesday.

Results so far have shown that it can significantly reduce infection rates and also cut the severity of symptoms.

Because flu is so changeable, pregnant women, the elderly and other ‘at risk’ groups are given a new injection every year.

The flu virus regularly mutates its `outer coat`, which is what a vaccine usually targets.

But the team behind Flu-v has managed to isolate a thread common to all strains of flu and by targeting that element, rather than the changing `outer coat`, the vaccine can cater for all requirements.

That means it would protect against strains of bird flu and swine flu, as well as seasonal variants.

`The trial suggest was only need one shot of vaccine,` the Daily Mail quoted Gregory Stoloff, the chief executive of SEEK as telling The Telegraph.Our aim is for the flu vaccine to become more like the mumps and measles – where you only need it once and you get protection for a long time,` he stated.

Source: http://food.sify.com

 


Sustained protection against cholera in humans up to five years.

The study showed the vaccine had a protective efficacy of 65 percent over a five-year period.

The landmark study was collaboration between scientists from the International Vaccine Institute (IVI) an international organization based in Seoul, and the National Institute of Cholera and Enteric Diseases, (NICED), an institute under the Indian Council of Medical Research (ICMR) of India’s Ministry of Health and Family Welfare.

Cholera is a potentially deadly infectious disease that causes profuse, dehydrating diarrhea in children and adults.

The oral cholera vaccine (OCV) contains strains of killed cholera bacteria that have been previously shown to be safe in humans and is administered through a two-dose regimen.

The vaccine was specifically developed for use in developing countries through a public-private partnership led by IVI with support from the Republic of Korea, Sweden, and the Bill and Melinda Gates Foundation.

The partnership involved Shantha Biotechnics (part of the Sanofi group) based in Hyderabad, India; VaBiotech, a state-owned vaccine manufacturer located in Hanoi, Vietnam; and the University of Gothenburg in Sweden.

The vaccine, which is produced by Shantha Biotechnics in India and licensed as Shanchol, was prequalified by theWorld Health Organization (WHO) in September 2011.

“The study results suggest that this vaccine will protect persons at risk of severe cholera for five years,” Dr. Thomas F. Wierzba, Deputy Director General of Vaccine Development and Delivery at IVI and co-author of the study, said.
“With protection sustained for five years, we will be able to provide greater benefits to the poor at reduced costs,” he said.

The study is published in the Lancet Infectious Diseases.
Source: http://www.newstrackindia.com


New Ebola treatment may offer hope for cure

Canadian researchers said Wednesday they have developed an antibody treatment that may be able to prevent death from Ebola virus even when given three full days after infection.

The findings, published in the U.S. journal Science Translational Medicine, suggested that it may be possible to develop a cure for Ebola even after the virus can be detected in the blood and disease symptoms have become apparent.

Although rare, Ebola virus is considered one of the most if not the most aggressive virus known to date in part because of its rapidity to kill, which can be within one week from exposure or three to four days from when the first symptoms become apparent. This leaves very little time for any treatment to act and save a sick individual.

“For this reason, such a treatment has been considered by many to be closer to the domain of science fiction than contemporary scientific research,” lead author Qiu Xiangguo at the Public Health Agency of Canada told Xinhua.

In their study, the researchers gave Ebola-infected monkeys a treatment made of three specific antibodies in combination with interferon alpha, a molecule that is produced naturally by the body to fight viruses.

The antibodies are “like three little but powerful missiles” that target three different outer regions of the virus, Qiu said. Once in contact with the virus external coat, these antibodies interfere with the virus lifecycle and reduce the ability of the virus to reproduce. At the same time, the interferon alpha boosts the defenses of the infected individual by stimulating a natural but rapid and robust anti-viral response, she said.

The combination of antibody and interferon therapy was 75 percent and 100 percent protective in cynomolgus and rhesus monkeys when given three days post-infection. About half of the cynomolgus monkeys were protected at four days post-infection in cases where only interferon alpha was given earlier, one day post- infection, Qiu said.

“Although we were very optimistic we were not expecting to see 100 percent survival in Ebola-infected non-human primates when treated only three days before they succumb to the disease on average,” Qiu said.

“This study shows that what seemed impossible to many, i.e. to develop a cure capable of stopping Ebola virus on its track only a few days before death, has now been made and proven efficacious in conditions that are at least as serious if not more severe than what has been observed and described in humans,” she added.

The researchers said they have tentatively scheduled a phase I safety trial, slated for the end of 2014 or early 2015, to test the combination therapy in humans

Source: http://news.xinhuanet.com


Cats may be key to HIV vaccine

There have been numerous studies showing how dogs can benefit human health, by sniffing out cancer, for example. Now it is time for cats to shine, as researchers say they may hold the key to a human immunodeficiency virus (HIV) vaccine.

Researchers from the University of Florida and the University of California, San Francisco, have discovered that blood from patients infected with HIV shows an immune response against a feline AIDS virus protein.

Janet Yamamoto, professor of retroviral immunology at the College of Veterinary Medicine at the University of Florida and corresponding study author, told Medical News Today:

“Since FIV (feline immunodeficiency virus) and HIV-1 are distant cousins and their sequences are similar, we used the T cells from HIV positive human subjects to see if they can react and induce anti-HIV activity to small regions of FIV protein, which lead to the current story.”

The team’s findings are published in the Journal of Virology.

New vaccine-development strategy for HIV

The researchers say they are working on a T cell-based HIV vaccine that is able to activate an immune response in T cells from individuals against the feline acquired immunodeficiency syndrome (AIDS) virus.

T peptides are small pieces of protein that are crucial in this process, as they trigger the body’s T cells to distinguish viral peptides on infected cells and attack them.

However, Prof. Yamamoto says that not all HIV peptides are able to work as vaccine components. Some enhance HIV infection or have no effect, while others have anti-HIV activities that become lost if the virus changes or mutates to avoid immunity.

Previous studies have shown that when combining various whole HIV proteins to create vaccine components, the results have not been strong enough to create a commercial vaccine.

But the researchers believe that the feline AIDS virus could be used to discover areas of the human AIDS virus, and this could lead to a new vaccine-development strategy for HIV.

“We had difficulty in identifying ways to select regions on HIV-1 for HIV-1 vaccine. Our work shows how to select the viral regions for HIV-1 vaccine. The regions on FIV or their counterpart on HIV-1 that have anti-HIV T cell activities can be used as a component for human HIV-1 vaccine,” says Prof. Yamamoto.

FIV triggers T cells to kill HIV

To reach their findings, they acquired the T cells of patients who were infected with HIV. The T cells were isolated and incubated with different peptides that the researchers say are crucial for survival of both the human and feline AIDS viruses.

On comparing the reactions of the feline immunodeficiency virus (FIV) peptides with the reactions of the HIV peptides, the researchers discovered one particular peptide region on FIV that triggered patients’ T cells to kill HIV.

They found that the feline viral region by human cells seems to be “evolutionarily conserved.” This means it is present in many viruses similar to AIDS across animal species.

This feline viral region must be crucial, the researchers note, as it is unable to mutate in order for the virus to survive.

Prof. Yamamoto notes that so far, there have been no T cell-based vaccines used to prevent any viral diseases:

Dr. Jay A. Levy, professor of medicine at the University of California, San Francisco, and study author, stresses that their findings do not mean that the feline AIDS virus infects humans.

“Rather,” he adds, “the cat virus resembles the human virus sufficiently so that this cross-reaction can be observed.”

Prof. Yamamoto told Medical News Today that more of these cross-reactive regions on FIV need to be observed, as well as regions on the monkey AIDS virus

Source: http://www.medicalnewstoday.com/articles/266911.php


FDA approves first pre-surgical breast cancer drug

Federal health officials say they have approved a biotech drug from Roche as the first medicine labeled for the treatment of breast cancer before surgery.

The Food and Drug Administration approved Perjeta for women with a form of early-stage breast cancer who face a high risk of having their cancer spread to other parts of the body.

Surgery to remove tumors is usually the first step in treating most forms of cancer. Perjeta is the first drug to be approved as a pre-surgical step.

The FDA gave the drug accelerated approval based on a study showing women who received the drug as an initial treatment were more likely to be cancer-free 12 weeks later than women who received older drug combinations.

Source: Fox news


Vitamin D-based treatment key to halting Multiple Sclerosis

Researchers have discovered a vitamin D-based treatment that can halt – and even reverse – the course of the disease in a mouse model of Multiple Sclerosis (MS).

The treatment involves giving mice that exhibit MS symptoms a single dose of calcitriol, the active hormone form of vitamin D, followed by ongoing vitamin D supplements through the diet.

Lead scientist biochemistry professor Colleen Hayes said that all of the animals just got better and better, and the longer we watched them, the more neurological function they regained.

While scientists don’t fully understand what triggers MS, some studies have linked low levels of vitamin D with a higher risk of developing the disease. Hayes has been studying this “vitamin D hypothesis” for the past 25 years with the long-term goal of uncovering novel preventive measures and treatments.

Over the years, she and her researchers have revealed some of the molecular mechanisms involved in vitamin D’s protective actions, and also explained how vitamin D interactions with estrogen may influence MS disease risk and progression in women.

First, Hayes’ team compared the effectiveness of a single dose of calcitriol to that of a comparable dose of a glucocorticoid, a drug now administered to MS patients who experience a bad neurological episode. Calcitriol came out ahead, inducing a nine-day remission in 92 percent of mice on average, versus a six-day remission in 58 percent for mice that received glucocorticoid.

Next, Hayes’ team tried a weekly dose of calcitriol. They found that a weekly dose reversed the disease and sustained remission indefinitely.

But calcitriol can carry some strong side effects – it’s a “biological sledgehammer” that can raise blood calcium levels in people, Hayes says – so she tried a third regimen: a single dose of calcitriol, followed by ongoing vitamin D supplements in the diet.

The study has been published online in the Journal of Neuro immunology.

Source: http://article.wn.com

 


Vaccine ‘clears HIV-like virus’ in monkeys

The researchers now want to move from monkeys to test the vaccine in humans

A vaccine for the monkey equivalent of HIV appears to eradicate the virus, a study suggests.

Research published in the journal Nature has shown that vaccinated monkeys can clear Simian Immunodeficiency Virus (SIV) infection from their bodies.

It was effective in nine of the 16 monkeys that were inoculated.

The US scientists say they now want to use a similar approach to test a vaccine for HIV in humans.

Prof Louis Picker, from the Vaccine and Gene Therapy Institute at Oregon Health and Science University, said: “It’s always tough to claim eradication – there could always be a cell which we didn’t analyse that has the virus in it. But for the most part, with very stringent criteria… there was no virus left in the body of these monkeys.”

Search and destroy

The research team looked at an aggressive form of virus called SIVmac239, which is up to 100 times more deadly than HIV.

Infected monkeys usually die within two years, but in some inoculated primates the virus did not take hold.

It maintains an armed force that patrols all the tissues of the body, all the time, indefinitely”

Prof Louis Picker Oregon Health and Science University

The vaccine is based on another virus called cytomegalovirus (CMV), which belongs to the herpes family.

It used the infectious power of CMV to sweep throughout the body. But instead of causing disease, it has been modified to spur the immune system into action to fight off the SIV molecules.

“It maintains an armed force, that patrols all the tissues of the body, all the time, indefinitely,” explained Prof Picker.

The researchers gave rhesus macaque monkeys the vaccine, and then exposed them to SIV.

They found that at first the infection began to establish and spread. But then the monkeys’ bodies started to respond, searching out and destroying all signs of the virus.

Of the monkeys that successfully responded to the vaccine, they were still clear of infection between one-and-a-half and three years later.

Prof Picker said his team was still trying to work out why the vaccination worked in only about half of the monkeys.

“It could be the fact that SIV is so pathogenic that this is the best you are ever going to get.

“There is a battle going on, and half the time the vaccine wins and half the time it doesn’t,” he said.

Human trials

The researchers are now testing the vaccine to see if it can be used after SIV exposure to treat and potentially cure infected monkeys.

They also want to see if the technique could work in humans.

Prof Picker said: “In order to make a human version we have to make sure it is absolutely safe.

“We have now engineered a CMV virus which generates the same immune response but has been attenuated [modified to lose its virulence] to the point where we think it is unequivocally safe.”

This would first have to pass through the regulatory authorities, but if it does, he said he hoped to start the first clinical trials in humans in the next two years.

Commenting on the research, Dr Andrew Freedman, from Cardiff University School of Medicine, said: “This suggests that prophylactic vaccines – vaccines designed to prevent infection – using CMV vectors may be a promising approach for HIV.

“While they may not prevent the initial infection, they might lead to subsequent clearance, rather than the establishment of chronic infection.”

Source: http://www.bbc.co.uk


Nanodiamonds boost treatment of chemo-resistant leukemia

By binding multiple molecules of a common leukemia drug with nanodiamonds, scientists have managed to boost the delivery of the drug to leukemic cells and retain the drug within the cells to combat the cancer.

This novel discovery, reported for the first time, addresses one of the major challenges in the treatment of leukemia where the cancer cells develop ways to pump drugs out of the body before they can do their job, particularly after they are exposed to chemotherapeutics.

Developed by Dr Edward Chow, Principal Investigator at the Cancer Science Institute of Singapore and Assistant Professor at the Department of Pharmacology, Yong Loo Lin School of Medicine at National University of Singapore (NUS), in collaboration with Professor Dean Ho of the UCLA School of Dentistry, this innovation shows promise for greater efficacy in treating leukemia, particularly in non-adherent cells.

Daunorubicin is currently one of the most common drugs used to treat leukemia. The drug works by slowing down or stopping cancer cells from growing, causing many of them to die. It is also common, however, for leukemia to become resistant to this drug after treatment.

One mechanism by which this opposition, commonly known as chemoresistance, happens is through the expression of drug transporter pumps in leukemia cells that actively pump out chemotherapeutics, including Daunorubicin.

Current approaches to neutralising chemo-resistance have centred on developing competitive inhibitors. These efforts have limited success, with challenges like high toxicity levels and less-than-promising results during clinical trials.

The team of scientists from NUS and UCLA turned to nanodiamonds, which are tiny, carbon-based particles that are 2 to 8 nanometers in diameter, as an option to address chemo-resistance.

Dr Chow studied the biological basis of how nanodiamonds can potentially overcome chemo-resistance.

The scientists bound the surfaces of nanodiamonds with Daunorubicin, and the hybrid nanodiamond-drug complexes were introduced to leukemic cells.

The research team found that nanodiamonds could carry the drug to the cancer cells without being pumped out.

Due to their non-invasive sizes and unique surface features, nanodiamonds can be easily released without blocking up blood vessels.

The findings are published online in the medical journal Nanomedicine: Nanotechnology, Biology, and Medicine.

Source: Zee News


Microbe Transplants Treat Diseases That Drugs Can’t Fix

Billie Iverson may be getting up there, but for an 86-year-old, she’s still plenty active.

“I take trips, and I go do my own shopping, and I take myself to the doctor,” Iverson says. “I do everything. I don’t let anything stop me.”

But one day, she got hit with something she’d never experienced — the worst case of the runs ever.

For days at a time, off and on for weeks, the problem kept coming back. Iverson eventually got so weak, she ended up in for days at a time, off and on for weeks, the problem kept coming back. Iverson eventually got so weak; she ended up in a nursing home.

“I just thought maybe I wasn’t going to make it,” she says. “I thought I was going to die.”

Finally, Iverson’s daughter took her to see Colleen Kelly, a doctor at Brown University. Kelly knew right away what was going on.

“It’s very classic, this pattern,” Kelly says. “We’ve seen hundreds of cases over the last couple of years at our program.”

Kelly’s program specializes in the microbes that live in our digestive systems — trillions of bacteria, viruses, fungi and other mostly helpful microbes whose genes scientists collectively call the human microbiome .

The problem, she told Iverson, started when antibiotics prescribed for another health problem disrupted the community of benign organisms in her intestines, leaving her vulnerable to a really bad bug — a bacterium called Clostridium Difficile

“You can almost look at C. diff as … the prototypical example,” Kelly says, of how a disruption in the human microbiome can result in disease.

Kelly is among a growing number of doctors who are starting to use what scientists are learning about our microbiomes to help prevent, diagnose, and treat many illnesses. For Iverson, she proposed something that may sound pretty radical — what doctors call a fecal transplant

“It’s really almost like an organ transplant,” Kelly says. “You’re taking this whole community of microorganisms from one person, [and] transplanting them into another person. Then these things … take root, colonize and kind of restore that balance.”

Iverson says she initially found the idea repulsive. But she felt so desperate that she agreed to try it.

“I was scared to death, honey,” Iverson says. “I’m an old lady. I’ve got one foot in the grave and the other on the banana peel.”

The procedure turned out to be really easy. And it worked — virtually overnight. “It stopped,” Iverson says. “Right away. I’m feeling good now. I’m feeling great.”

What happened to Iverson is the most dramatic example of how doctors are manipulating the microbiome in lots of ways to help lots of different kinds of patients.

For one thing, Kelly says doctors are testing the use of the transplants in other illnesses, such as colitis, Crohn’s disease and diabetes. And there’s even talk of trying the treatment for obesity.

“We’re at a really interesting point in medicine where we’ve come to appreciate the microbiome and that [these organisms] have really integral roles in … energy metabolism, and immune function, and all of these other things,” Kelly says.

At the same time, researchers are looking for more subtle ways to fix our microbiomes. For starters, they’re trying to remove the “yuk” factor from microbiome transplants by figuring out exactly which microorganisms patients really need and giving them just those. And there’s tons of research involving so-called probiotics — live cultures of supposedly beneficial microbes, typically included in yogurt or other foods or supplements probiotics are meant to be swallowed, in hopes that they’ll outcompete pathogenic bacteria and restore a healthy balance.

The evidence is really mounting to the point where I think it’s undeniable that the ingestion of live bacteria — safe bacteria in high numbers — has an overall beneficial effect on human health,” says colin hill of the University College Cork in Ireland.

Scientists are testing a long list of probiotics for a variety of health problems, including vaginal infections, colic in babies and weakened immune systems in the elderly. They’re also studying so-called prebiotics— non digestible carbohydrates meant as food for the good microbes.

Now, anyone who walks into a grocery store these days knows that hundreds of prebiotic and probiotic products are already on the market. You can’t watch TV or go on the Internet without hearing the kinds of claims the manufacturers of these products make.

The companies point to studies supporting their claims. But many experts say there are still huge questions about how safe such products are, how pure they are, and whether they really do what their makers say they do.

“All of those things together open up the opportunity for … the equivalent of snake oil salesmen related to probiotics or microbial treatments, or fecal transplants or whatever,” says Jonathan Eisen of the University of California, Davis.

And Eisen is not alone in his criticism. The Food and Drug Administration has big concerns. Those concerns include whether microbiome transplants might spread infections, or are being promoted for unproven uses, or whether they might actually increase the risk for some health problems.

“The gut microbiome can affect obesity, diabetes [and] a number of other disorders,” says Jay Slater, director of the FDA’s Division of Bacterial, Parasitic and Allergenic Products. “These are the kinds of concerns that would indicate that good long-term studies really should be done.”

So the FDA requires that doctors who want to do microbiome transplants for anything other than C-diff treatment get FDA approval first. And physicians must warn patients that, even for C-diff, the treatment is still experimental. Scientists studying probiotics have to put them through the same careful testing that regular drugs go through.

All this is really frustrating for many scientists. They argue that these regulatory roadblocks are holding up research and making it too hard for patients to get microbiome transplants.

“People are dying of C. diff,” says Kelly. “And people are living in this really terrible state. I see people who’ve lost their jobs, people who’ve become depressed because of just the feeling of utter hopelessness. And I think it’s really unethical to withhold the treatment from patients who need it.”

As for Iverson, she agrees that anyone who needs such a transplant should be able to get one.

“I think it’s terrific,” she says. “I think it’s the best thing that ever happened. This is like a step to heaven having this done.”


New method could help in early detection of colon cancer

Bettina Scholtka, said that tumour cells are released into stool from the surface of precancers and early-stage colon cancers

Scientists have found a new method to detect genetic variations that initiate colon cancer could be readily used for non-invasive colon cancer screening.

Bettina Scholtka, Ph.D., assistant professor in the Department of Nutritional Toxicology at the University of Potsdam in Nuthetal, Germany, said that tumour cells are released into stool from the surface of precancers and early-stage colon cancers, but detecting a cancer-initiating genetic mutation among a large quantity of normal DNA from a patient’s stool is like looking for a needle in a haystack.

Scholtka said that by combining for the first time locked nucleic acid-based, wild-type blocking polymerase chain reaction and high-resolution melting, we were able to achieve the desired sensitivity.

Scholtka and colleagues used 80 human colon tissue samples representing cancers and precancers to detect genetic variations using a combination of two techniques: The first technique — locked nucleic acid (LNA)-based, wild-type blocking (WTB) polymerase chain reaction — suppressed normal DNA present in large quantities in the sample; and the second technique — high-resolution melting (HRM) — enhanced the detection of genetic variations.

The researchers were able to detect APC variations in 41 of the 80 samples. They were also able to detect previously unknown variations in APC. In contrast, the routinely used technique called direct sequencing could detect variations only in 28 samples.

They then analyzed 22 stool samples from patients whose colon tissues had APC variations, and nine stool samples from patients whose colon tissues did not have APC variations, as controls. They were able to detect APC variations in 21 out of 22 samples.

The study has been published in Cancer Prevention Research.