AIDS groups call for “renaissance” in vaccine hunt

(Reuters) – Scientists searching for the Holy Grail of a vaccine against the incurable AIDS virus say recent encouraging steps should now galvanize efforts to use limited funds in smarter ways to drive the field forward.

International AIDS vaccine advocates said recent studies showing first evidence of vaccine-induced protection in humans and evidence that drugs designed to treat AIDS can also be used for prevention were signs of a “renaissance” in the search.

“This is a pivotal moment in HIV vaccine research,” said Alan Bernstein, executive director of the Global HIV Vaccine Enterprise. “The last five years have been the richest period in HIV vaccine research since the epidemic began. The question… now is how do we build on these scientific advances?”

Bernstein, whose group published a report on the “road to prevention” ahead of a major international conference on AIDS starting in Vienna on Sunday, said cross-border and cross-discipline collaboration among scientists was crucial.

And at a time when a global economic recession is squeezing funding for the AIDS battle, trying to attract new minds and ideas would be as important as trying to bring in new money.

There are around 20 drugs on the market to treat HIV and prevention measures have been deployed to try to stop its spread, but no vaccine exists against the human immunodeficiency virus (HIV) that causes AIDS. Since the AIDS pandemic started in the early 1980s, almost 60 million people have been infected with HIV, many of them in Africa, and it has killed 25 million.

In September 2009, scientists reported their biggest success yet with an experimental vaccine that showed a modest effect and appeared to slow the rate of infection by about 30 percent in Thai volunteers. And earlier this month, U.S. researchers found antibodies that can protect against a wide range of AIDS viruses and said they may be able to use them to design a vaccine.

OPTIMISM

Microsoft founder and philanthropist Bill Gates, whose Gates Foundation spends a large portion of its $34 billion fund on fighting AIDS, says he is now “optimistic about an HIV vaccine” — despite having said in 2005 “I’ll eat my hat” if one were developed in the next decade.

“The scientific results we’ve seen with the antibodies…and the Thai trial…really point us toward what we need to do,” he told reporters at a briefing ahead of the Vienna conference.

Bernstein pointed to several ways to strengthen HIV vaccine research and development, including getting more clinical trials up and running to test new ideas in humans, and expanding trials to those countries where people are most at risk of HIV.

There is also a need to speed up data sharing from trials and focus resources on the most promising scientific areas.

“Despite their fundamental importance to HIV vaccine development, only three vaccine concepts and four clinical efficacy trials in humans have been completed in 27 years since the virus was first identified,” the Enterprise report said. “With little clinical efficacy data to draw upon, many questions critical to guiding new approaches…remain unanswered.”

Seth Berkley, director of International AIDS Vaccine Initiative (IAVI), said the recent advances showed that research funding over the past decade was paying off. But he warned that the global financial crisis had already led to a 10 percent fall in investment in HIV vaccine research and development.

“This is not the time to slow the effort,” he wrote in a commentary in the New England Journal of Medicine. He said creating an effective vaccine would need innovation from academia and the drug industry, long-term, stable funding and “contributions from the best and brightest young scientists.”

AIDS groups call for “renaissance” in vaccine hunt

VIENNA, July 18 (Reuters) – Scientists searching for the Holy Grail of a vaccine against the incurable AIDS virus say recent encouraging steps should now galvanise efforts to use limited funds in smarter ways to drive the field forward.

International AIDS vaccine advocates said recent studies showing first evidence of vaccine-induced protection in humans and evidence that drugs designed to treat AIDS can also be used for prevention were signs of a “renaissance” in the search.

“This is a pivotal moment in HIV vaccine research,” said Alan Bernstein, executive director of the Global HIV Vaccine Enterprise. “The last five years have been the richest period in HIV vaccine research since the epidemic began. The question… now is how do we build on these scientific advances?”

Bernstein, whose group published a report on the “road to prevention” ahead of a major international conference on AIDS starting in Vienna on Sunday, said cross-border and cross-discipline collaboration among scientists was crucial.

And at a time when a global economic recession is squeezing funding for the AIDS battle, trying to attract new minds and ideas would be as important as trying to bring in new money.

There are around 20 drugs on the market to treat HIV and prevention measures have been deployed to try to stop its spread, but no vaccine exists against the human immunodeficiency virus (HIV) that causes AIDS. Since the AIDS pandemic started in the early 1980s, almost 60 million people have been infected with HIV, many of them in Africa, and it has killed 25 million.

In September 2009, scientists reported their biggest success yet with an experimental vaccine that showed a modest effect and appeared to slow the rate of infection by about 30 percent in Thai volunteers. And earlier this month, U.S. researchers found antibodies that can protect against a wide range of AIDS viruses and said they may be able to use them to design a vaccine.

OPTIMISM

Microsoft founder and philanthropist Bill Gates, whose Gates Foundation spends a large portion of its $34 billion fund on fighting AIDS, says he is now “optimistic about an HIV vaccine” — despite having said in 2005 “I’ll eat my hat” if one were developed in the next decade.

“The scientific results we’ve seen with the antibodies…and the Thai trial…really point us towards what we need to do,” he told reporters at a briefing ahead of the Vienna conference.

Bernstein pointed to several ways to strengthen HIV vaccine research and development, including getting more clinical trials up and running to test new ideas in humans, and expanding trials to those countries where people are most at risk of HIV.

There is also a need to speed up data sharing from trials and focus resources on the most promising scientific areas.

“Despite their fundamental importance to HIV vaccine development, only three vaccine concepts and four clinical efficacy trials in humans have been completed in 27 years since the virus was first identified,” the Enterprise report said. “With little clinical efficacy data to draw upon, many questions critical to guiding new approaches…remain unanswered.”

Seth Berkley, director of International AIDS Vaccine Initiative (IAVI), said the recent advances showed that research funding over the past decade was paying off. But he warned that the global financial crisis had already led to a 10 percent fall in investment in HIV vaccine research and development.

“This is not the time to slow the effort,” he wrote in a commentary in the New England Journal of Medicine. He said creating an effective vaccine would need innovation from academia and the drug industry, long-term, stable funding and “contributions from the best and brightest young scientists”.

Experimental vaccine may delay bowel inflammation and colon cancer

Washington, March 25 (ANI): A new experimental vaccine could delay bowel inflammation and colon cancer, researchers at the University of Pittsburgh School of Medicine say.

Their findings have appeared in Cancer Prevention Research, a journal of the American Association for Cancer Research.

According to senior author Olivera Finn, professor and chair, Department of Immunology, Pitt School of Medicine, people with chronic inflammatory disorders such as IBD are at greater risk for developing cancer at the inflamed site. In other cases, genes that develop cancerous changes can trigger inflammation.

The vaccine made by her team is directed against an abnormal variant of a self-made cell protein called MUC1, which is altered and produced in excess in both IBD and colon cancer.

Dr. Finn said: “Our experiments indicate that boosting the immune response against this protein early in the disease can delay IBD development, control inflammation and thereby reduce the risk of future cancers.

“These findings suggest also that the early stages of chronic inflammation might be considered a premalignant condition.”

For the study, the scientists tested transgenic mice that spontaneously develop IBD and then progress to colitis-associated colon cancer, producing the human version of MUC1 in both disease states. It was seen that animals that received the vaccine showed the first signs of IBD significantly later than those in two control groups that did not get the vaccine.

Microscopic evaluation of the colon tissue demonstrated less inflammation in the vaccinated mice, and no indication of cancerous changes. Nearly half of the animals in each of the control groups had evidence of abnormal tissue, and two had colon cancer.

Dr. Finn said: “The MUC1 vaccine seems to change the local environment from one that promotes cancer development to one that inhibits it.

“Certain immune cells that we usually see in the inflamed colon aren”t present, and that could make the surroundings less friendly for potentially cancerous cells that also are directly targeted by the vaccine for destruction.” (ANI)

Experimental vaccine shows promise against chikungunya

London, March 5 (ANI): Scientists have developed an experimental vaccine for chikungunya virus and successfully tested it in monkeys.

The vaccine, developed by at the National Institute of Allergy and Infectious Diseases, the University of Texas Medical Branch at Galveston, Purdue University and Bioqual Inc, is composed of non-infectious “virus-like particles.”

Although coated with the same proteins that enable chikungunya to pass through cell membranes, the vaccine particles lack the proteins that chikungunya uses to replicate inside cells.

They look like chikungunya to the immune systems of rhesus macaques, however, which respond to exposure by generating antibodies that defend the monkeys from infection by the real virus.

“This vaccine did an excellent job of protecting the macaques from chikungunya,” said UTMB professor Stephen Higgs, one of the paper”s authors.

“That it worked so well in a primate model is good news — these macaques are quite similar to humans in their response to chikungunya, and we badly need to develop an effective human vaccine for this virus,” he added.

To create the virus-like particles used in the experimental vaccine, the researchers used genetic engineering techniques to produce the structural proteins that produce the spiky, roughly spherical exterior possessed by chikungunya viruses before they have entered a cell.

The proteins then assembled themselves into harmless balls that resembled particles of Sindbis virus — a relative of chikungunya and a fellow member of the alphavirus genus, which also includes a number of insect-borne viruses capable of causing dangerous encephalitis in humans.

Serum drawn from rhesus macaques injected with the virus-like particles contained substantial levels of antibodies that inactivated chikungunya virus. Two groups of macaques were then inoculated, either with virus-like particles or with a sham solution containing no vaccine.

When the researchers challenged the monkeys by injection with chikungunya 15 weeks later, they found that the vaccine had completely protected the animals from the virus.

The research has been described in the March issue of Nature Medicine. (ANI)

Delivering vaccine through the skin may prevent ear infections in future

Washington, May 22 (ANI): Scientists at the Research Institute at Nationwide Children’s Hospital in Columbus, Ohio, say that an experimental vaccine that can be delivered through the skin has shown some promise to protect against certain types of ear infections.

The researchers reported their findings at the 109th General Meeting of the American Society for Microbiology in Philadelphia.

“Our data are the first to show that transcutaneous immunization is an effective way to prevent experimental ear infections and lays the foundation for an effective, yet simple, inexpensive – and potentially transformative – way to deliver vaccines,” says Laura Novotny, one of the study researchers.

Nontypeable Haemophilus influenzae (NTHi) is one of the three main bacterial causes of otitis media (OM), an infection or inflammation of the middle ear that often afflicts children.

Given that infections are currently managed with antibiotics, the emergence of antibiotic-resistant microorganisms is a major cause of concern.

Though surgery to insert tubes through the tympanic membrane relieves painful symptoms, the procedure is invasive and requires the child to be under general anaesthesia.

Considering all this, the researchers say that it is necessary to develop different ways to treat or preferably prevent this disease.

“We have designed several vaccine candidates which target proteins on the outer surface of this bacterium. Previous work in our lab showed that after immunization by injection, each of the three vaccine candidates prevented experimental ear infections caused by NTHi. In this study, we now wanted to test an alternative but potentially equally effective method to deliver a vaccine,” says Novotny.

The method, known as transcutaneous immunization, involved placing a droplet of each vaccine onto the ear and rubbing it into the skin.

During the study, the researchers immunized four groups of chinchillas with one of the three vaccine candidates. A fourth group received a placebo.

Each vaccine was placed on the ears of chinchillas once a week for three weeks. All animals were then inoculated with NTHi through the nose and directly into the middle ears.

Animals that received the vaccines were able to very rapidly reduce, or completely eliminate NTHi from the nose and ears, but animals that received a placebo did not. (ANI)

Scientists testing vaccine to prevent colon cancer

Washington, Mar 20 (ANI): Researchers at the University of Pittsburgh School of Medicine have begun testing a vaccine to prevent colon cancer.

If shown to be effective, it might spare patients the risk and inconvenience of repeated invasive surveillance tests, such as colonoscopy, that are now necessary to spot and remove precancerous polyps.

In a new approach for cancer prevention, the new vaccine is directed against an abnormal variant of a self-made cell protein called MUC1, which is altered and produced in excess in advanced adenomas and cancer.

“By stimulating an immune response against the MUC1 protein in these precancerous growths, we may be able to draw the immune system’s fire to attack and destroy the abnormal cells. That might not only prevent progression to cancer, but even polyp recurrence,” Schoen said.

According to co-author Olivera Finn, Ph.D., professor and chair of the Department of Immunology at Pitt’s School of Medicine, MUC1 vaccines have been tested for safety and immunogenicity in patients with late-stage colon cancer and pancreatic cancer.

“Patients were able to generate an immune response despite their cancer-weakened immune systems. Patients with advanced adenomas are otherwise healthy and so they would be expected to generate a stronger immune response. That may be able to stop precancerous lesions from transforming into malignant tumours,” she said.

About a dozen people have received the experimental vaccine so far, and the researchers intend to enroll another 50 or so into the study. (ANI)