Circassia Achieves Positive Phase II Clinical Results With Ragweed Allergy T-Cell Vaccine


Written on February 13, 2010 – 5:30 pm | by admin

Circassia Ltd, a specialty biopharmaceutical company focused on allergy, announced that its ToleroMune(R) ragweed allergy T-cell vaccine achieved positive results in a recently completed phase II clinical trial. Ragweed allergy is particularly common in America, where it affects approximately 25% of the population. Circassia’s latest clinical results follow two earlier successful phase II studies with the company’s T-cell vaccine against cat allergy. The company has three additional phase II trials ongoing, targeting house dust mite and cat allergies, and plans to initiate three further studies in the coming months, extending the portfolio into the field of grass allergy.

The results from Circassia’s latest clinical study demonstrate that four doses of the ToleroMune T-cell vaccine greatly improved the allergic responses measured in the trial. The efficacy endpoints, which included the early phase skin response to a challenge dose of ragweed allergen, were measured both before and after the ragweed season. This response, which is commonly used by allergists to assess allergic status, showed a characteristic increase in the placebo group by the end of the ragweed season, resulting in values 37% higher than baseline. In contrast, the optimal ToleroMune T-cell vaccine regime reversed this seasonal increase and reduced it by a further 47% compared with the pre-ragweed season baseline. Throughout the study, the ToleroMune vaccines were safe and well tolerated, with a treatment-related safety profile similar to placebo.

“These highly encouraging clinical results further validate our unique T-cell vaccine approach to allergy therapy. Our ToleroMune technology has now shown its potential to address both ragweed and cat allergies, and we hope to extend this product range when we receive the results of our ongoing study in house dust mite allergy later this year,” said Steve Harris, Circassia’s CEO. “With three phase II studies now complete, our growing clinical database demonstrates the true potential of our ToleroMune T-cell vaccines. Unlike current immunotherapies, which require increasing doses over a number of months and several years of maintenance, ToleroMune therapy is short and simple, and minimises the risk of the severe and sometimes life-threatening side effects associated with many existing treatments.”

About Circassia’s allergy T-cell vaccines

Circassia’s range of allergy T-cell vaccines is based on its proprietary ToleroMune(R) technology. This technology utilises allergen epitopes to generate regulatory T cells that suppress allergic immune responses. Clinical results with Circassia’s cat allergy T-cell vaccine show that short treatment regimes can greatly reduce patients’ symptoms, without the need for adjuvants or other immune stimulators, while proving extremely well tolerated. As a result, the company’s allergy T-cell vaccines offer major potential clinical benefits compared with existing therapies, and consequently have significant market opportunities. Over 150 million people suffer from allergic rhinitis in the US and Europe, and the current treatment market is approximately $12 billion per year.

ToleroMune technology has additional potential regulatory and supply chain benefits. The short peptides utilised in Circassia’s vaccines are manufactured chemically, in contrast to existing allergen immunotherapies, which are purified from natural sources. Circassia’s approach applies the chemistry, manufacturing and control standards associated with conventional pharmaceuticals to its allergy T-cell vaccines. This fits with changes in the European regulatory environment, where authorities are increasingly treating allergen immunotherapies as pharmaceutical products, and requiring elimination of the batch-to-batch potency variability that is an intrinsic feature of many current treatments.

About Circassia

Circassia has a highly experienced management team with a proven track record in product development and commercialisation. Having successfully completed three fundraising rounds the company is backed by a syndicate of world-class venture capital and institutional investors, including Imperial Innovations, Invesco Perpetual, Goldman Sachs and Lansdowne Partners.

Source: Circassia Ltd

Brain Waves Show Patterns For Deciding Which Faces We Prefer


Written on February 11, 2010 – 6:16 pm | by admin

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Faces play a very important role in our social life. We make complex social decisions based on facial appearance. Extensive research has been made to identify a set of facial features which make a face attractive. Possibly no research is needed to predict which face a heterosexual male would prefer when asked to choose between Megan Fox (voted as one of the sexiest celebrities) and Jocelyn Wildenstein (voted as one of the ugliest celebrities).

But we know little how we make a preference decision when the two faces are closely matched (e.g., age, race, gender, gaze, facial attributes, facial emotion). Is there any specific brain activity pattern associated with our preference (or non-preference)? Can these patterns be identified before our conscious decision?

These problems were addressed by a neuroimaging study led by Joydeep Bhattacharya at Goldsmiths, University of London, where human volunteers were asked to make a preference decision between two faces which are closely matched. Faces were presented one after the other and volunteers were instructed to choose the face that they would most like to approach and to talk to. Their brain waves (electroencephalogram) were continuously recorded.

“We found specific brain activity patterns which correlate to the decision making process,” said Bhattacharya, “one pattern is specific to the face currently being looked at, and the other is specific to the face previously shown which is only available through mental recall, and surprisingly, both patterns occur well before the moment of conscious decision on which face is preferred. We also found some activity patterns which are possibly related to positive first impression effect.”

Does this mean that brain decides first and tells us later?

Bhattacharya remarked, “This is a tricky question which troubles both neuroscientists and philosophers alike. We cannot prove from the current study that this is indeed the case, but there is ample evidence that we are not fully aware of the constituent brain processes leading to a conscious decision. The real challenge is to predict the final conscious decision based on these pre-conscious neural activity patterns on trial by trial basis and in real-time.”

Other researchers involved with the study are Job Lindsen and Rhiannon Jones from Goldsmiths, University of London and Shinsuke Shimojo from California Institute of Technology, USA.

Source: Goldsmiths University of London

Exercise of the Week: Lunge – a hip flexor stretch


Written on February 10, 2010 – 10:57 pm | by admin

Most of us need to stretch our hip flexors. We get tight hip flexors from sitting too much, and some of us do exercises like running and biking that tighten the hip flexors.

Standing lunge is an easy hip flexor stretch. You can do it almost anywhere, anytime. It is a very good exercise to do as you are waiting for an exercise class to start (ever wonder what to do with yourself while waiting?). Read these directions for tips on doing the lunge in the way that brings the most benefit to your body. Learn the Lunge Stretch

Have the Exercise of the Week, along with other great Pilates info, sent directly to you each week in the Free Pilates Newsletter.

Gene Variant For Biological Ageing In Humans Discovered


Written on February 8, 2010 – 10:17 pm | by admin

Scientists from the UK and The Netherlands have identified for the first time a variant of a gene that is linked to biological ageing in humans and suggest the discovery will help us better understand cancer and diseases of ageing.

The findings of the study by researchers based at the University of Leicester and King’s College London, UK, and also at the University of Groningen in the Netherlands, were reported online in Nature Genetics on 7 February. The Wellcome Trust and the British Heart Foundation sponsored the work.

Professor Nilesh Samani, a British Heart Foundation Professor of Cardiology at the University of Leicester’s Department of Cardiovascular Sciences co-led the project and also co-wrote the paper. The other project co-leader was Professor Tim Spector from King’s College London, who is also director of the TwinsUK study.

In a press statement Samani explained that there are two forms of aging: chronological ageing and biological ageing. Chronological ageing is simply how much time has elapsed since you were born, whereas biological age is determined by certain cellular properties that make your cells younger or older than your chronological age.

One such cellular property is the length of the telomeres on the ends of your chromosomes. Every time a cell divides, its chromosomes are copied, and to preserve the information in the chromosome there are end bits that have no important DNA information: they are like buffers that protect the internal information of the chromosome, and with each replication, bits drop off the telomeres, but as long as there is still some left, the information in the chromosome is protected and passed on to the next cell generation.

Samani explained that:

“Individuals are born with telomeres of certain length and in many cells telomeres shorten as the cells divide and age. Telomere length is therefore considered a marker of biological ageing.”

“There is accumulating evidence that the risk of age-associated diseases including heart disease and some types of cancers are more closely related to biological rather than chronological age,” he added.

For the study, Samani, Spector and colleagues conducted a genome-wide association analysis of more than 500,000 genetic variations across the whole human genome to find variants sited near a gene called TERC. Altogether the analysis involved looking at the genes of over 12,000 individuals.

Spector explained that they looked at variants near TERC because the gene was already known to play a role in maitaining telomere length.

The researchers found that those individuals carrying a particular genetic variant had shorter telomeres, ie they looked biologically older.

“Given the association of shorter telomeres with age-associated diseases, the finding raises the question whether individuals carrying the variant are at greater risk of developing such diseases,” said Samani.

Spector said the findings suggest that some people are genetically programmed to age more quickly:

“The effect was quite considerable in those with the variant, equivalent to between 3-4 years of ‘biological aging” as measured by telomere length loss.”

He also said that this could mean that people with the variant may age even faster when exposed to other risks that are also “bad” for telomeres like smoking, obesity and lack of exercise. They could “end up several years biologically older or succumbing to more age-related diseases,” he added.

“Common variants near TERC are associated with mean telomere length.”
Veryan Codd, Massimo Mangino, Pim van der Harst, Peter S Braund, Michael Kaiser, Alan J Beveridge, Suzanne Rafelt, Jasbir Moore, Chris Nelson, Nicole Soranzo, Guangju Zhai, Ana M Valdes, Hannah Blackburn, Irene Mateo Leach, Rudolf A de Boer, Wellcome Trust Case Control Consortium, Alison H Goodall, Willem Ouwehand, Dirk J van Veldhuisen, Wiek H van Gilst, Gerjan Navis, Paul R Burton, Martin D Tobin, Alistair S Hall, John R Thompson, Tim Spector & Nilesh J Samani.
Nature Genetics, Published online: 07 February 2010.
DOI:10.1038/ng.532

Source: University of Leicester.

Written by: Catharine Paddock, PhD
Copyright: Medical News Today
Not to be reproduced without permission of Medical News Today