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Through biomedical research, we aim to understand what causes MS. This helps us develop more effective treatments for MS, and ultimately stop it from occurring.

Current projects

 

Identifying inflammatory immune cells in the spinal fluid of people with relapsing-remitting MS 

Dr John Curnow
University of Birmingham
£148,007

What’s the project about?

There are many different types of immune cell. This project is looking at aggressive immune cells that cause damage in MS and others that suppress immune damage.

This study aims to answer the following two questions:

  1. What particular types of immune cells are present?
  2. How does the presence of these immune cells relate to the symptoms of MS?

Researchers will take small amounts of blood and spinal fluid from people with MS and other neurological conditions, and also from people without MS or other neurological conditions. They will look at immune cells present in the blood and spinal fluid to see whether they cause or suppress the damage seen in MS.

How will it help people with MS?

This project will significantly add to our understanding of how the immune system is changed in people with MS. This could help us to identify which cells are responsible for the damage in MS and which could potentially be targeted for the development of new therapies for MS. 

Knowing how these cells relate to the symptoms of MS may also help us manage and treat MS more effectively.

The difference you can make

Understanding the immune system and its role in MS is a key part of planning future treatment strategies for people living with the condition.

By supporting projects like this you could help us get one step closer to understanding how the immune system works in people with MS.

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Understanding genetic variation in multiple sclerosis 

Dr Stephen Sawcer
University of Cambridge
£72,000

What’s the project about?

Researchers already know that MS is more common in the relatives of people with MS, and that this is because they share DNA.

A particular gene called CD86 is linked to the switching on of white blood cells, which make up part of the immune system. This study will look the levels and functions of the CD86 gene in 200 people.

How will it help people with MS?

A drug called Abatacept is known to act on the CD86 gene and blocks it from switching on white blood cells. This drug has been shown to help people with Rheumatoid Arthritis and is now being looked at for treating MS. This study hopes to provide researchers with further information about which people with MS might respond best to this treatment by looking at their levels of the CD86 gene.

The difference you can make

Nobody understands what causes MS, and we desperately need more therapies.

Donate and help us better understand MS and identify potential new treatments. 

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Imaging demyelination and remyelination in people with MS 

Dr Nikos Evangelou
Nottingham University Hospital NHS Trust
£164,752

What’s the project about?

The brain is made up of two types of tissue: grey matter and white matter.

The aim of this project is to better visualise and understand lesions in the brain using specialised imaging. This will help us understand what causes disability in MS.

Using the most advanced MRI scanner (7 Tesla) Dr Evangelou will scan people with MS using a technique that can help us visualise myelin. His team will be able to study the grey matter in a detail that has not been achieved before.

How will it help people with MS?

By studying people with MS at different stages of disability, the study will provide a better view of how grey matter demyelination affects all types of MS. Results from this study could also greatly improve the screening process used by large clinical trials of potential treatments for myelin repair.

The difference you can make

Our aim is to beat MS. You can help us by supporting research like this – research that could help us understand the causes of MS and develop more effective treatments.

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Studying how mitochondria function in MS

Prof. Kenneth Smith
University College London
£219,956

What’s the project about?

Recent findings from this group show that some of the symptoms of MS may be due to a shortage of energy in brain cells.

The aim of this project is to:

  • Understand how the brain cells become short of energy
  • Develop therapies to protect against energy shortage. Such therapies should preserve function and protect against permanent damage to brain cells.

Mitochondria are the structures inside cells that act as the powerhouse, producing energy for the cell to use. Professor Smith’s team will look in detail at the mitochondria in brain cells to see how they react to the damage caused by MS.

How will it help people with MS?

Researchers have already got their first clues about how the mitochondria might be damaged. Once researchers understand more, they can test therapies that protect mitochondria.

The difference you can make

Our aim is to beat MS. You can help us achieve that aim by supporting research like this – research that may help us to understand the causes of MS so that we can develop more effective treatments.

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Are infections related to disability progression in people with MS? (Phase II) 

Dr Ian Galea
University of Southampton
£31,801

What’s the project about?

The long term aim of this project is to explore whether infections, such as colds or chest infections, might affect the progression of disability in MS.

This project is the second stage of a longer term study. During the fist stage the researchers explored the possibility of using information from the Sylvia Lawry Centre (which contains the largest collection of MS data in the world) to see if infections play a role in the progression of disability.

The results of this first stage were positive and in this second stage researchers will analyse the information that has been collected.

How will it help people with MS?

It's important to identify factors which affect progression in MS, because current treatments are effective in suppressing relapses but are not as effective in preventing progression of the condition.

If this research shows that infections lead to disability progression, actively preventing infections in people affected by MS may become a clinical priority.

The difference you can make

One of our research priorities is to find out more about progressive forms of MS.

Please help us achieve this goal by donating to the MS Society.

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What controls the blood brain barrier in MS?

Dr Ignacio Romero
The Open University
£205,122

What’s the project about?

Under normal circumstances cells and molecules are prevented from entering the brain by the blood brain barrier.

During an MS attack, the blood brain barrier opens and allows immune cells to enter the brain – where they can attack myelin. Little is understood about what causes the blood brain barrier to open and close – but there is some indication that a class of small molecules called microRNAs may play a role in controlling the blood brain barrier.

In this three year study, the researchers will:

  • determine if microRNAs play a role in controlling the blood brain barrier using tissue samples from the MS Society Tissue Bank
  • use laboratory models of MS to see if changing the levels of specific microRNAs will change the way the blood brain barrier works

How will it help people with MS?

This is an early laboratory study that will help researchers find out how the blood brain barrier works – and what changes occur in people with MS that cause it to open. Knowledge gained from this study may lead researchers to develop treatments that prevent the blood brain barrier from opening in people with MS.

The difference you can make

Research like this is essential if we are to find out more about what causes the blood brain barrier to open. Please donate to the MS Society so that we can continue to fund research of the highest quality.

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MS Society Tissue Bank



Professor Richard Reynolds
Imperial College London
£1,027,846

What’s the project about?

In July 2009, we awarded a research grant for nearly £1 million to the MS Society Tissue Bank  at Imperial College London to support the work for a further five years.

The Tissue Bank has been supported by the MS Society since 1998 and it allows people with, and without, MS to donate their brain and spinal cord to MS research.

Researchers at the Tissue Bank then process and store the samples so they can be used for vital MS research into the causes of MS, and potential treatments for the condition.

How will it help people with MS?

Research using tissue samples from humans is vital if we are to understand the causes of MS and develop new effective treatments for the condition. The MS Society provides a valuable resource for researchers around the world who are seeking answers to these very important questions.

The difference you can make

The MS Society Tissue Bank relies on brain and spinal cord donations from people with and without MS to continue their valuable work.

Find out how you can pledge to donate by calling 020 7594 9734. By working together we can beat MS.

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Understanding how the body’s immune system damages nerve fibres in MS

Dr Sandra Amor
Queen Mary, University of London
£180,589

What’s the project about?

Previous research suggests that in MS the body’s immune system not only attacks myelin, but also a protein found in the nerve fibres themselves called neurofilament light (NF-L).

This three year project will use laboratory models of MS to find out whether the immune system attacks NF-L, and improve our understanding of how it causes damage to the nerve fibres in MS.

How will it help people with MS?

Damage to nerve fibres can lead to irreversible disability in people with MS. This project will answer much-needed questions about what causes irreversible damage to the brain in people with MS, and how we can prevent it.

The difference you can make

One of our key priorities is to find new treatments for people living with progressive forms of MS. If you would like to add to our knowledge about what causes disability progression in people with MS, and find ways to prevent it then please support this project.

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Understanding the immune system in MS

Dr Anne Astier
University of Edinburgh
£341,161

What’s the project about?

In MS, a specific type of immune cell called a T-cell attacks myelin.

Attacks on myelin lead to relapses in people with MS. Early research suggests that a molecule called CD46, found in T-cells, does not work as it should in people with MS.

In this three year project researchers will compare T-cells from people with MS to T-cells from people without MS.

They will look very closely at how CD46 protein on T-cells from people with MS behaves differently than in people without MS, including how it is made.

How will it help people with MS?

This project will hopefully get us closer to understanding how the immune system behaves differently in people with MS. Knowledge gained from this project may be used to develop new treatment strategies for people living with the condition.

The difference you can make

Understanding the immune system and its role in MS is a key part of planning future treatment strategies for people living with the condition.

By supporting projects like this you could help get us one step closer to understanding exactly how MS causes damage.

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Do grey matter lesions relate to cognitive difficulties in people with MS?

MRI machine at Institute of NeurologyProf David Miller
Institute of Neurology
£391,533 

What’s the project about?

The brain is divided into two types of tissue (grey matter and white matter).

In the past, researchers were unable to see lesions in the grey matter of people with MS. But new, more powerful MRI machines mean that it’s now possible for researchers to see lesions in these areas of the brain.

Professor Miller and his team will look at detailed MRI scans in people with MS and people without MS to see whether lesions in the brain’s grey matter match up with disability in people with MS. They will specifically look at cognitive disability.

How will it help people with MS?

There is currently no way of predicting what symptoms people with MS will develop, or how severely they will be affected.

If researchers can demonstrate that grey matter lesions are linked with cognitive symptoms in people with MS, they might be able to use this information to eventually predict which people with MS will go on to develop cognitive difficulties.

The difference you can make

Thanks to the generosity of our donors we were able to purchase a brand new state-of-the-art MRI scanner for the Institute of Neurology, which has made this work possible.

Please consider donating to MS research so that we can continue funding vital work like this.

Find out about our other project researching the causes, and more effective treatments for, MS with a more powerful MRI scanner

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Understanding risk factors associated with MS

Ruth Dobson
Queen Mary University, London
£186,418
Three years

What’s the project about?

MS lesionThe causes of MS are not known, but researchers believe that there may be multiple risk factors involved in the development of MS. Both environmental and genetic factors have been associated with MS.

This three year project will set out to understand the factors that influence an individuals risk of developing MS.

Researchers will recruit:

  • 100 people with MS
  • 120 of their siblings who do not have MS
  • 100 people who do not have a relative with MS

They will explore whether there are any risk factors specifically associated with MS such as vitamin D levels, exposure to specific infections, and genetic differences.

How will it help people with MS?

Researchers are planning to use the knowledge gained during this study to identify risk factors associated with MS.

If researchers can better understand the risk factors involved in MS they may, one day, be able to put in place strategies that lower an individuals risk of developing the condition.

The difference you can make

We are dedicated to supporting research that will help us understand the causes of MS so that we can develop better treatments for the condition. Please support research like this so that we can, one day, beat MS.

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Understanding the genetics of MS in South Asian populations

Dr Omar Malik
Imperial College London
£107,400

What’s the project about?

MS is thought to be an autoimmune condition, where the body’s own immune system mistakenly attacks healthy tissue.

In the case of MS the immune system attacks myelin that coats nerve fibres in the brain and spinal cord.

A group of genes called human leukocyte antigens (HLA) have an important role in regulating the immune system and preventing autoimmunity. The risk of a person having MS is sometimes related to whether they have a particular HLA gene.

In this one year study the researchers plan to analyse DNA obtained from blood samples from around 200 people with MS and 200 people without MS from the South Asian population.

The aim is to improve our understanding of the role that HLA genes play in increasing the risk of MS in the South Asian population, which previously has received little attention.

How will it help people with MS?

The results from this study will improve our understanding of the role of HLA genes in the development of MS.

Increasing our knowledge in this area helps us to understand more about the causes of MS and develop strategies to treat and reduce an individual’s risk of developing MS.

The difference you can make?

Nobody understands what causes MS and researchers are working hard to put the pieces together.

Donate to this project and help us find the causes of MS.

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Learning more about T-cells’ role in MS

Professor David Wraith
University of Bristol
£323,694

What’s the project about?

In MS, a type of immune cell called a T-cell can mistakenly attack myelin that forms a protective layer around nerve fibres. T-cells that attack myelin are called myelin-reactive T-cells.

However, a new type of T-cell called a regulatory T-cell, or T-reg cell, is thought to be able to ‘talk’ to myelin-reactive T-cells and dampen them down. This may prevent myelin-reactive T-cells from attacking myelin and causing an MS attack.

How will it help people with MS?

In this four year project, researchers will use sophisticated imaging techniques and laboratory models of MS to further our understanding of how regulatory T-cells interact and ‘talk’ with myelin-reactive T-cells.

They hope to find a way to ‘reprogramme’ myelin-reactive T cells to stop them attacking myelin.

The difference you can make

Nobody understands what causes MS and researchers are working hard to put the pieces together. Donate to MS research and help us understand the causes of MS.

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Mapping the genes of MS

Professor George Ebers
University of Oxford
£103,947

What’s the project about?

The major histocompatability complex (MHC) is a part of the human genome that contains many genes important in influencing how the immune system works.

Previous work has identified a number of genes in the MHC that are linked with MS and can alter a person’s risk of developing the condition.

In this three year project, researchers will use a number of different state-of-the-art laboratory techniques to study in detail MHC genes in DNA samples from 20 people with MS.

They will look at how these genes function and see how their function might be altered in people with MS.

How will it help people with MS?

Increasing our knowledge in this area helps us to understand more about the causes of MS and to develop strategies to reduce a person’s risk of developing the condition.

The difference you can make

Nobody understands what causes MS and researchers are working hard to put the pieces together. Donate to MS research and help us find the causes of MS. 

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Understanding childhood MS

Dr Evangeline Wassmer 
Institute of Child Health, Birmingham Children’s Hospital
£379,444

What’s the project about?

Lucy, 5, who has MSIt is estimated that around one in 20 people with MS develop symptoms before the age of 16. Until recently, childhood MS was not well known and researchers still understand very little about how MS affects children.

The aim of this five year project is to find out how many children in the UK are affected by a first MS-like attack and which of those are most likely to go on to develop MS.

The researchers estimate that approximately 250 children in the UK will experience an MS-like attack in one year, of which 80 will go on to be diagnosed with MS. 

The research plan is divided into two parts:

  • In the first part of this study, the researchers plan to collect clinical data over a period of three and half years from as many of these children as possible
  • In the second part of the study, the researchers plan to follow a group of children with MS over a longer period of time, initially for five years 

The researchers also hope to follow a group of children with MS both during the course of this project and beyond into adulthood, providing the basis for an extremely valuable long-term study on the causes and progression of childhood MS.

How will it help people with MS?

Understanding how MS affects children will help researchers and doctors determine what treatments and services are appropriate for children and their families.

Dr Wassmer and her team are also looking at the possible causes of MS in children and they hope this will help them understand more about what causes MS in adults.

The difference you can make

By supporting this project not only will you be helping us to improve our understanding of childhood MS but you will also help to raise awareness of childhood MS amongst paediatricians, resulting in prompt diagnosis and treatment. This project is jointly funded with Action Medical Research.

Useful Links

Childhood demyelination study group 
British paediatric surveillance unit

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Finding a way to make oligodendrocytes

Dr Sybil Stacpoole
University of Cambridge
£103,596

What’s the project about?

In MS the immune system attacks a protein called myelin which forms a protective layer around nerve fibres of the brain and spinal cord.

Myelin is made by cells called oligodendrocytes. Over time the ability of oligodendrocytes in people with MS to repair myelin can fail.

The aim of this three year research project is to find a way to make embryonic stem cells into oligodendrocytes in the laboratory. The researchers will then test the ability of these new oligodendrocytes to repair myelin damage in laboratory models of MS.

How will it help people with MS?

When myelin repair fails, the exposed nerve fibres themselves can then be damaged beyond repair, leading to an accumulation of disability in the later stages of MS.

Understanding how oligodendrocytes can be made in the laboratory will help researchers to develop and test treatments that may promote myelin repair in people with MS.

The difference you can make

Stem cells are a useful tool for understanding how MS damage occurs (and in finding out how we can repair that damage). You can help fund this research by donating today.

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Using genetics to predict who will respond to beta-interferon

Professor Alastair Compston
University of Cambridge
£258,530

What’s the project about?

Beta-interferon is a disease modifying drug (DMD) used to reduce the number of relapses that people with relapsing remitting MS experience.

Some people respond well to beta-interferon, but not everyone does, and others experience bad reactions to the drug.

This three year project will identify genes that help determine whether someone responds well to beta-interferon treatment.

Professor Compston’s team will analyse blood samples from:

  • 100 people who respond well
  • 100 people who don’t respond well
  • 50 people who have experienced a bad reaction to beta-interferon

They will analyse participants’ genes to see if there is any way to predict who is likely to respond well to treatment.

How will it help people with MS?

We currently have no way of knowing whether somebody is likely to respond well to beta-interferon. We hope this research will eventually help people with MS and their doctors make more informed decisions about their treatment options.

The difference you can make

By supporting MS research you could help save people from months or even years of ineffective treatment and side effects.

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Can the body’s own stem cells be stimulated to make myelin?

Professor Charles ffrench-Constant
University of Edinburgh
£193,483

What’s the project about?

In MS the immune system attacks a protein called myelin which forms a protective layer around nerve fibres of the brain and spinal cord. Over time the ability to repair myelin can fail.

In this three year project Professor ffrench-Constant and his team at the MS Society Edinburgh Centre for Translational Research will use laboratory models of MS to investigate how myelin repair can occur.

They will attempt to find a way to stimulate adult stem cells in the brain to repair myelin.

How will it help people with MS?

There are currently no therapies available that repair damage to myelin, something that could potentially benefit everyone with MS.

Professor ffrench-Constant and his team in Edinburgh will be working with the MS Society Cambridge Centre for Myelin Repair to develop and test potential therapies that promote myelin repair in people with MS.

The difference you can make

Therapies that promote myelin repair are the missing link in MS treatment and researchers are working hard to make myelin repair a reality for people with MS.

Please help us achieve this goal by donating to vital MS research.

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Predicting who is likely to benefit from a potential new treatment for MS

Professor Chris Linington
University of Glasgow
£203,661 

What’s the project about?

Professor Linington’s group has recently discovered a set of molecules (called Neurofascin-specific autoantibodies) found in some people with MS that can cause damage to nerve fibres in laboratory models of MS.

People who have high levels of Neurofascin-specific autoantibodies may benefit from treatments that reduce their levels in the blood but it is currently impossible to predict which people would benefit from such treatments.

The Glasgow-based research team will develop a simple test to help determine who is likely to benefit from treatments that lower the levels of Neurofascin-specific autoantibodies in the blood.

How will it help people with MS?

We hope this work will provide us with tools to identify people with MS who might benefit from treatments that lower the levels of Neurofascin-specific autoantibodies so that we can eventually test those treatments in clinical trials.

The difference you can make

Your support for work like this will help speed this progress and will help researchers develop new treatments for people with MS as quickly as possible.

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Researching the causes, and more effective treatments for, MS with a more powerful MRI scanner

Professor David Miller
Institute of Neurology, University College London
£2,544,384

What’s the research about?

This funding has enabled Professor Miller and his team at the Institute of Neurology to buy a new, more powerful MRI (magnetic resonance imaging) scanner which can analyse brain and spinal cord tissue in more detail than was previously possible.

The new 3-Tesla scanner has replaced the previous scanner, which was 1.5-Tesla.

This is the only scanner dedicated solely to MS research in the UK.

How will it help people with MS?

The new scanner will be used to support a number of research projects within the UK and will hopefully help us to answer new questions about MS that researchers were previously unable to answer. Researchers will also use the new scanner to test potential treatments for MS.

The difference you can make

Nobody understands what causes MS and researchers are working hard to put the pieces together. Donate to MS research and help us find the causes of MS. 

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Page last updated: 09 May 2012