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Target Rheumatoid Arthritis

Contents

Introduction

Around 1000 BC, Indian Hindus believed that arthritis was a form of serious organic malfunction. By the fifth century BC, Hippocrates, the ‘Father of Medicine’, considered it to be caused by poisons in the body which could be relieved by draining. Only 150 years ago, bleeding to remove poison was still practised. By 1900, medical opinion had changed and doctors viewed arthritis as a result of infection. Operations to remove the teeth, tonsils and appendix to eliminate the ‘offending’ tissue were commonplace. Today we recognise many forms of arthritis with numerous causes. Rheumatoid arthritis (RA) is considered to be one of a group of illnesses called autoimmune diseases, in which the body’s defence system turns upon itself to cause inflammation and tissue destruction.

As long ago as 1899, aspirin was introduced to treat inflammation, but it was only about 50 years ago that the pharmaceutical industry entered the scene in earnest as it began to search for more powerful and effective alternatives. A breakthrough came with the pioneering work of Sir John Vane and his colleagues in the late 1960s, when they discovered how aspirin worked. From then on, it became possible to take a more rational approach, generating a large family of aspirin-like medicines which can ease pain and inflammation.

The search for medicines to prevent the joint destruction caused by RA was less successful, and most of those used today were found by chance after their introduction for other diseases. The first, gold therapy, was initiated in 1928, based on the belief that RA was related to tuberculosis, where gold salts had some effect. Since then, an assortment of unrelated medicines has been introduced, but these are not a cure and their effectiveness in reducing long-term joint damage remains unclear.

Today there are grounds for optimism as we begin at last to understand the true nature of RA. These insights are leading to a range of new biological medicines. Many are the products of genetic engineering and some are already being used in clinical trials. Hopefully, these will prove of value in treatment, but at least they should shed light on the mechanisms of RA and how new medicines can be developed.

The cost to society of RA is considerable. Detailed studies in the early 1990s showed that the annual cost of RA was about £380 million for healthcare services, around £60 million in laboratory tests, and £40 million in medicines costs. When indirect costs, such as loss of income, benefits and social services costs and inflation are added in, today’s annual bill is likely to be close to £1 billion per year.

This booklet provides some basic information about RA and describes the contribution being made by the pharmaceutical industry towards finding new and better treatments for it. It also seeks to give a glimpse into the future and to describe why this is an exciting time in RA research - one that offers new hope for everyone affected by this painful and debilitating condition.

 

Acknowledgements

The ABPI wishes to thank member companies for the information provided in the preparation of this booklet. The booklet was researched and written by Dr Mike Hall, who would like to acknowledge the help of Arthritis Care and other charities for their help. Dr J C Buckland-Wright is thanked for permitting the use of his microfocal X-ray data. Roche Products Ltd kindly provided the MRI image of animal cartilage. The illustration on page 18 was kindly supplied by Dorling Kindersley. The remaining photographs are from the Science Photo Library.

 

 
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