Completed Digestion, Kidneys & Other Organs Infection & Immunity

Cutaneous Immunology

In plain English

AI plain-English summary

The skin’s immune system fails to repair its own barrier in eczema, allowing allergens and microbes to trigger chronic inflammation. This matters because atopic eczema is one of the most common skin diseases in the UK, often linked to asthma and hay fever. Current treatments rely on topical immune suppressants that manage symptoms but do not cure the disease and carry side effects. The fundamental gap is that scientists do not fully understand the sequence of events between a broken skin barrier and the resulting inflammation. The research aims to map those steps, focusing on two concrete goals: finding ways to repair the skin barrier itself, and identifying which newly discovered immune cells drive the inflammation. If successful, this could lead to treatments that prevent eczema from developing in the first place, rather than just suppressing symptoms after the fact. The findings may also improve how vaccines are delivered through the skin, making them more effective. This is primarily fundamental science—understanding the basic biology of skin immunity. Past work in cutaneous immunology has already transformed treatments for psoriasis and melanoma, so a deeper grasp of these mechanisms could similarly open unexpected therapeutic avenues.

View original technical description
We are working towards treatment and prevention of immune-mediated skin disease. The skin is often the first point of contact with pathogens and allergens, but relatively little is understood about how the cutaneous immune system clears these challenges. Such knowledge is vitally important to understanding the mechanisms of skin disease and related diseases, and for developing more effective ways of cutaneous drug and vaccine delivery. It is increasingly clear that skin barrier dysfunction is an important first step in the development of atopic eczema, one of the commonest skin diseases in the UK, and often associated with asthma and rhinitis. The barrier dysfunction promotes entry of allergens and microbes which eventually lead to skin inflammation. The latter is treated with topical immune suppressants, but these are not curative and also carry risks of side effects. We wish to understand the steps linking barrier dysfunction and skin inflammation, as these will provide opportunities for new treatments. In particular, we will explore ways to repair barrier function and to understand the roles of novel immune cells in contributing to the inflammation. These findings will have implications for atopic eczema, but also for other forms of inflammatory skin disease and indeed for the improvement of vaccine delivery in to the skin.

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Researchers

Graham Ogg (Principal Investigator)

Related Research

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Role of CD1a-reactive fungal lipid-specific T cells in atopic cutaneous inflammation
MRC/ucb adi 2018
Understanding immune-related toxicities through multifacet profiling

Original classification

Intramural

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