Molecular Study of Skin Proteins Uncovers Predisposition to Eczema

Researchers from Newcastle University in the United Kingdom and Stiefel – a GlaxoSmithKline company – report their findings in the Journal of Allergy and Clinical Immunology.

Lead investigator Nick Reynolds, a professor of dermatology at Newcastle University who also works as a skin and eczema specialist in Newcastle’s Royal Victoria Infirmary, says that their discovery “reinforces the importance of filaggrin deficiency leading to problems with the barrier function in the skin and predisposing someone to eczema.”

He and his colleagues also believe that the study could lead to the development of drugs that target the underlying causes of eczema rather than just alleviate the symptoms.

Model of human skin with eczema

The exact causes of eczema are unknown. However, research reveals that it is likely to arise from a combination of genetic and environmental factors and probably involves dysfunction of both the skin barrier and the immune system. People with eczema may also develop asthma and hay fever.

  • Eczema may worsen or improve over time.
  • However, for many people, it is a life- long illness.
  • People with eczema may also be more prone to skin infections.

To further investigate the role of filaggrin, the researchers developed a 3- D model of human skin, in which, using molecular tools, they made the epidermis (the outside layer) deficient in filaggrin.

The model closely mimics what happens in the skin of people with eczema.

Using the model, the researchers were able to map the proteins and signaling pathways that lie “downstream” of filaggrin, and thus observe how the absence of the protein altered them.

They identified a number of signaling mechanisms that regulate inflammation, cell structure, stress response, and the function of the skin barrier.

The mapping of these pathways in the model appears to match that seen in people with eczema.

For example, the skin of people with active eczema has high levels of a protein coded by the gene KLK7. The team was able to show – from the model – that upregulation of KLK7 was one of the molecular consequences of filaggrin loss.

“This type of research allows scientists to develop treatments that target the actual root cause of the disease, rather than just managing its symptoms. Given the level of suffering eczema causes, this is a pivotal piece of research.”

Nina Goad, British Association of Dermatologists

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