The study was recently published in the Journal of Investigative Dermatology.

Eczema, also known as atopic dermatitis (AD), causes the skin's protective barrier to break down, making it more vulnerable to foreign entities that can cause itching, inflammation, dryness and further degradation of the skin's protective barrier.

"The symptoms people often experience with eczema make them more likely to avoid going outside their homes or to work," says the study's senior author, Dr. David Granville, a professor in UBC's faculty of medicine and researcher at VCHRI. "It is estimated that the annual cost of eczema in North America is over $5.5 billion because of how it impacts people's health and well-being."

The Granzyme B enzyme is positively correlated with itchiness and disease severity in eczema. Researchers found that Granzyme B weakens the skin barrier by cleaving through the proteins holding cells together making it easier for allergens to penetrate across.

"Between cells in our skin are proteins that anchor them tightly together," says Granville. "In some inflammatory diseases, such as eczema, Granzyme B is secreted by cells and eats away at those proteins, causing these bonds to weaken and the skin to become further inflamed and itchy."

Researchers found that by knocking out Granzyme B with genetic modification, or inhibiting it with a topical gel, they could prevent it from damaging the skin barrier and significantly reduce the severity of AD.

"Previous work had suggested that Granzyme B levels correlate with the degree of itchiness and disease severity in patients with atopic dermatitis; however, there was no evidence that this enzyme played any causative role," says Granville. "Our study provides evidence that topical drugs targeting Granzyme B could be used to treat patients with eczema and other forms of dermatitis."

Researchers aim to quell the root cause of eczema symptoms

Approximately 15-20 per cent of Canadians live with some form of AD, and among Canadian children under the age of five, AD affects between 10-15 per cent. Of those, around 40 per cent will experience symptoms of the disease for the rest of their lives.

AD is also associated with an increased risk of developing a host of other inflammatory conditions, including food allergies, asthma and allergic rhinitis.

"Atopic dermatitis is the leading non-fatal health burden attributable to skin diseases," says Dr. Chris Turner, the study's lead author and former UBC postdoctoral fellow in Granville's laboratory.

AD typically follows an itch-scratch cycle in which itchiness is followed by scratching and more itchiness. This cycle usually occurs during flare-ups, which can appear anytime, and sometimes weeks, months or years apart.

Corticosteroid creams are a common treatment for individuals with AD who experience more severe itching and rashes. However, these can thin the skin when used over a prolonged period of time, which can make skin more prone to damage and infection.

A gel or cream that stops or limits Granzyme B, thereby reducing the severity of AD, could be a safer and more effective long-term treatment.

"A gel or cream that blocks Granzyme B could have fewer if any side-effects and circumvent the itch-scratch cycle, making flare-ups less pronounced," says Turner

While a commercially available treatment is still a ways away, the researchers see great promise in this line of research and are pursuing further clinical trials into Granzyme B and Granzyme B inhibitors.

Story Source:

Materials provided by University of British Columbia. Note: Content may be edited for style and length.

Journal Reference:

1. Christopher T. Turner, Matthew R. Zeglinski, Katlyn C. Richardson, Stephanie Santacruz, Sho Hiroyasu, Christine Wang, Hongyan Zhao, Yue Shen, Roma Sehmi, Hermenio Lima, Gail M. Gauvreau, David J. Granville. GRANZYME B CONTRIBUTES TO BARRIER DYSFUNCTION IN OXAZOLONE-INDUCED SKIN INFLAMMATION THROUGH E-CADHERIN AND FILAGGRIN CLEAVAGE. Journal of Investigative Dermatology, 2020; DOI: 10.1016/j.jid.2020.05.095