New immunotherapy strategy hope for psoriasis and vitiligo patients

by IANS |



Sydney, Dec 2 (IANS) Researchers have discovered distinct mechanisms controlling different types of immune cells, and found that, by precisely targeting these mechanisms, they could selectively eliminate "problematic cells" and reshape the skin's immune landscape, a finding that can help patients with autoimmune skin disorders such as psoriasis and vitiligo.


Human skin is packed with specialised immune cells that protect against infections and cancer and promote healing. These cells, called tissue-resident T cells or TRM cells, stay in place to fight infections and cancerous cells in the skin. However, when not controlled properly, some of these skin TRM cells can contribute to psoriasis and vitiligo.


This research is the first to describe the unique elements that control various types of skin TRM cells in animal models, offering precise targets for potential treatment strategies, said lead first author Dr Simone Park, from University of Melbourne's Doherty Institute in Australia.


"Specialised immune cells in our skin are diverse: many are critical to prevent infection and cancer, but others play a big role in mediating autoimmunity," said Dr Park.


"We discovered key differences in how distinct types of skin T cells are regulated, allowing us to precisely edit the skin's immune landscape in a targeted way."


In the study, published in the journal Science, the research team harnessed this new knowledge to eliminate 'problematic' cells that can drive autoimmune disorders, while preserving the 'good' ones that are essential to maintain protective immunity.


The findings could pave the way for more precise and long-lasting therapies for skin disease.


"Skin conditions like psoriasis and vitiligo are difficult to treat long-term. The T cells driving disease are hard to remove, so patients often need life-long treatment. Our approach has the potential to revolutionise the way we treat these skin disorders, significantly improving outcomes for people dealing with challenging skin conditions," said Professor Laura Mackay, Laboratory Head and Immunology Theme Leader at the Doherty Institute.


With the study demonstrating successful removal of specific skin T cells in animal models, further research is necessary to validate the efficacy of these strategies in human subjects. Dr Park hopes the study will inspire the development of new treatments for skin disease.


"These discoveries bring us one step closer to developing new drugs that durably prevent autoimmune skin disorders without compromising immune protection," said Park.



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