Skin resident T cells Implications for immune homeostasis and disease

Open Access
Authors
  • T. dos Reis Matos
Supervisors
  • M.A. de Rie
  • R.A. Clark
Cosupervisors
  • M.B.M. Teunissen
Award date 08-11-2019
ISBN
  • 9789463325233
Number of pages 428
Organisations
  • Faculty of Medicine (AMC-UvA)
Abstract
A population of memory T cells stay resident (TRM) at all times in peripheral tissues, such as the skin. These TRM cells function as alarming sensors, cytotoxic killers and provide a long-term local memory that can spread widely when re-infected with the same antigen. However, when dysfunctional, skin located TRM cells can have a profound role in various skin disorders, including psoriasis and vitiligo. TRM cell-mediated skin disorders often show lesions with fixed cut-offs from healthy skin. Typically, these lesions resolve when treated, but tend to recur at the exact same location when treatment is discontinued. In the context of transplantation, TRM cells can react to allogeneic cells promoting tissue inflammation. Targeting TRM cells could lead to efficient treatment for these skin disorders. Yet, we still lack therapies capable of affecting only TRM cells. Phototherapy is perhaps the most ancient form of treatment in dermatology, but remains a valuable treatment option for TRM-associated diseases. More research has to be done on safety of blocking and inducing TRM cells in human. Thankfully, novel research technologies and methodologies are emerging. Much can be learned about this new subset of T cells. Using this knowledge in therapeutic and preventive therapy development could lead to a better quality of life of many patients suffering from skin disorders.
Document type PhD thesis
Language English
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