Journal
FRONTIERS IN IMMUNOLOGY
Volume 12, Issue -, Pages -Publisher
FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2021.652191
Keywords
resident memory T cell (TRM); cutaneous lupus erythematosus (CLE); vitiligo; psoriasis; alopecia; dermatology; autoimmunity
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Funding
- UMass Research & Curriculum Exploration program
- Dermatology Foundation
- Target Identification in Lupus Award from the Lupus Research Alliance
- US Department of Defense Lupus Research Program [LR190030]
- NIH [R01 AR069114, R61 AR070302]
- Hartford Foundation
- Calder Research Scholar Award from the American Skin Association
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Tissue resident memory T cells (TRM) play a crucial role in the immune system by providing immediate and specific responses against pathogens re-infecting peripheral tissues. However, they have also been found to contribute to autoimmune diseases, where self-antigens continuously activate self-reactive TRM T cells, leading to destructive outcomes. This article focuses on how TRMs mediate disease in autoimmune skin conditions, such as vitiligo, psoriasis, cutaneous lupus erythematosus, alopecia areata, and frontal fibrosing alopecia.
Tissue resident memory T cells (TRM) are a critical component of the immune system, providing the body with an immediate and highly specific response against pathogens re-infecting peripheral tissues. More recently, however, it has been demonstrated that TRM cells also form during autoimmunity. TRM mediated autoimmune diseases are particularly destructive, because unlike foreign antigens, the self-antigens are never cleared, continuously activating self-reactive TRM T cells. In this article, we will focus on how TRMs mediate disease in autoimmune skin conditions, specifically vitiligo, psoriasis, cutaneous lupus erythematosus, alopecia areata and frontal fibrosing alopecia.
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