2022
DOI: 10.1111/phpp.12848
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A postulated model for photoimmunopathogenesis of chronic actinic dermatitis around adaptive immunity, including Th17 cells, Tregs, TRMs, cytotoxic T cells, and/or common‐γ chain receptor+ cells

Abstract: Background/Purpose: The pathogenesis of chronic actinic dermatitis (CAD) is more complicated than other photodermatoses. However, the relationship between the clinical severity of CAD and the offending photocontact or contact allergens or both, and the correlations of CAD immunopathogenesis with the immunoregulatory molecules involved in adaptive immunity are yet to be investigated. Methods:We performed phototesting with broad-spectrum ultraviolet (UV) B, UVA, and visible light to establish the presence of pho… Show more

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Cited by 5 publications
(3 citation statements)
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References 23 publications
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“…Inhibition of this pathway using JAK inhibitors could be a promising treatment for a variety of skin disorders. 19 , 20 These inhibitors target various cell types, including CD8-positive T cells, and suppress the interferon-gamma and interleukin pathways by blocking the action of four key tyrosine kinases: JAK1, JAK2, JAK3, and tyrosine kinase 2 (TYK2). Tofacitinib, a selective oral Janus Kinase inhibitor (JAK1 inhibitor), has proven effective in treating several T cell-mediated dermatoses such as psoriasis, atopic dermatitis, dermatomyositis, alopecia areata, and vitiligo, which do not respond to classical immunosuppressive therapy.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Inhibition of this pathway using JAK inhibitors could be a promising treatment for a variety of skin disorders. 19 , 20 These inhibitors target various cell types, including CD8-positive T cells, and suppress the interferon-gamma and interleukin pathways by blocking the action of four key tyrosine kinases: JAK1, JAK2, JAK3, and tyrosine kinase 2 (TYK2). Tofacitinib, a selective oral Janus Kinase inhibitor (JAK1 inhibitor), has proven effective in treating several T cell-mediated dermatoses such as psoriasis, atopic dermatitis, dermatomyositis, alopecia areata, and vitiligo, which do not respond to classical immunosuppressive therapy.…”
Section: Discussionmentioning
confidence: 99%
“…Several studies have reported that CAD development is linked to dysregulated inflammation and oxidative stress. 5 , 20 Additionally, it’s also observed that CAD patients are more susceptible to infections following skin biopsy. 3 Photo allergy triggers the alteration of endogenous skin antigens, followed by inflammation mediated by CD8+ T cells, a process similar to the delayed-type hypersensitivity in allergic contact dermatitis.…”
Section: Discussionmentioning
confidence: 99%
“… 18 It was reported that UV-induced CD3+, CD4+, and CD8+ cells increased in the more severe CSS-CAD subgroup and mediated their suppressive function by releasing immune regulatory cytokines such as IL-4 and IL-10. 19 Therefore, it has been speculated that immune imbalance plays an important role in the pathogenesis of CAD. A retrospective study of CAD patients over a 5-year period found that 16 (21.6%) of CAD patients with an early age of onset had an atopic history.…”
Section: Discussionmentioning
confidence: 99%