2023
DOI: 10.1016/j.mad.2023.111779
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Acceleration of melanocyte senescence by the proinflammatory cytokines IFNγ and TNFα impairs the repigmentation response of vitiligo patients to narrowband ultraviolet B (NBUVB) phototherapy

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Cited by 4 publications
(3 citation statements)
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“…NB-UVB phototherapy acts as an efficient treatment modality to induce skin re-pigmentation in stable vitiligo. Although NB-UVB phototherapy was confirmed to be an efficient treatment option, the repigmentation responses to that PT differs significantly in various vitiligo cases and re-pigmentation might only appear after several months of treatment [13] . Thus, the combination of NBUVB and another treatment modality could be used in an effort to achieve faster and greater re-pigmentation.…”
Section: Discussionmentioning
confidence: 99%
“…NB-UVB phototherapy acts as an efficient treatment modality to induce skin re-pigmentation in stable vitiligo. Although NB-UVB phototherapy was confirmed to be an efficient treatment option, the repigmentation responses to that PT differs significantly in various vitiligo cases and re-pigmentation might only appear after several months of treatment [13] . Thus, the combination of NBUVB and another treatment modality could be used in an effort to achieve faster and greater re-pigmentation.…”
Section: Discussionmentioning
confidence: 99%
“…In addition, melanocytes and fibroblasts present a senescence pattern in vitiligo skin ( 140 142 ). IFNγ and TNF-α were shown to induce senescence in melanocytes ( 143 , 144 ), and it would be interesting to evaluate the impact of type-2 cytokines in senescence in vitiligo given that IL-13 can promote senescence in submandibular glands ( 145 ). Nonetheless, type-2-related cytokines may also be protective in some subclinical subsets of vitiligo, since dupilumab induced or worsened vitiligo in AD patients ( 100 , 146 148 ).…”
Section: Vitiligomentioning
confidence: 99%
“…The MMP9 inhibitor GM6001 has been shown to decrease the production of the soluble form of the receptor KIT by suppressing ectodomain shedding 194 . Since MMP9's proteolytic activity is also involved generating soluble KITLG, 166 this raises the question of whether administering the MMP9 inhibitor GM6001 could be used to block the formation of soluble KITLG, thereby increasing the amount of membrane‐bound KITLG and providing potential hair and skin pigmentation‐stimulatory effects.…”
Section: Potential Therapeutic Targets/agentsmentioning
confidence: 99%