AI Article Synopsis

  • Topical keloid therapy often uses triamcinolone acetonide (TA) injections, but it has a high recurrence rate and side effects.
  • Mesenchymal stem cells (MSCs) can lower fibroblast activity in keloids, and this study evaluates the effectiveness of umbilical cord MSCs (UC-MSC) and their conditioned medium (UC-CM) compared to TA.
  • Results showed the UC-MSC group had the most significant reduction in keloid volume and improvement in symptoms, indicating that UC-MSC and UC-CM are more effective alternatives to TA for treating keloids.

Article Abstract

Topical keloid therapy is performed with triamcinolone acetonide (TA) intralesional injection. However, the recurrence rate is high with various side effects. Mesenchymal stem cells (MSCs) have high proliferative abilities and reduce the activity and proliferation of fibroblast cells in keloids. To overcome the costs and limitations, conditioned medium (CM) is used. This study aims to evaluate feasibility of intralesional injection of umbilical cord MSC (UC-MSC) and conditioned medium (UC-CM) compared to TA for keloid therapy. Twenty-four patients with keloids who met the inclusion criteria were included, randomized into three treatment groups and then got assessed for the sociodemographic data, keloid volume, histopathology (type 1:3 collagen ratio), interleukin-10 (IL-10) levels and Patient and Observer Scar Assessment Scale (POSAS) score during visits. Largest volume regression occurred in the UC-MSC group, followed by UC-CM and then the TA group (UC-MSC: 45.32% ± 2.61%; UC-CM: 43.61% ± 3.67%; TA: 28.34% ± 3.81%; p = 0.003). Similar pattern was also observed in increase in IL-10 levels, the decrease in POSAS scores and the reduction of type 1:3 collagen ratio. Hence, UC-MSC and UC-CM are promisingly more effective than TA for keloid therapy, showcasing their superiority in reducing keloid volume, symptoms and type 1:3 collagen ratio, as well as increasing the levels of IL-10.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10828519PMC
http://dx.doi.org/10.1111/iwj.14460DOI Listing

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