Department of Dermatology, Erasmus Medical Center, Rotterdam, The Netherlands.
Department of Molecular Cell Biology and Immunology, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
J Cosmet Dermatol. 2023 Feb;22(2):458-463. doi: 10.1111/jocd.15098. Epub 2022 Jul 31.
To date, it is unknown why some individuals develop late-onset inflammatory adverse events after treatment with fillers. These events may result from various factors, including an immunological response of the adaptive immune system.
In a pilot study, we looked for evidence that is there a relation between late-onset inflammatory adverse events and the presence of immune cells surrounding the injected filler.
We included 47 patients, of whom 20 experienced late-onset inflammatory adverse events to different fillers (inflammatory group) and 27 who did not (reference group). A biopsy was taken from the area of the adverse event. Hematoxylin-eosin staining and immunohistochemistry analysis with CD3 (T-cells) and CD68 (macrophages) on paraffin tissue sections was used to assess the biopsies.
Immune cells were found in biopsies obtained from 18 of 47 patients: Nine biopsies from the inflammation group and nine from the reference group. All these 18 cases showed CD68-positive immune cells. Virtually no CD3-positive immune cells were found.
Our results indicate that there is no T-cell activity in biopsies from areas with late-onset adverse events after filler injections. The macrophages found in the biopsies are probably not responsible for the inflammatory response.
迄今为止,尚不清楚为什么一些人在接受填充物治疗后会出现迟发性炎症性不良反应。这些事件可能由多种因素引起,包括适应性免疫系统的免疫反应。
在一项初步研究中,我们寻找了证据来证明迟发性炎症性不良反应与注射填充物周围免疫细胞的存在之间是否存在关系。
我们纳入了 47 名患者,其中 20 名患者在不同的填充物(炎症组)治疗后出现迟发性炎症性不良反应,27 名患者没有(参考组)。对不良反应部位进行活检。使用苏木精-伊红染色和 CD3(T 细胞)和 CD68(巨噬细胞)在石蜡组织切片上的免疫组化分析来评估活检。
在 47 名患者中的 18 名患者的活检中发现了免疫细胞:炎症组 9 例,参考组 9 例。所有这 18 例均显示 CD68 阳性免疫细胞。几乎没有发现 CD3 阳性免疫细胞。
我们的结果表明,在填充物注射后迟发性不良反应区域的活检中不存在 T 细胞活性。在活检中发现的巨噬细胞可能不是炎症反应的原因。