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脂磷壁酸和透明质酸的分子量可以解释透明质酸填充剂引发的迟发性炎症反应。

Lipoteichoic acid and molecular weight of hyaluronic acid could explain the late inflammatory response trigger by hyaluronic acid fillers.

机构信息

Medical Department Dorsia Clinics, Madrid, Spain.

Centro de Biología Molecular Severo Ochoa, Madrid, Spain.

出版信息

J Cosmet Dermatol. 2022 Nov;21(11):5610-5613. doi: 10.1111/jocd.15243. Epub 2022 Jul 27.

DOI:10.1111/jocd.15243
PMID:35839384
Abstract

INTRODUCTION

Hyaluronic acid is a safe dermal filler, but sometimes late granuloma is generated. This adverse effect is an inflammatory process, and its causes are not clear. Late granuloma generation could be due to the reaction to residual components of the bacterial wall present into hyaluronic acid, such as lipoteichoic acid (LTA). Other possibility is hyaluronic acid degraded could be trigger this inflammatory reaction.

OBJECTIVE

Study possible molecular mechanism that could be implicated into the late granuloma formation. We wonder whereas inflammatory response activation is triggered by lower molecular weight hyaluronic acid or Gram-positive bacterial components as LTA.

METHODS

We analyzed one adverse case generated by hyaluronic acid injections. Our study with one nodule through chemical and immunofluorescence histologic technics.

RESULTS

In this case, observe a late granuloma without infectious process. Histological analysis shown few large Langerhans cells around fillers and multiple immunological cells infiltrated. Immunofluorescent study shown immunological cells (CD45 positives cells) with high TLR2 expression (hyaluronic acid and LTA receptor).

LIMITATIONS

The difficulty of obtaining biopsy samples of nodules implies that the number of cases analyzed is very low.

CONCLUSION

New model is proposed in which weight of hyaluronic acid and LTA could be able to trigger inflammation. This process could be mediated by TLR2 expressed in infiltrated immune cells.

摘要

简介

透明质酸是一种安全的真皮填充剂,但有时会产生迟发性肉芽肿。这种不良反应是一种炎症过程,其原因尚不清楚。迟发性肉芽肿的产生可能是由于对透明质酸中存在的细菌细胞壁残留成分(如脂磷壁酸(LTA))的反应。另一种可能性是透明质酸的降解可能引发这种炎症反应。

目的

研究可能涉及迟发性肉芽肿形成的分子机制。我们想知道,炎症反应的激活是由低分子量透明质酸还是革兰氏阳性细菌成分(如 LTA)引发的。

方法

我们分析了一例由透明质酸注射引起的不良反应病例。我们通过化学和免疫荧光组织学技术对一个结节进行了研究。

结果

在这个病例中,观察到一个没有感染过程的迟发性肉芽肿。组织学分析显示填充剂周围有少量大的朗格汉斯细胞和多个免疫细胞浸润。免疫荧光研究显示免疫细胞(CD45 阳性细胞)高表达 TLR2(透明质酸和 LTA 受体)。

局限性

获得结节活检样本的困难意味着分析的病例数量非常少。

结论

提出了一种新的模型,其中透明质酸和 LTA 的重量可能能够引发炎症。这个过程可能是由浸润免疫细胞中表达的 TLR2 介导的。

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