Department of Plastic, Reconstructive and Hand Surgery, Amsterdam UMC-location VUmc, De Boelelaan 1117, PO Box 7057, 1007 MB, Amsterdam, The Netherlands.
Department of Dermatology, ReSculpt Clinic, Amsterdam, The Netherlands.
Aesthetic Plast Surg. 2021 Aug;45(4):1748-1759. doi: 10.1007/s00266-021-02306-3. Epub 2021 Apr 28.
Late inflammatory reactions (LIRs) are the most challenging complications after filler use. The immune system plays a prominent role in its etiology, albeit to an unknown extent. Bacterial contamination in situ has been hypothesized to be causative for LIRs. How this relates to the immunological processes involved is unknown. This article aims to provide an overview of immunological and bacterial factors involved in development of LIRs.
We undertook a systematic literature review focused on immunological factors and microbiota in relation to LIRs after filler use. This systematic review was performed in accordance with the PRISMA guidelines. PubMed, EMBASE and the Cochrane databases were searched from inception up to August 2019. Included studies were assessed for the following variables: subject characteristics, number of patients, primary indication for filler injection, implant type/amount and injection site, type of complication, follow-up or injection duration, study methods, type of antibiotics or medical therapies and outcomes related to microbiota and immunological factors.
Data on immunological factors and bacterial contamination were retrieved from 21 included studies. Notably, the presence of histocytes, giant cells and Staphylococcus epidermidis within biopsies were often associated with LIRs.
This review provides a clear overview of the immunological factors associated with LIRs and provides a hypothetical immunological model for development of the disease. Furthermore, an overview of bacterial contamination and associations with LIRs has been provided. Follow-up research may result in clinical recommendations to prevent LIRs.
This journal requires that authors assign a level of evidence to each article. For a full description of these Evidence-Based Medicine ratings, please refer to the Table of Contents or the online Instructions to Authors- www.springer.com/00266. .
迟发性炎症反应(LIRs)是填充剂使用后最具挑战性的并发症。免疫系统在其发病机制中起着突出的作用,尽管其作用程度尚不清楚。原位细菌污染被假设为 LIRs 的原因。这与涉及的免疫过程有何关系尚不清楚。本文旨在概述与填充剂使用后 LIRs 发展相关的免疫学和细菌因素。
我们进行了一项系统的文献综述,重点关注与填充剂使用后 LIRs 相关的免疫学因素和微生物组。这项系统综述是根据 PRISMA 指南进行的。从开始到 2019 年 8 月,我们在 PubMed、EMBASE 和 Cochrane 数据库中进行了搜索。纳入的研究评估了以下变量:受试者特征、患者数量、填充剂注射的主要适应证、植入物类型/数量和注射部位、并发症类型、随访或注射持续时间、研究方法、抗生素或医学治疗类型以及与微生物组和免疫学因素相关的结果。
从 21 项纳入的研究中获取了关于免疫学因素和细菌污染的数据。值得注意的是,活检中存在组织细胞、巨细胞和表皮葡萄球菌常与 LIRs 相关。
本综述提供了与 LIRs 相关的免疫学因素的清晰概述,并提供了疾病发展的假设性免疫学模型。此外,还提供了细菌污染及其与 LIRs 相关的概述。后续研究可能会产生预防 LIRs 的临床建议。
证据水平 III:本杂志要求作者为每篇文章分配一个证据水平。有关这些循证医学评级的完整描述,请参阅目录或在线作者指南-www.springer.com/00266。