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乳房植入物及假体周围组织中与乳房植入物相关的间变大细胞淋巴瘤的微生物组学研究。

Insights into the Microbiome of Breast Implants and Periprosthetic Tissue in Breast Implant-Associated Anaplastic Large Cell Lymphoma.

机构信息

Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, Missouri, USA.

Center for Women's Infectious Disease Research, Washington University School of Medicine, St. Louis, Missouri, USA.

出版信息

Sci Rep. 2019 Jul 17;9(1):10393. doi: 10.1038/s41598-019-46535-8.

Abstract

Though rare, breast implant-associated anaplastic large cell lymphoma (BIA-ALCL), a CD30+ T-cell lymphoma associated with textured breast implants, has adversely impacted our perception of the safety of breast implants. Its etiology unknown, one hypothesis suggests an initiating inflammatory stimulus, possibly infectious, triggers BIA-ALCL. We analyzed microbiota of breast, skin, implant and capsule in BIA-ALCL patients (n = 7), and controls via culturing methods, 16S rRNA microbiome sequencing, and immunohistochemistry. Alpha and beta diversity metrics and relative abundance of Gram-negative bacteria were calculated, and phylogenetic trees constructed. Staphylococcus spp., the most commonly cultured microbes, were identified in both the BIA-ALCL and contralateral control breast. The diversity of bacterial microbiota did not differ significantly between BIA-ALCL and controls for any material analyzed. Further, there were no significant differences in the relative abundance of Gram-negative bacteria between BIA-ALCL and control specimens. Heat maps suggested substantial diversity in the composition of the bacterial microbiota of the skin, breast, implant and capsule between patients with no clear trend to distinguish BIA-ALCL from controls. While we identified no consistent differences between patients with BIA-ALCL-affected and contralateral control breasts, this study provides insights into the composition of the breast microbiota in this population.

摘要

虽然罕见,但与纹理乳房植入物相关的乳腺癌相关间变性大细胞淋巴瘤(BIA-ALCL),一种 CD30+T 细胞淋巴瘤,已经对我们对乳房植入物安全性的看法产生了不利影响。其病因不明,一种假说认为,起始炎症刺激物,可能是感染,引发了 BIA-ALCL。我们通过培养方法、16S rRNA 微生物组测序和免疫组织化学分析,分析了 BIA-ALCL 患者(n=7)和对照组的乳房、皮肤、植入物和包膜中的微生物群。计算了 alpha 和 beta 多样性指标以及革兰氏阴性菌的相对丰度,并构建了系统发育树。在 BIA-ALCL 和对侧对照乳房中均鉴定出最常见的培养微生物葡萄球菌属。在任何分析的材料中,BIA-ALCL 和对照组之间的细菌微生物群多样性没有显著差异。此外,BIA-ALCL 标本和对照标本之间革兰氏阴性菌的相对丰度也没有显著差异。热图表明,皮肤、乳房、植入物和包膜中细菌微生物群的组成存在很大差异,但没有明确的趋势将 BIA-ALCL 与对照组区分开来。虽然我们没有在 BIA-ALCL 受累乳房和对侧对照乳房之间发现一致的差异,但这项研究提供了对该人群乳房微生物群组成的深入了解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f215/6637124/c636b0823d82/41598_2019_46535_Fig1_HTML.jpg

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