Mbarara University of Science and Technology, Mbarara, Uganda.
Department of Microbiology and Immunology, SUNY Upstate Medical University, Syracuse, New York, USA.
J Infect Dis. 2021 Jan 4;223(1):101-108. doi: 10.1093/infdis/jiaa340.
It has been demonstrated that activated mast cells (MCs) are enriched in Kaposi sarcoma (KS) tumors and contribute to the inflammatory microenvironment. Mechanisms driving MC activation, however, are incompletely understood. We sought to understand whether immunoglobulin E (IgE), a potent activator of MCs, was associated with KS incidence and severity. In a cross-sectional study of untreated human immunodeficiency virus (HIV)-infected adults with or without KS in Uganda, we found that patients with KS had higher plasma IgE levels than those without KS. After adjustment for age, sex, CD4+ T-cell count, and HIV RNA levels, there was a dose-response relationship between plasma IgE levels and the presence and severity of KS. Higher eosinophil counts were also associated with IgE levels, and plasma interleukin 33 concentrations were higher in individuals with KS. These findings suggest that IgE-driven atopic inflammation may contribute the pathogenesis of KS. Therapies targeting IgE-mediated MC activation thus might represent a novel approach for treatment or prevention of KS.
已经证明,活化的肥大细胞(MCs)在卡波济肉瘤(KS)肿瘤中丰富,并有助于炎症微环境。然而,驱动 MC 活化的机制尚不完全清楚。我们试图了解免疫球蛋白 E(IgE),一种 MCs 的有效激活物,是否与 KS 的发病和严重程度有关。在乌干达对未经治疗的人类免疫缺陷病毒(HIV)感染的成年人进行的一项横断面研究中,我们发现患有 KS 的患者的血浆 IgE 水平高于没有 KS 的患者。在调整年龄、性别、CD4+ T 细胞计数和 HIV RNA 水平后,血浆 IgE 水平与 KS 的存在和严重程度之间存在剂量反应关系。更高的嗜酸性粒细胞计数也与 IgE 水平相关,并且患有 KS 的个体的血浆白细胞介素 33 浓度更高。这些发现表明 IgE 驱动的特应性炎症可能有助于 KS 的发病机制。因此,针对 IgE 介导的 MC 活化的治疗方法可能代表治疗或预防 KS 的新方法。