Multidisciplinary Institute for Investigation in Pediatric Pathologies (IMIPP), CONICET-GCBA. Molecular Biology Laboratory, Pathology Division, Ricardo Gutiérrez Children's Hospital, Buenos Aires, Argentina.
Multidisciplinary Institute for Investigation in Pediatric Pathologies (IMIPP), CONICET-GCBA. Pathology Division, Ricardo Gutiérrez Children's Hospital, Buenos Aires, Argentina.
J Virol. 2022 Jan 12;96(1):e0143421. doi: 10.1128/JVI.01434-21. Epub 2021 Oct 13.
Macrophages can be polarized toward a proinflammatory phenotype (M1) (CD68) or to an anti-inflammatory one (M2) (CD163). Polarization can be triggered by cytokines such as IFN-γ for M1, or IL-10 and TGF-β, for M2. In the context of pediatric Epstein Barr virus (EBV) infection, little is known about macrophage polarization in EBV primary or persistent infection. When studying tonsils of patients undergoing primary infection (PI), healthy carrier (HC), reactivation (R), and not infected (NI), M1 profile prevailed in all infection status. However, an increase in M2 cells was observed in those patients with broader expression of latency antigens, in particular EBNA2. Tonsils from primary infected patients showed an increased IL-10 expression, whereas, unexpectedly, TGF-β expression correlated with M1 marker. Furthermore, an inverse correlation was demonstrated between CD68 and IFN-γ. Therefore, in the context of asymptomatic infection in children, M1 macrophage polarization prevails, even in the presence of IL-10 and TGF-Ꞵ immunomodulatory cytokines, and it might be independent from lymphomagenesis process. Our finding indicates that macrophages may have a significant plasticity in response to different types of extrinsic stimuli, and further studies are required to investigate M1 polarization under anti-inflammatory stimuli. Most studies on Epstein Barr virus (EBV) primary infection have been performed in adolescents and young adult populations with Infectious Mononucleosis (IM) in developed countries. Furthermore, studies related to macrophage polarization were assessed in EBV-associated lymphomas, but little is known about macrophage polarization in the context of primary infection at the site of viral entry and replication, the tonsils. Therefore, the aim of this study was to characterize macrophage response in children undergoing EBV primary or persistent infection, in order to enlighten the role of macrophages in viral pathogenesis, in a population with a high incidence of EBV-associated lymphomas in children younger than 10 years old. This study may contribute to explain, at least in part, the asymptomatic viral infection in children from an underdeveloped region, given that M1 polarization pattern prevails, but in a regulatory environment.
巨噬细胞可以向促炎表型(M1)(CD68)或抗炎表型(M2)(CD163)极化。极化可以由 IFN-γ 等细胞因子触发,用于 M1,或由 IL-10 和 TGF-β 触发,用于 M2。在小儿 EBV(EBV)感染的背景下,对于 EBV 原发性或持续性感染中的巨噬细胞极化知之甚少。在研究原发性感染(PI)、健康携带者(HC)、再激活(R)和未感染(NI)的患者扁桃体时,在所有感染状态下,M1 表型都占主导地位。然而,在那些潜伏抗原表达更广泛的患者中,观察到 M2 细胞增加,特别是 EBNA2。原发性感染患者的扁桃体表现出增加的 IL-10 表达,然而,出乎意料的是,TGF-β 表达与 M1 标志物相关。此外,还证明了 CD68 与 IFN-γ 之间存在负相关。因此,在儿童无症状感染的背景下,M1 巨噬细胞极化占主导地位,即使存在 IL-10 和 TGF-β 免疫调节细胞因子,并且它可能独立于淋巴瘤发生过程。我们的发现表明,巨噬细胞在对外源性刺激的反应中可能具有显著的可塑性,需要进一步研究以在抗炎刺激下研究 M1 极化。 大多数关于 EBV 原发性感染的研究都是在发达国家的青少年和年轻成人中进行的,他们患有传染性单核细胞增多症(IM)。此外,关于巨噬细胞极化的研究评估了 EBV 相关淋巴瘤,但对于原发性感染部位(扁桃体)中巨噬细胞极化知之甚少。因此,本研究的目的是描述经历 EBV 原发性或持续性感染的儿童的巨噬细胞反应,以阐明巨噬细胞在病毒发病机制中的作用,该研究人群中儿童期 EBV 相关淋巴瘤的发病率很高,年龄小于 10 岁。本研究至少可以部分解释欠发达地区儿童无症状病毒感染,因为 M1 极化模式占主导地位,但处于调节环境中。