Soffritti Irene, D'Accolti Maria, Maccari Clara, Bini Francesca, Mazziga Eleonora, de Conto Flora, Calderaro Adriana, Arcangeletti Maria-Cristina, Caselli Elisabetta
Section of Microbiology, Department of Chemical, Pharmaceutical and Agricultural Sciences, and LTTA, University of Ferrara, 44121 Ferrara, Italy.
Department of Medicine and Surgery, University of Parma, 43126 Parma, Italy.
Microorganisms. 2022 Aug 8;10(8):1600. doi: 10.3390/microorganisms10081600.
Systemic sclerosis (SSc) is a severe autoimmune disease likely triggered by genetic and environmental factors, including viral infections. Human cytomegalovirus (HCMV) and human herpesvirus 6A species (HHV-6A) have been associated with SSc, based on in vivo and in vitro evidence, but the data are still inconclusive. Furthermore, despite both viruses being highly prevalent in humans and able to exacerbate each other's effects, no data are available on their joint effects. Hence, we aimed to study their simultaneous impact on the expression of cell factors correlated with fibrosis and apoptosis in in vitro coinfected fibroblasts, representing the main target cell type in SSc. The results, obtained by a microarray detecting 84 fibrosis/apoptosis-associated factors, indicated that coinfected cells underwent higher and more sustained expression of fibrosis-associated parameters compared with single-infected cells. Thus, the data, for the first time, suggest that HCMV and HHV-6A may cooperate in inducing alterations potentially leading to cell fibrosis, thus further supporting their joint role in SSc. However, further work is required to definitively answer whether β-herpesviruses are causally linked to the disease and to enable the possible use of targeted antiviral treatments to improve clinical outcomes.
系统性硬化症(SSc)是一种严重的自身免疫性疾病,可能由遗传和环境因素引发,包括病毒感染。基于体内和体外证据,人巨细胞病毒(HCMV)和人疱疹病毒6A种(HHV-6A)与系统性硬化症有关,但数据仍无定论。此外,尽管这两种病毒在人类中高度流行且能够相互加剧彼此的影响,但关于它们的联合作用尚无数据。因此,我们旨在研究它们对体外共感染成纤维细胞中与纤维化和细胞凋亡相关的细胞因子表达的同时影响,成纤维细胞是系统性硬化症中的主要靶细胞类型。通过检测84种纤维化/细胞凋亡相关因子的微阵列获得的结果表明,与单感染细胞相比,共感染细胞的纤维化相关参数表达更高且更持久。因此,这些数据首次表明,HCMV和HHV-6A可能协同作用诱导潜在导致细胞纤维化的改变,从而进一步支持它们在系统性硬化症中的联合作用。然而,需要进一步的研究来明确回答β疱疹病毒是否与该疾病存在因果关系,并使靶向抗病毒治疗有可能用于改善临床结果。