处于免疫衰老和肿瘤发生十字路口的巨细胞病毒

Fidaa Bouezzedine, Ranim El Baba, S. Morot-Bizot, M. Diab‐Assaf, G. Herbein
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摘要

人类巨细胞病毒(HCMV)的基因组约为235kb,是一种普遍存在的人类疱疹病毒,感染40%至95%的人群。尽管HCMV感染通常是无症状的,并会导致微妙的临床症状,但它可以促进强大的免疫反应并建立终身潜伏期。此外,在免疫功能低下的宿主中,包括艾滋病患者、移植受者和发育中的胎儿,它可能导致严重疾病。免疫衰老,定义为免疫系统的改变,主要与衰老有关,最近受到了相当大的关注。衰老的特征是炎症升高,因此被认为是“炎症”的有力因素,主要通过肿瘤坏死因子-α(TNF-α)、白细胞介素-6(IL-6)和C反应蛋白(CRP)水平以及潜在的病毒感染(例如巨细胞病毒(CMV))来测量。炎症导致衰老相关分泌表型(SASP)。HCMV与免疫系统的加速衰老以及几种与年龄相关的疾病显著相关,这些疾病会积累并随后恶化免疫反应,因此与老年人的死亡率、疫苗效力下降、严重疾病和肿瘤有关。HCMV引发或加剧免疫衰老;另一方面,免疫反应减弱和炎症有利于病毒的再激活,并突出了HCMV在衰老和病毒相关肿瘤中的作用。HCMV再激活导致连续的裂解和潜伏病毒周期可能有助于HCMV基因组变异。除了HCMV的肿瘤调节作用和转化能力外,免疫特权肿瘤微环境被认为是肿瘤进展和侵袭性的主要因素。因此,HCMV、免疫衰老和癌症之间的相互作用将有助于发现新的治疗方法,这些方法靶向HCMV,并作为免疫反应增强剂,主要用于对抗预后不良的癌症,尤其是老年人群。
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Cytomegalovirus at the crossroads of immunosenescence and oncogenesis
Human cytomegalovirus (HCMV), whose genome is around 235 kb, is a ubiquitous human herpesvirus that infects between 40% and 95% of the population. Though HCMV infection is commonly asymptomatic and leads to subtle clinical symptoms, it can promote robust immune responses and establish lifelong latency. In addition, in immunocompromised hosts, including individuals with acquired immunodeficiency syndrome (AIDS), transplant recipients, and developing fetuses it can lead to severe diseases. Immunosenescence, well-defined as the alterations in the immune system, is linked mainly to aging and has been recently gathering considerable attention. Senescence was characterized by an elevated inflammation and hence considered a powerful contributor to “inflammaging” that is measured mainly by tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6), and C-reactive protein (CRP) levels as well as latent viral infections, for instance, cytomegalovirus (CMV). Inflammaging resulted in a senescence-associated secretory phenotype (SASP). HCMV is markedly associated with accelerated aging of the immune system as well as several age-associated diseases that accumulate and subsequently deteriorate the immune responses, thus have been linked to mortality, declined vaccine efficacy, serious diseases, and tumors in the elderly. HCMV triggers or exacerbates immunosenescence; on the other hand, the weakened immune responses and inflammaging favor viral reactivation and highlight the role of HCMV in aging as well as viral-associated tumors. HCMV reactivation resulting in sequential lytic and latent viral cycles could contribute to HCMV genomic variability. Besides the oncomodulatory role and transforming capacities of HCMV, the immune-privileged tumor microenvironment has been considered the main element in tumor progression and aggressiveness. Therefore, the interplay between HCMV, immunosenescence, and cancer will aid in discovering new therapeutic approaches that target HCMV and act as immune response boosters mainly to fight cancers of poor prognosis, particularly in the elderly population.
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