Münz Christian
Viral Immunobiology, Institute of Experimental Immunology, University of Zürich, Winterthurerstrasse 190, 8057 Zürich, Switzerland.
Cancers (Basel). 2023 Dec 7;15(24):5739. doi: 10.3390/cancers15245739.
The oncogenic and persistent Epstein Barr virus (EBV) is carried by more than 95% of the human adult population. While asymptomatic in most of these, EBV can cause a wide variety of malignancies of lymphoid or epithelial cell origin. Some of these are also associated with co-infections that either increase EBV-induced tumorigenesis or weaken its immune control. The respective pathogens include Kaposi-sarcoma-associated herpesvirus (KSHV), and human immunodeficiency virus (HIV). In this review, I will discuss the respective tumor entities and possible mechanisms by which co-infections increase the EBV-associated cancer burden. A better understanding of the underlying mechanisms could allow us to identify crucial features of EBV-associated malignancies and defects in their immune control. These could then be explored to develop therapies against the respective cancers by targeting EBV and/or the respective co-infections with pathogen-specific therapies or vaccinations.
超过95%的成年人群携带致癌性且具持续性的爱泼斯坦-巴尔病毒(EBV)。虽然大多数携带者没有症状,但EBV可引发多种起源于淋巴或上皮细胞的恶性肿瘤。其中一些还与共感染有关,这些共感染要么增加EBV诱导的肿瘤发生,要么削弱其免疫控制。相关病原体包括卡波西肉瘤相关疱疹病毒(KSHV)和人类免疫缺陷病毒(HIV)。在这篇综述中,我将讨论各自的肿瘤实体以及共感染增加EBV相关癌症负担的可能机制。更好地理解潜在机制可以使我们识别EBV相关恶性肿瘤的关键特征及其免疫控制缺陷。然后可以通过针对EBV和/或采用病原体特异性疗法或疫苗接种来针对各自的共感染,探索开发针对这些癌症的治疗方法。