Calabrò Maria Luisa, Sarid Ronit
Immunology and Molecular Oncology, Veneto Institute of Oncology IOV - IRCCS, Padua, Italy.
The Mina and Everard Goodman Faculty of Life Sciences & Advanced Materials and Nanotechnology Institute, Bar-Ilan University, Ramat-Gan, Israel.
Mediterr J Hematol Infect Dis. 2018 Nov 1;10(1):e2018061. doi: 10.4084/MJHID.2018.061. eCollection 2018.
The spectrum of lymphoproliferative disorders linked to human herpesvirus 8 (HHV-8) infection has constantly been increasing since the discovery of its first etiologic association with primary effusion lymphoma (PEL). PEL is a rapidly progressing non-Hodgkin's B-cell lymphoma that develops in body cavities in an effusional form. With the increase in the overall survival of PEL patients, as well as the introduction of HHV-8 surveillance in immunocompromised patients, the extracavitary, solid counterpart of PEL was later identified. Moreover, virtually all plasmablastic variants of multicentric Castleman's disease (MCD) developing in HIV-1-infected individuals harbor HHV-8, providing a strong etiologic link between MCD and this oncogenic herpesvirus. Two other pathologic conditions develop in HIV-1-infected persons concomitantly with MCD: MCD with plasmablastic clusters and HHV-8-positive diffuse large B-cell lymphoma not otherwise specified (HHV-8+ DLBCL NOS), the first likely representing an intermediate stage preceding the full neoplastic form. MCD in leukemic phase has also been described, albeit much less commonly. The germinotropic lymphoproliferative disorder (GLPD) may resemble extracavitary PEL, but develops in immune competent HHV8-infected individuals, and, unlike the other disorders, it responds well to conventional therapies. Almost all HHV-8-mediated lymphoproliferative disorders are the result of an interaction between HHV-8 infection and a dysregulated immunological system, leading to the formation of inflammatory niches in which B cells, at different developmental stages, are infected, proliferate and may eventually shift from a polyclonal state to a monoclonal/neoplastic disorder. Herein, we describe the association between HHV-8 and lymphoproliferative disorders and highlight the predominant distinctive features of each disease.
自首次发现人类疱疹病毒8型(HHV-8)感染与原发性渗出性淋巴瘤(PEL)存在病因学关联以来,与HHV-8感染相关的淋巴增殖性疾病谱一直在不断扩大。PEL是一种进展迅速的非霍奇金B细胞淋巴瘤,以渗出形式在体腔中发生。随着PEL患者总体生存率的提高,以及免疫功能低下患者中HHV-8监测的引入,PEL的腔外实性对应物随后被发现。此外,在HIV-1感染个体中发生的几乎所有多中心Castleman病(MCD)的浆母细胞变体都携带HHV-8,这在MCD与这种致癌疱疹病毒之间建立了强有力的病因学联系。另外两种病理状况在HIV-1感染个体中与MCD同时出现:伴有浆母细胞簇的MCD和未另行说明的HHV-8阳性弥漫性大B细胞淋巴瘤(HHV-8+ DLBCL NOS),前者可能代表完全肿瘤形式之前的中间阶段。白血病期的MCD也有报道,尽管较为少见。亲嗜性淋巴增殖性疾病(GLPD)可能类似于腔外PEL,但发生在免疫功能正常的HHV-8感染个体中,并且与其他疾病不同,它对传统疗法反应良好。几乎所有HHV-8介导的淋巴增殖性疾病都是HHV-8感染与免疫调节系统失调相互作用的结果,导致形成炎症微环境,不同发育阶段的B细胞在其中被感染、增殖,并最终可能从多克隆状态转变为单克隆/肿瘤性疾病。在此,我们描述HHV-8与淋巴增殖性疾病之间的关联,并强调每种疾病的主要显著特征。