Division of Nephrology, Miami Transplant Institute, University of Miami Miller School of Medicine, Miami, Florida.
Clin J Am Soc Nephrol. 2017 Sep 7;12(9):1529-1533. doi: 10.2215/CJN.09180816. Epub 2016 Oct 18.
By definition, viral-associated GN indicates the direct pathogenic relationship between active viral replication and the development of acute GN. This definition is in sharp contrast to the semantic label and pathophysiologic foundation behind postinfectious GN that uniquely develops only during a period of resolved and absent active infection. The primary example of postinfectious GN are the glomerular lesions described after a pharyngeal or cutaneous streptococcal infection and do not represent the clinical or immunologic pattern seen with viral-associated GN. Hepatitis B (HBV) is the most common chronic viral infection in the world affecting >400 million people which is more than double the prevalence of chronic HIV and hepatitis C carriers combined. In addition, 10%-20% of HBV patients may be coinfected with hepatitis C and 5%-10% will have coinfection with HIV. Being able to distinguish the different types of GN seen with each viral infection is essential for the practicing clinician as each virus requires its own specific antiviral therapy. HBV-induced immune complex disease with renal injury lies on one end of the spectrum of disorders that occurs after a prolonged chronic carrier state. On the opposite end of the spectrum are renal diseases that develop from acute or subacute viral infections. One important glomerular lesion in this category is the association of collapsing FSGS with acute active cytomegalovirus, Epstein-Barr virus, and parvovirus B19 infection. The data supporting or disproving this relationship for each of these viruses will be discussed. A second renal manifestation of acute viral infections often occurs with many different sporadic or epidemic infections such as dengue and hantavirus and can lead to a transient proliferative GN that resolves upon viral clearance. The complex interplay of HBV and all viruses with the immune system provides conceptual lessons on the pathophysiology of immune complex GN that can be applied to all infection-related renal disease and plays an integral role in developing an approach to therapeutic intervention.
根据定义,病毒相关性 GN 表明急性 GN 的发生与病毒的活跃复制之间存在直接的致病关系。这一定义与感染后 GN 的语义标签和病理生理基础形成鲜明对比,感染后 GN 仅在已解决且不存在活跃感染的时期才会独特地发展。感染后 GN 的主要例子是在咽或皮肤链球菌感染后描述的肾小球病变,并不代表与病毒相关性 GN 相关的临床或免疫模式。乙型肝炎 (HBV) 是世界上最常见的慢性病毒感染,影响超过 4 亿人,是慢性 HIV 和丙型肝炎携带者总和的两倍多。此外,10%-20%的 HBV 患者可能同时感染丙型肝炎,5%-10%的患者可能同时感染 HIV。对于临床医生来说,能够区分每种病毒感染引起的不同类型的 GN 是至关重要的,因为每种病毒都需要其特定的抗病毒治疗。HBV 诱导的免疫复合物疾病伴肾损伤位于长期慢性携带者状态后发生的一系列疾病的一端。在光谱的另一端是由急性或亚急性病毒感染引起的肾脏疾病。在这一类中一个重要的肾小球病变是与急性活动性巨细胞病毒、EB 病毒和细小病毒 B19 感染相关的塌陷性 FSGS。将讨论支持或反驳这些病毒中每一种病毒的关系的数据。急性病毒感染的另一种肾脏表现通常发生在许多不同的散发性或流行性感染中,如登革热和汉坦病毒感染,并可导致一过性增殖性 GN,随着病毒清除而缓解。HBV 和所有病毒与免疫系统的复杂相互作用为免疫复合物 GN 的病理生理学提供了概念性的经验教训,这些经验教训可应用于所有与感染相关的肾脏疾病,并在制定治疗干预方法方面发挥重要作用。