Department of Laboratory Medicine and Pathology, University of Minnesota Medical School , Minneapolis, MN, USA ; Department of Pediatrics, University of Minnesota Medical School , Minneapolis, MN, USA.
Department of Laboratory Medicine and Pathology, University of Minnesota Medical School , Minneapolis, MN, USA.
Clin Transl Immunology. 2015 Feb 27;4(2):e33. doi: 10.1038/cti.2015.1. eCollection 2015 Feb.
Infectious mononucleosis is a clinical entity characterized by pharyngitis, cervical lymph node enlargement, fatigue and fever, which results most often from a primary Epstein-Barr virus (EBV) infection. EBV, a lymphocrytovirus and a member of the γ-herpesvirus family, infects at least 90% of the population worldwide, the majority of whom have no recognizable illness. The virus is spread by intimate oral contact among adolescents, but how preadolescents acquire the virus is not known. During the incubation period of approximately 6 weeks, viral replication first occurs in the oropharynx followed by viremia as early as 2 weeks before onset of illness. The acute illness is marked by high viral loads in both the oral cavity and blood accompanied by the production of immunoglobulin M antibodies against EBV viral capsid antigen and an extraordinary expansion of CD8(+) T lymphocytes directed against EBV-infected B cells. During convalescence, CD8(+) T cells return to normal levels and antibodies develop against EBV nuclear antigen-1. A typical clinical picture in an adolescent or young adult with a positive heterophile test is usually sufficient to make the diagnosis of infectious mononucleosis, but heterophile antibodies are not specific and do not develop in some patients especially young children. EBV-specific antibody profiles are the best choice for staging EBV infection. In addition to causing acute illness, long-term consequences are linked to infectious mononucleosis, especially Hodgkin lymphoma and multiple sclerosis. There is no licensed vaccine for prevention and no specific approved treatment. Future research goals are development of an EBV vaccine, understanding the risk factors for severity of the acute illness and likelihood of developing cancer or autoimmune diseases, and discovering anti-EBV drugs to treat infectious mononucleosis and other EBV-spurred diseases.
传染性单核细胞增多症是一种以咽炎、颈淋巴结肿大、疲劳和发热为特征的临床实体,主要由原发性 EBV(Epstein-Barr 病毒)感染引起。EBV 是一种淋巴亲嗜病毒,属于γ疱疹病毒家族成员,全球至少有 90%的人感染过 EBV,其中大多数人没有明显的疾病。病毒通过青少年之间的密切口腔接触传播,但尚未明确幼儿如何感染病毒。在大约 6 周的潜伏期内,病毒首先在口咽部复制,然后在疾病发作前 2 周左右发生病毒血症。急性疾病的特征是口腔和血液中的病毒载量均很高,同时产生针对 EBV 衣壳抗原的免疫球蛋白 M 抗体,并伴有针对 EBV 感染 B 细胞的 CD8+T 淋巴细胞的异常扩增。在恢复期,CD8+T 细胞恢复正常水平,针对 EBV 核抗原-1 的抗体形成。青少年或年轻成人中出现阳性异嗜性试验和典型临床表现通常足以诊断传染性单核细胞增多症,但异嗜性抗体不具有特异性,并且一些患者(尤其是幼儿)不会产生抗体。EBV 特异性抗体谱是分期 EBV 感染的最佳选择。除了引起急性疾病外,传染性单核细胞增多症还与长期后果相关,尤其是霍奇金淋巴瘤和多发性硬化症。目前尚无预防用的许可疫苗,也没有专门批准的治疗方法。未来的研究目标是开发 EBV 疫苗、了解急性疾病严重程度和发生癌症或自身免疫性疾病的风险因素,以及发现治疗传染性单核细胞增多症和其他 EBV 引发疾病的抗 EBV 药物。