Li Xuemeng, Kantola Kalle, Hedman Lea, Arku Benedict, Hedman Klaus, Söderlund-Venermo Maria
College of Veterinary Medicine, Northeast Agricultural University, Harbin, PR China.
Department of Virology, University of Helsinki, Helsinki, Finland.
J Gen Virol. 2015 Oct;96(10):3099-3108. doi: 10.1099/jgv.0.000253. Epub 2015 Jul 28.
Human bocavirus (HBoV) 1 is a widespread parvovirus causing acute respiratory disease in young children. In contrast, HBoV2 occurs in the gastrointestinal tract and is potentially associated with gastroenteritis, whilst HBoV3 and -4 infections are less frequent and have not yet been linked with human disease. Due to HBoV1 DNA persistence in the nasopharynx, serology has been advocated as a better alternative for diagnosing acute infections. In constitutionally healthy children, we previously noted that pre-existing HBoV2 immunity in a subsequent HBoV1 infection typically resulted in low or non-existent HBoV1-specific antibody responses. A phenomenon describing such immunological events among related viruses has been known since the 1950s as 'original antigenic sin' (OAS). The aim of this study was to characterize this putative OAS phenomenon in a more controlled setting. Follow-up sera of 10 rabbit pairs, inoculated twice with HBoV1-4 virus-like particles (VLPs) or control antigens, in various combinations, were analysed with HBoV1-4 IgG enzyme immunoassays with and without depletion of heterotypic HBoV antibodies. There were no significant IgG boosts after the second inoculation in either the heterologously or the homologously HBoV-inoculated rabbits, but a clear increase in cross-reactivity was seen with time. We could, however, distinguish a distinct OAS pattern from plain cross-reactivity: half of the heterologously inoculated rabbits showed IgG patterns representative of the OAS hypothesis, in line with our prior results with naturally infected children. HBoVs are the first parvoviruses to show the possible existence of OAS. Our findings provide new information on HBoV1-4 immunity and emphasize the complexity of human bocavirus diagnosis.
人博卡病毒(HBoV)1是一种广泛传播的细小病毒,可导致幼儿急性呼吸道疾病。相比之下,HBoV2出现在胃肠道,可能与肠胃炎有关,而HBoV3和 -4感染较少见,尚未与人类疾病相关联。由于HBoV1 DNA在鼻咽部持续存在,血清学被认为是诊断急性感染的更好选择。在体质健康的儿童中,我们之前注意到,在随后的HBoV1感染中,预先存在的HBoV2免疫力通常导致HBoV1特异性抗体反应较低或不存在。自20世纪50年代以来,描述相关病毒之间这种免疫事件的现象被称为“原始抗原罪”(OAS)。本研究的目的是在更可控的环境中表征这种假定的OAS现象。用HBoV1 - 4 IgG酶免疫测定法分析了10对兔子的随访血清,这些兔子以各种组合两次接种HBoV1 - 4病毒样颗粒(VLP)或对照抗原,有或没有去除异型HBoV抗体。在异源或同源HBoV接种的兔子中,第二次接种后均未出现明显的IgG增强,但随着时间的推移,交叉反应性明显增加。然而,我们可以将明显的OAS模式与单纯的交叉反应性区分开来:一半的异源接种兔子显示出代表OAS假说的IgG模式,这与我们之前对自然感染儿童的研究结果一致。HBoV是首批显示可能存在OAS的细小病毒。我们的研究结果提供了关于HBoV1 - 4免疫的新信息,并强调了人博卡病毒诊断的复杂性。