Dave V P, Hetherington S V, Portner A, Leggiadro R J, Hurwitz J L
Department of Immunology, St. Jude Children's Research Hospital, Tennessee, USA.
Virus Genes. 1997;14(2):153-6. doi: 10.1023/a:1007973402749.
Parainfluenza viruses (PIV) have been categorized into four discrete types (types 1-4), based on antigenic similarities. Here is described an evaluation of nucleoprotein (NP) sequence variability among nine patients infected with the type 1 virus. The examination of short segments of the NP sequence was sufficient to define significant variability both within and between patient samples. These data, in conjunction with previous studies of hemagglutinin-neuraminidase and fusion protein sequences from PIV-infected patient populations suggest a lack of absolute stability among isolates within each virus type. Potentially, antigenic variability exists to the extent that an immune response elicited toward one isolate may not be fully protective against another of the same type. Thus, sequence variability could contribute to natural re-infections with PIV, as well as to previous vaccine failures. Results highlight the importance of analyzing viruses that break through vaccine-induced immunity, in order to measure the influence of virus diversity on PIV vaccine outcome.
副流感病毒(PIV)根据抗原相似性已被分为四种不同类型(1-4型)。本文描述了对9名感染1型病毒患者的核蛋白(NP)序列变异性的评估。对NP序列短片段的检测足以确定患者样本内部和之间的显著变异性。这些数据,结合先前对PIV感染患者群体的血凝素神经氨酸酶和融合蛋白序列的研究,表明每种病毒类型内的分离株之间缺乏绝对稳定性。潜在地,抗原变异性的存在使得针对一种分离株引发的免疫反应可能无法完全保护机体免受同一类型另一种分离株的侵害。因此,序列变异性可能导致PIV的自然再感染以及先前疫苗接种的失败。结果强调了分析突破疫苗诱导免疫的病毒的重要性,以便衡量病毒多样性对PIV疫苗效果的影响。