Scott Paul D, Ochola Rachel, Sande Charles, Ngama Mwanajuma, Okiro Emelda A, Medley Graham F, Nokes D James, Cane Patricia A
Department of Biological Sciences, University of Warwick, Coventry, UK.
J Med Virol. 2007 Dec;79(12):1943-50. doi: 10.1002/jmv.20999.
Respiratory syncytial virus (RSV) is a major cause of lower respiratory tract infection in infants. RSV repeatedly reinfects individuals: this may be due in part to the variability of the attachment (G) glycoprotein and changes in this protein have been shown to be under positive selection. Infants experiencing their primary infection show a genotype-specific antibody response with respect to the variable regions of the G protein. A prospective study of RSV infections in a birth cohort in rural Kenya identified infants experiencing repeat infections with RSV. The serum antibody responses of these infants were investigated with respect to their anti-RSV reactions in an enzyme-linked immunosorbent assay (ELISA) and the specificity of the response to a variable region of the G protein by ELISA and immunoblotting using bacterially expressed polypeptides representative of the currently circulating strains of RSV. The results presented here confirm that the primary antibody response to the variable regions of the G protein is generally genotype-specific, but show that the response may become cross-reactive (at least within group A viruses) during secondary infections even where the secondary infection is of the same genotype as the initial infection. Also, some infants who did not mount a detectable antibody response to whole RSV antigens during their primary infection nevertheless showed genotype-specific responses to the G protein. In conclusion, the strain-specific nature of the serum antibody response to the variable regions of the G protein of RSV observed in primary infections can become cross-reactive in subsequent reinfections.
呼吸道合胞病毒(RSV)是婴儿下呼吸道感染的主要病因。RSV会反复感染个体:这可能部分归因于附着(G)糖蛋白的变异性,且已表明该蛋白的变化处于正选择之下。经历初次感染的婴儿对G蛋白可变区表现出基因型特异性抗体反应。一项对肯尼亚农村出生队列中RSV感染的前瞻性研究确定了经历RSV反复感染的婴儿。通过酶联免疫吸附测定(ELISA)研究了这些婴儿的血清抗体反应,以了解其抗RSV反应,并通过ELISA以及使用代表当前流行的RSV毒株的细菌表达多肽进行免疫印迹,研究了对G蛋白可变区反应的特异性。此处呈现的结果证实,对G蛋白可变区的初次抗体反应通常具有基因型特异性,但表明在二次感染期间,即使二次感染与初次感染的基因型相同,该反应也可能变得具有交叉反应性(至少在A组病毒内)。此外,一些在初次感染期间对整个RSV抗原未产生可检测抗体反应的婴儿,对G蛋白仍表现出基因型特异性反应。总之,在初次感染中观察到的对RSV G蛋白可变区血清抗体反应的毒株特异性性质,在随后的再次感染中可能会变得具有交叉反应性。