Murphy B R, Graham B S, Prince G A, Walsh E E, Chanock R M, Karzon D T, Wright P F
J Clin Microbiol. 1986 Jun;23(6):1009-14. doi: 10.1128/jcm.23.6.1009-1014.1986.
An enzyme-linked immunosorbent assay (ELISA) with immunoaffinity-purified fusion (F) or attachment (G) glycoprotein was used to measure the serum and secretory immune responses of 18 infants and children, 4 to 21 months of age, who underwent primary infection with respiratory syncytial virus (RSV). Most of the 10 older individuals (9 to 21 months of age) developed moderate levels of serum and nasal-wash immunoglobin A (IgA) and IgG F and G antibodies. These individuals developed a moderate level of serum or nasal-wash antibodies that neutralized virus infectivity. One of the eight younger individuals (4 to 8 months of age) failed to develop an F antibody response, while three failed to develop a G antibody response. The most notable difference in the responses of the two age groups involved the titer in convalescent sera of G, F, and neutralizing antibodies which were 8- to 10-fold lower in younger individuals. Most of the younger infants failed to develop a rise in serum or nasal-wash neutralizing antibody. It is possible that the presence of maternally derived antibody in the younger infants suppressed the immune response to RSV infection, and that this accounted, in part, for the low level of postinfection antibody titer in this group. This low level and the irregular response of the infants less than 8 months of age may contribute to the severity of their initial infection and may also be responsible, in part, for their failure to develop effective resistance to subsequent reinfection by RSV.
采用酶联免疫吸附测定法(ELISA),以免疫亲和纯化的融合(F)糖蛋白或附着(G)糖蛋白来检测18名4至21个月大的婴幼儿的血清和分泌免疫反应,这些婴幼儿曾初次感染呼吸道合胞病毒(RSV)。10名年龄较大的个体(9至21个月大)中的大多数产生了中等水平的血清和鼻腔灌洗免疫球蛋白A(IgA)以及IgG F和G抗体。这些个体产生了能中和病毒感染性的中等水平的血清或鼻腔灌洗抗体。8名年龄较小的个体(4至8个月大)中有1名未产生F抗体反应,3名未产生G抗体反应。两个年龄组反应中最显著的差异在于恢复期血清中G、F和中和抗体的滴度,年龄较小的个体中这些抗体的滴度低8至10倍。大多数年龄较小的婴儿血清或鼻腔灌洗中和抗体未出现升高。年龄较小的婴儿中存在母源抗体可能抑制了对RSV感染的免疫反应,这在一定程度上解释了该组感染后抗体滴度较低的原因。8个月以下婴儿的这种低水平和不规则反应可能导致其初次感染的严重程度增加,也可能在一定程度上导致他们无法对随后的RSV再感染产生有效的抵抗力。