Offit P A, Clark H F, Plotkin S A
Infect Immun. 1983 Oct;42(1):293-300. doi: 10.1128/iai.42.1.293-300.1983.
Sera from (i) gnotobiotic BALB/c, CD-1, and CFW mice and (ii) conventional BALB/c mice were evaluated by radioimmunoassay, radioimmunoprecipitation, and plaque reduction neutralization, using the Wa, SA-11, and WC-3 (bovine) strains of rotavirus as the detecting antigens. The gnotobiotic mice had no antirotavirus antibody detectable by radioimmunoprecipitation and no neutralizing antibody at a dilution of 1:50 by plaque reduction neutralization. All sera from the conventional mice had rotavirus-specific antibodies detected by radioimmunoassay and by radioimmunoprecipitation at serum dilutions of 1:50 and 1:10,000, respectively. The antibodies were directed against viral proteins p116, p94, p88, and p84 of all three viruses, but had no neutralizing activity against heterologous rotaviruses at a dilution of 1:50. Conventional seropositive mice were parenterally immunized with the Wa, SA-11, or WC-3 strain of rotavirus. An approximate 100-fold increase in rotavirus-specific antibodies was detected by radioimmunoassay, and greater than 20-fold selective neutralization of the immunizing strain of virus was observed. Sera from the mice immunized with Wa virus had antibodies directed against inner and outer capsid proteins of all three rotaviruses. The mouse can be a useful model for studying the immune response to heterologous rotavirus infection; preexisting antibodies presumably directed towards murine rotavirus do not prevent the development of a type-specific immune response to a nonmurine rotavirus.
使用轮状病毒的Wa、SA - 11和WC - 3(牛)株作为检测抗原,通过放射免疫测定、放射免疫沉淀和蚀斑减少中和试验,对(i)无菌BALB/c、CD - 1和CFW小鼠以及(ii)普通BALB/c小鼠的血清进行了评估。无菌小鼠通过放射免疫沉淀法检测不到抗轮状病毒抗体,通过蚀斑减少中和试验在1:50稀释度下也没有中和抗体。所有普通小鼠的血清在血清稀释度分别为1:50和1:10,000时,通过放射免疫测定和放射免疫沉淀法检测到有轮状病毒特异性抗体。这些抗体针对所有三种病毒的病毒蛋白p116、p94、p88和p84,但在1:50稀释度下对异源轮状病毒没有中和活性。对普通血清阳性小鼠进行了Wa、SA - 11或WC - 3株轮状病毒的非肠道免疫。通过放射免疫测定检测到轮状病毒特异性抗体增加了约100倍,并且观察到对免疫病毒株的选择性中和作用增加了20倍以上。用Wa病毒免疫的小鼠血清中含有针对所有三种轮状病毒的内壳和外壳蛋白的抗体。小鼠可以作为研究对异源轮状病毒感染免疫反应的有用模型;预先存在的可能针对鼠轮状病毒的抗体并不能阻止对非鼠轮状病毒产生型特异性免疫反应。