Mason R A, Tauraso N M, Ginn R K, O'Brien T C, Trimmer R W
Appl Microbiol. 1972 May;23(5):908-13. doi: 10.1128/am.23.5.908-913.1972.
A dosage equal to or greater than approximately 3.4 Dex (decimal exponent, log(10)) weanling mouse intracerebral 50% lethal dose (LD(50)) was sufficient to elicit a yellow fever antibody response, as determined by the plaque neutralization (PN) test, in better than 90% of vaccinated rhesus monkeys. Lower dosages were progressively less effective in terms of PN titers and the PN and hemagglutination-inhibition serological conversion rates observed. A dose of between 3.4 and 4.2 Dex weanling mouse intracerebral LD(50), or one-tenth to one times the dosage recommended for man, provided an optimal antibody response in monkeys. In rhesus monkeys, in contrast to the findings for man, pre-existing yellow fever antibody did not interfere with the antibody response to yellow fever vaccine. The PN test was felt to be a more sensitive and specific indicator of yellow fever antibody in rhesus monkeys after vaccination than the hemagglutination inhibition or complement fixation tests.
通过空斑中和(PN)试验测定,等于或大于约3.4 Dex(十进制指数,log(10))断奶小鼠脑内50%致死剂量(LD(50))的剂量足以在超过90%的接种恒河猴中引发黄热病抗体反应。就观察到的PN滴度以及PN和血凝抑制血清转化率而言,较低剂量的效果逐渐降低。3.4至4.2 Dex断奶小鼠脑内LD(50)的剂量,即推荐给人类剂量的十分之一至一倍,能使猴子产生最佳抗体反应。与人类的研究结果相反,在恒河猴中,预先存在的黄热病抗体并不干扰对黄热病疫苗的抗体反应。人们认为,PN试验比血凝抑制或补体结合试验更能灵敏且特异地指示接种后恒河猴体内的黄热病抗体。