Sadahiro S, Omori-Satoh T, Yamauchi K, Kondo S, Ishida S, Murata R
Jpn J Med Sci Biol. 1981 Aug;34(4):213-30. doi: 10.7883/yoken1952.34.213.
Purity of the parent toxin influenced greatly the immunogenicity in guinea pigs of HR1 component of Habu-venom toxoid. The potency of HR1 toxoid in terms of the immunizing unit (ImU) appeared to be related to the antigen and aluminum contents. The immune response of the animals differed depending on the purity of the toxoid when the dose-response curve was examined over a wide range of the antigen dosage. Anti-HR1 titers of the guinea pigs immunized with crude toxoid (adsorbed) reached a plateau at about 10-20 U/ml ane further rise was not remarkable even when the amout of the antigen was increased several times, while 200 U/ml (maximum 400 U/ml or higher) of annti-HR1 was produced with a large amount of highly purified HR1 toxoid. Purified toxoid showed an excellent immunogenicity also in monkeys. The amounts of antigens necessary for the basic immunization to resist the challenge with a certainly lethal dose of crude venom were 18 and 0.5 mg as protein, for a crude and a highly purified toxoid, respectively. The total amount of aluminum was also reduced from 8.1 (crude toxoid) to 0.5 mg (purified toxoid). Multiple injections for the primary immunization enhanced early production of anti-HR1 in monkeys. However, at later stage of immunization, significant correlation was observed between the amount of HR1 toxoid (in ImU) for the primary immunization and the circulating anti-HR1 titer irrespective of the schedule of immunization. Anti-HR2 higher than 10 U/ml was produced consistently in monkeys with HR2 toxoid of 1.0 ImU for the basic immunization. However, excess HR2 toxoid of more than 10 ImU seemed rather unfavorable for anti-HR2 production.
亲本毒素的纯度对蝮蛇毒类毒素HR1组分在豚鼠体内的免疫原性有很大影响。HR1类毒素以免疫单位(ImU)表示的效力似乎与抗原和铝含量有关。当在广泛的抗原剂量范围内检查剂量反应曲线时,动物的免疫反应因类毒素的纯度而异。用粗制类毒素(吸附型)免疫的豚鼠的抗HR1滴度在约10 - 20 U/ml时达到平台期,即使抗原量增加几倍,滴度也不会显著进一步升高,而用大量高度纯化的HR1类毒素可产生200 U/ml(最高400 U/ml或更高)的抗HR1。纯化的类毒素在猴子中也显示出优异的免疫原性。对于粗制类毒素和高度纯化的类毒素,基础免疫以抵抗一定致死剂量的粗毒液攻击所需的抗原量分别为18 mg和0.5 mg蛋白质。铝的总量也从8.1 mg(粗制类毒素)降至0.5 mg(纯化类毒素)。多次注射进行初次免疫可增强猴子体内抗HR1的早期产生。然而,在免疫后期,无论免疫方案如何,初次免疫所用HR1类毒素的量(以ImU计)与循环抗HR1滴度之间都存在显著相关性。用1.0 ImU的HR2类毒素进行基础免疫的猴子始终能产生高于10 U/ml的抗HR2。然而,超过10 ImU的过量HR2类毒素似乎对抗HR2的产生相当不利。