Bickle Q D
Parasitology. 1982 Feb;84(1):111-22. doi: 10.1017/s0031182000051702.
These studies were aimed at giving a clearer idea of the source of the antigens responsible for the induction of resistance by larval schistosomes. Firstly, the resistance induced by radiation-attenuated (20 krad.) infections was compared with that induced by the larval phase of unirradiated infections. The superiority of the irradiated larvae was demonstrated by infecting mice with 500 female cercariae which were either unirradiated or irradiated, and challenging them 3 weeks later with male cercariae. At perfusion, when primary and challenge worms could be distinguished by sex, significantly greater resistance was demonstrated in the groups vaccinated with irradiated larvae (56 cf. 31% and 48 cf. 26% in two experiments). Secondly, in order to establish how long immunizing larvae need to survive to stimulate optimum resistance, mice were either treated with schistosomulicidal drugs or had the site of infection excised at various intervals post-vaccination. Treatment or excision at up to 24 h did not result in significant resistance to challenge (6-16%). Similar treatments at 1 week did not prevent significant resistance developing (26-37%) but the levels of resistance were significantly lower than those manifest by vaccinated, untreated mice (51-71%). It is concluded that the immunizing larvae need to persist for between 1 and 2 weeks in order to stimulate optimum protection and that antigens released during protracted survival and/or death of the larvae in either the skin or the lungs are probably key factors in the induction of resistance.
这些研究旨在更清楚地了解导致幼虫期血吸虫诱导抗性的抗原来源。首先,将辐射减毒(20千拉德)感染诱导的抗性与未辐射感染的幼虫期诱导的抗性进行比较。通过用500只未辐射或已辐射的雌性尾蚴感染小鼠,并在3周后用雄性尾蚴对其进行攻击,证明了辐射幼虫的优越性。在灌注时,当原发和攻击蠕虫可以按性别区分时,接种辐射幼虫的组表现出显著更高的抗性(在两个实验中分别为56%对31%和48%对26%)。其次,为了确定免疫幼虫需要存活多长时间才能刺激最佳抗性,在接种疫苗后的不同时间间隔,用杀血吸虫药物处理小鼠或切除感染部位。在接种后长达24小时进行处理或切除,对攻击没有产生显著抗性(6 - 16%)。在1周时进行类似处理并不能阻止显著抗性的发展(26 - 37%),但抗性水平显著低于未处理的接种疫苗小鼠所表现出的水平(51 - 71%)。得出的结论是,免疫幼虫需要持续1至2周才能刺激最佳保护,并且幼虫在皮肤或肺部长期存活和/或死亡期间释放的抗原可能是诱导抗性的关键因素。