Ruppel A, Diesfeld H J, Rother U
Clin Exp Immunol. 1985 Dec;62(3):499-506.
We compared the reaction in immunoblots of sera obtained from patients with parasitologically proven S. mansoni infections, with a suspected history of schistosomiasis infection, or with unrelated parasitic diseases. Several polypeptides from adult S. mansoni reacted with the schistosomiasis patients' sera in a heterogeneous manner. However, a component of approximately 31 kilo daltons (kD) reacted with all schistosomiasis sera and with several sera of suspected schistosomiasis cases. No reaction was ever observed with sera of patients harbouring other parasites. Thus, the polypeptide has potential diagnostic value. The use of sera of patients with recent infections demonstrated that: the earliest time of antibody formation against the 31 kD component was approximately 40 days post infection, the reaction with this polypeptide in immunoblots was exceptionally strong and antibodies directed against other schistosome proteins were barely detectable at this time. Identical results were obtained with sera of experimentally infected mice. The 31 kD component was present in parasites of either sex. It was apparently not a glycoprotein. Evidence suggests that the 31 kD polypeptide may originate from the schistosome gut.
我们比较了从曼氏血吸虫感染经寄生虫学证实的患者、有血吸虫病感染疑似病史的患者或患有无关寄生虫病的患者获得的血清在免疫印迹中的反应。来自曼氏血吸虫成虫的几种多肽与血吸虫病患者的血清发生了异质性反应。然而,一种约31千道尔顿(kD)的成分与所有血吸虫病血清以及一些疑似血吸虫病病例的血清发生了反应。从未观察到与感染其他寄生虫患者的血清有反应。因此,该多肽具有潜在的诊断价值。使用近期感染患者的血清表明:针对31 kD成分形成抗体的最早时间约为感染后40天,此时在免疫印迹中与该多肽的反应异常强烈,而针对其他血吸虫蛋白的抗体此时几乎检测不到。用实验感染小鼠的血清也得到了相同的结果。31 kD成分存在于雌雄两性的寄生虫中。它显然不是一种糖蛋白。有证据表明,31 kD多肽可能起源于血吸虫的肠道。