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衰变加速因子(DAF)作为对血吸虫童虫补体杀伤具有保护活性的宿主抗原。

Decay accelerating factor (DAF) as the host antigen with protective activity to complement killing of schistosomula.

作者信息

Ramalho-Pinto F J

机构信息

Departamento de Bioquímica e Immunologia, ICB, UFMG, Belo Horizonte, MG, Brasil.

出版信息

Mem Inst Oswaldo Cruz. 1987;82 Suppl 4:213-6. doi: 10.1590/s0074-02761987000800037.

Abstract

The acquisition of host antigens by Schistosoma mansoni was studied by evaluating the resistance of schistosomula to the complement attack mediated by lethal antibody. Schistosomula cultured for 24 hours with intact human erythrocytes (N-HuE) or ghosts of any type of ABO or Rh blood group, showed a marked resistance to complement damage. Sheep red blood cells, pronase-treated N-HuE or erythrocytes from patients with paroxysmal nocturnal hemoglobinuria, which are complement-sensitive cells, were unable to protect schistosomula. Schistosomula protected by N-HuE became again susceptible to complement killing after incubation with a monoclonal antibody anti-DAF. These results indicate that, in vitro, host DAF from N-HuE can be acquired by schistosomula surface in a biological active form that protects the parasite from the complement lesion.

摘要

通过评估血吸虫幼虫对致死性抗体介导的补体攻击的抗性,研究了曼氏血吸虫对宿主抗原的获取情况。用完整的人红细胞(N-HuE)或任何ABO或Rh血型的血影培养24小时的血吸虫幼虫,对补体损伤表现出显著抗性。绵羊红细胞、经链霉蛋白酶处理的N-HuE或阵发性夜间血红蛋白尿患者的红细胞,这些都是补体敏感细胞,无法保护血吸虫幼虫。经N-HuE保护的血吸虫幼虫在与抗衰变加速因子(DAF)单克隆抗体孵育后,再次变得易受补体杀伤。这些结果表明,在体外,来自N-HuE的宿主DAF可以以生物活性形式被血吸虫幼虫表面获取,从而保护寄生虫免受补体损伤。

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