Santoro F, Ouaissi M A, Pestel J, Capron A
J Immunol. 1980 Jun;124(6):2886-91.
In earlier studies we have found that activation of the classical complement pathway (CCP) by the immature schistosomes involves the presence of IgG. By investigating the first step of this activation we have demonstrated in the present work that binding of C1q to schistosomula can occur by two different routes: 1) directly, by specific C1q receptors, and 2) indirectly through the IgG previously attached to Fc receptors present on the parasite surface. Only this second mechanism appears to be involved in CCP activation by schistosomula. Moreover, certain low m.w. schistosome antigens (less than 20,000), which activate CCP, also directly fixed C1q. In this case, IgG are not required for C activation. The presence of receptors for host protein, essentially in 2- to 3-hr-old schistosomula, i.e., the life stage of Schistosoma mansoni that are first in contact with the host, could be the first mechanism by which the schistosomes evade the immune attack.
在早期研究中,我们发现未成熟血吸虫激活经典补体途径(CCP)涉及IgG的存在。通过研究这种激活的第一步,我们在本研究中证明,C1q与童虫的结合可通过两种不同途径发生:1)直接通过特异性C1q受体,2)间接通过先前附着在寄生虫表面Fc受体上的IgG。似乎只有这第二种机制参与童虫对CCP的激活。此外,某些激活CCP的低分子量血吸虫抗原(小于20,000)也直接结合C1q。在这种情况下,补体激活不需要IgG。宿主蛋白受体主要存在于2至3小时龄的童虫中,即曼氏血吸虫最先与宿主接触的生命阶段,这可能是血吸虫逃避免疫攻击的首要机制。