Lachmann P J, Lay E, Seilly D J, Buchberger A, Schwaeble W, Khadake J
Department of Veterinary Medicine, University of Cambridge, Cambridge, UK.
Department of Infection, Immunity and Inflammation, University of Leicester, Leicester, UK.
Clin Exp Immunol. 2016 Jan;183(1):150-6. doi: 10.1111/cei.12714. Epub 2015 Nov 5.
In this paper we have extended our earlier studies of the action of increasing Factor I concentration on complement activation by using a soluble activator, lipopolysaccharide (LPS) endotoxin, and using human erythrocytes as a source of CR1 - the co-factor needed for the final clip of iC3b to C3dg by Factor I. Using this more physiological system, the results show that we can predict that a quite modest increase in Factor I concentration - 22 µg/ml of extra Factor I - will convert the activity of the highest risk sera to those of the lowest risk. Preliminary experiments have been performed with erythrocytes allotyped for CR1 number. While we have not been able to perform an adequate study of their co-factor activities in our assays, preliminary experiments suggest that when Factor I levels are increased the difference produced by different allotypes of red cells is largely overcome. This suggests that in patients with paroxysmal nocturnal haemoglobinuria (PNH) treated with eculizumab, additional treatment with Factor I may be very useful in reducing the need for blood transfusion. We have also explored the age-related allele frequency for the two polymorphisms of Factor H and the polymorphism of C3. In our population, unlike the 1975 study, we found no age variation in the allele frequency in these polymorphisms. This may, however, reflect that the Cambridge BioResource volunteers do not include many very young or very elderly patients, and in general comprise a population not greatly at risk of death from infectious disease.
在本文中,我们扩展了早期关于增加因子I浓度对补体激活作用的研究,采用了可溶性激活剂脂多糖(LPS)内毒素,并使用人类红细胞作为CR1的来源,CR1是因子I将iC3b最终裂解为C3dg所需的辅助因子。使用这个更接近生理状态的系统,结果表明我们可以预测,因子I浓度相当适度的增加——额外添加22μg/ml的因子I——将把最高风险血清的活性转变为最低风险血清的活性。我们已经对具有不同CR1数量血型的红细胞进行了初步实验。虽然我们还无法在我们的检测中对它们的辅助因子活性进行充分研究,但初步实验表明,当因子I水平升高时,不同血型红细胞产生的差异在很大程度上会被克服。这表明,对于接受依库珠单抗治疗的阵发性夜间血红蛋白尿(PNH)患者,额外使用因子I治疗可能对减少输血需求非常有用。我们还研究了因子H的两种多态性和C3多态性的年龄相关等位基因频率。在我们的人群中,与1975年的研究不同,我们发现这些多态性的等位基因频率没有年龄差异。然而,这可能反映出剑桥生物资源志愿者中没有很多非常年轻或非常年长的患者,总体上构成的人群因传染病死亡的风险不大。