Späth P J, Braun M, Meyer-Hänni L, Mohren D, Mauff G
Zentrallaboratorium Blutspendedienst, SRK, Bern, Schweiz.
Vox Sang. 1990;59 Suppl 1:51-8. doi: 10.1111/j.1423-0410.1990.tb01643.x.
The complement system, as the effector mechanism of the antigen-antibody reaction, and the levels of circulating immune complexes in a 1-year, double-blind, randomized, placebo-controlled study served as laboratory parameters to assess the effect of long-term high-dose intravenous immunoglobulin (IVIG) therapy in 30 adult patients (2 x 15) with AIDS-related complex/Walter-Reed 5 (ARC/WR5). We obtained no evidence of an adverse effect in such patients of high-dose IVIG administered over a 6-month period: none of the parameters studied showed a significant difference between the two groups of patients. In both groups, using data before the first infusion or using data of the whole study, a correlation between circulating immune complexes and classical complement pathway activation was found. The most striking increase was seen in the two groups of patients for functional serum factor D. The accumulation of serum factor D was not paralleled by an increase in serum creatinine. In patients with disease progressing from ARC to AIDS within the study period, an accumulation of serum factor D was not more or less pronounced than in those who remained in the ARC stage. Accumulation of factor D was not related to the clinical score as assessed in this study.
补体系统作为抗原抗体反应的效应机制,在一项为期1年的双盲、随机、安慰剂对照研究中,循环免疫复合物水平作为实验室参数,用于评估30例成人艾滋病相关综合征/沃尔特·里德5型(ARC/WR5)患者长期大剂量静脉注射免疫球蛋白(IVIG)治疗的效果。我们没有获得在6个月期间给予此类患者大剂量IVIG有不良反应的证据:研究的参数在两组患者之间均未显示出显著差异。在两组中,无论是使用首次输注前的数据还是整个研究的数据,均发现循环免疫复合物与经典补体途径激活之间存在相关性。两组患者中功能性血清因子D的增加最为显著。血清因子D的积累并未伴随血清肌酐的升高。在研究期间疾病从ARC进展为艾滋病的患者中,血清因子D的积累与仍处于ARC阶段的患者相比,并无更明显或更不明显的情况。因子D的积累与本研究评估的临床评分无关。