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补体系统的动力学及其临床意义,特别是与正常人类妊娠、分娩、产褥期及胎儿相关的替代途径(作者译)

[The dynamics and its clinical significance of complement system, especially alternative pathway related to normal human pregnancy, delivery, puerperium and fetus (author's transl)].

作者信息

Ohhashi T

出版信息

Nihon Sanka Fujinka Gakkai Zasshi. 1980 Jan;32(1):27-36.

PMID:6909273
Abstract

The author studied human complement system, especially alternative pathway as a primitive biological defense system, in maternal serum during normal pregnancy, delivery and puerperium. The results obtained were as follows. 1. The mean value of hemolytic activity of alternative pathway (AlCH50) in healthy women was 18.3 +/- 1.1. This value was increased gradually in progress of gestational stages up to 26.6 +/- 2.3 of the average in the last trimester. Stochastically, significant differences about this value was noted between in the first trimester and in the last. This AlCH50 is decreased temporarily at delivery, and it was increased again rapidly, then went down to normal range about one month after delivery. 2. The average of immunochemical C3PA by SRID method during pregnancy was 22.5 +/- 0.4 mg/dl. It was significantly higher than the average 18.1 +/- 0.4 mg/dl of 59 healthy women. C3PA was noted to remain high level constantly during pregnancy. This C3PA level after delivery was observed to take a similar pattern as AlCH50. 3. beta 1C/1A globulin (C3) in 19 healthy women was 60.7 +/- 2.1 mg/dl. This C3 was also increased gradually during pregnancy up to maximum level of 87.5 +/- 2.8 mg/dl at the 3rd trimester. 4. Classical pathway (CH50, C4 and Cl INA) and fetal complement level were investigated at the same time and discussed here.

摘要

作者研究了正常妊娠、分娩及产褥期母体血清中的人类补体系统,尤其是作为一种原始生物防御系统的替代途径。获得的结果如下。1. 健康女性替代途径溶血活性(AlCH50)的平均值为18.3±1.1。该值在妊娠各阶段逐渐升高,直至妊娠晚期平均达到26.6±2.3。随机分析显示,该值在妊娠早期和晚期之间存在显著差异。AlCH50在分娩时暂时降低,然后迅速再次升高,产后约一个月降至正常范围。2. 妊娠期间通过单向免疫扩散法测得的免疫化学C3PA平均值为22.5±0.4mg/dl。显著高于59名健康女性的平均值18.1±0.4mg/dl。C3PA在妊娠期间持续保持高水平。观察到产后C3PA水平与AlCH50呈现相似模式。3. 19名健康女性的β1C/1A球蛋白(C3)为60.7±2.1mg/dl。该C3在妊娠期间也逐渐升高,在妊娠晚期达到最高水平87.5±2.8mg/dl。4. 同时对经典途径(CH50、C4和Cl INA)和胎儿补体水平进行了研究并在此讨论。

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