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预防早产:基于微生物与宿主相互作用的新举措。

Prevention of preterm birth: new initiatives based on microbial-host interactions.

作者信息

McGregor J A

机构信息

Department of Obstetrics and Gynecology, University of Colorado Health Sciences Center, Denver 80220.

出版信息

Obstet Gynecol Surv. 1988 Jan;43(1):1-14.

PMID:3277101
Abstract

Preterm delivery remains a preeminent problem in reproductive and pediatric care worldwide. Recent data suggest that cervicovaginal microflora and/or the inflammatory response they engender produce factors which can cause or predispose to preterm labor and rupture of membranes. Microorganisms mediating such processes may not be "recognized pathogens" and are often considered normal flora. These microorganisms may act singly, additively, or synergistically with host factors released during an induced inflammatory response. Quantitative, as well as qualitative aspects of cervicovaginal microflora may be important. Multiple cervicovaginal microorganisms produce IgA protease, neuraminidase, and mucinase which may facilitate passage of these and other agents past cervical barriers and into the lower uterine segment. Multiple microflora also produce phospholipases A2 and C, each of which can locally augment production of eicosanoids within the uterus which are important in cervical ripening and labor. Similar microflora produce various proteases, including collagenase, which can focally weaken the amniochorion and predispose to premature rupture of membranes and cervical ripening. Intrauterine microorganisms induce inflammatory reaction and may engender local release of similar proteases, phospholipases, as well as platelet-activating factor (PAF) and lymphokines which can also initiate or further potentiate labor-inducing mechanisms. Recognition of microbe-induced pathogenesis of some cases of preterm birth offers the hope of specific treatment and prophylaxis. In recent studies, administration of erythromycin and tocolytic agents was associated with an improved outcome in selected women with preterm labor. Further microbiological and clinical studies are ongoing. "Just why so many gravidas go into labor prematurely and hence give birth to infants who often are unable to cope with extrauterine conditions is one of the great unsolved problems of obstetrics."

摘要

早产仍然是全球生殖和儿科护理领域的一个突出问题。最近的数据表明,宫颈阴道微生物群和/或它们引发的炎症反应会产生一些因素,这些因素可导致早产和胎膜破裂,或使个体更易发生早产和胎膜破裂。介导此类过程的微生物可能并非“公认的病原体”,通常被视为正常菌群。这些微生物可能单独起作用,也可能与诱导炎症反应期间释放的宿主因素相加或协同起作用。宫颈阴道微生物群的定量和定性方面可能都很重要。多种宫颈阴道微生物会产生IgA蛋白酶、神经氨酸酶和粘蛋白酶,这些酶可能有助于这些病原体及其他病原体穿过宫颈屏障并进入子宫下段。多种微生物还会产生磷脂酶A2和C,它们均可在局部增加子宫内类花生酸的生成,而类花生酸在宫颈成熟和分娩过程中起着重要作用。类似的微生物会产生多种蛋白酶,包括胶原酶,这些酶可局部削弱羊膜绒毛膜,导致胎膜早破和宫颈成熟。子宫内的微生物会引发炎症反应,并可能导致局部释放类似的蛋白酶、磷脂酶,以及血小板激活因子(PAF)和淋巴因子,这些物质也可启动或进一步增强引产机制。认识到微生物诱导某些早产病例的发病机制,为特异性治疗和预防带来了希望。在最近的研究中,对某些早产女性使用红霉素和解痉剂与改善结局相关。进一步的微生物学和临床研究正在进行中。“为何如此多的孕妇会过早分娩,从而生下往往无法适应宫外环境的婴儿,这是产科领域一个重大的未解之谜。”

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