Department of Epidemiology Research, Statens Serum Institut, Copenhagen, Denmark.
Hum Immunol. 2010 Mar;71(3):263-7. doi: 10.1016/j.humimm.2010.01.006. Epub 2010 Jan 25.
Immune maladaption between mother and infant has been suggested to induce preeclampsia/eclampsia. When fetuses share more human leukocyte antigen (HLA) types with their mother, immune differences would be limited and thereby could affect this risk. Data from Danish women (1996-2002) with single live-birth pregnancies complicated by severe preeclampsia/eclampsia were compared to women with term pregnancies uncomplicated by hypertension. HLA A, B, and DR types were resolved at the intermediate-level typing (antigen). A total of 201 cases and 195 control mother-infant pairs had complete HLA types. The odds ratios of preeclampsia/eclampsia in mothers sharing both HLA antigens with their infants were 1.19 (95% confidence interval: 0.81-1.76) for HLA A, 0.91 (0.59-1.42) for HLA B, and 1.05 (0.5-1.59) for HLA DR antigens. No specific HLA antigens in either mother or infant appeared important after Bonferroni correction, except possibly DR01 in mothers (protective). Thus, maladaption mediated by adaptive immunity between mother and infant is not the basis for the mother developing preeclampsia/eclampsia.
母婴免疫失调被认为可诱发子痫前期/子痫。当胎儿与其母亲具有更多的人类白细胞抗原 (HLA) 类型时,免疫差异将受到限制,从而可能影响这种风险。对丹麦妇女(1996-2002 年)的单胎活产妊娠中严重子痫前期/子痫病例与无高血压的足月妊娠对照进行了比较。HLA A、B 和 DR 类型在中间水平(抗原)进行解析。共有 201 例病例和 195 对母婴对照具有完整的 HLA 类型。与婴儿共享 HLA 抗原的母亲发生子痫前期/子痫的比值比为 1.19(95%置信区间:0.81-1.76)对于 HLA A、0.91(0.59-1.42)对于 HLA B 和 1.05(0.5-1.59)对于 HLA DR 抗原。经过 Bonferroni 校正后,除母亲中可能的 DR01(保护)外,母亲或婴儿中没有特定的 HLA 抗原似乎很重要。因此,母婴之间适应性免疫介导的失调不是母亲发生子痫前期/子痫的基础。