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[抗CD10母胎同种免疫]

[Anti-CD10 fetomaternal alloimmunisation].

作者信息

Ronco Pierre, Debiec Hanna, Guigonis Vincent

机构信息

Unité Inserm UMR S 702, UPMC Université Paris 6, Assistance Publique-Hôpitaux de Paris, Hôpital Tenon, Paris, France.

出版信息

Med Sci (Paris). 2009 Jan;25(1):64-8. doi: 10.1051/medsci/200925164.

Abstract

Fetomaternal alloimmunization with antenatal glomerulopathies (FMAIG) is a recently described alloimmune disorder, which results from the production of maternal antibodies that cross the placenta, bind to fetal glomerular podocytes, and mediate renal disease. The pathogenic antibodies are directed against CD10/neutral endopeptidase (NEP). The infant's mother is NEP-deficient and thus she becomes immunized during the first pregnancy against CD10/NEP expressed by placental cells. Because future pregnancies in CD10/NEP-immunized mothers are at high risk for the fetus, detection of anti-NEP antibodies in pregnant mothers and antigen-driven therapies including induction of tolerance, are urgently needed. This ideally requires identification of the pathogenic epitopes born by the antigen and specifically recognized by B- and T-cells. We have recently characterized such epitopes that will be used in diagnostic tests (ELISA) and for new therapeutic approaches based on peptide-specific immune intervention. For this purpose, we have developed an experimental model by crossing NEP/CD10-deficient female mice to wild-type males. The females develop an alloimmune reaction against NEP, which is a prerequisite for tolerance induction experiments. Although NEP/CD10 does not seem to be involved in common idiopathic forms of membranous nephropathy in the adult, alloimmune antibodies may be implicated in de novo membranous nephropathy that develop in the kidney graft and after alloimmune bone marrow transplantation.

摘要

胎儿-母体同种免疫伴发产前肾小球病(FMAIG)是一种最近描述的同种免疫性疾病,它是由母体产生的抗体穿过胎盘、与胎儿肾小球足细胞结合并介导肾脏疾病引起的。致病性抗体针对CD10/中性内肽酶(NEP)。婴儿的母亲缺乏NEP,因此她在首次怀孕时针对胎盘细胞表达的CD10/NEP产生免疫。由于CD10/NEP免疫的母亲未来怀孕时胎儿面临高风险,因此迫切需要检测孕妇体内的抗NEP抗体以及包括诱导耐受在内的抗原驱动疗法。这理想情况下需要鉴定抗原所携带的、被B细胞和T细胞特异性识别的致病表位。我们最近已鉴定出此类表位,将用于诊断测试(ELISA)以及基于肽特异性免疫干预的新治疗方法。为此,我们通过将NEP/CD10缺陷雌性小鼠与野生型雄性小鼠杂交建立了一个实验模型。雌性小鼠会针对NEP产生同种免疫反应,这是诱导耐受实验的前提条件。尽管NEP/CD10似乎不参与成人常见的特发性膜性肾病,但同种免疫抗体可能与肾移植和同种免疫骨髓移植后发生的新发膜性肾病有关。

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