Schettini Juliana Araújo de Carvalho, Gomes Thomás Virgílio, Santos Barreto Alexandra Karla, da Silva Júnior Claudeir Dias, da Matta Marina, Coutinho Isabela Cristina Neiva, de Oliveira Maria do Carmo Valgueiro Costa, Torres Leuridan Cavalcante
Translational Research Laboratory, Instituto de Medicina Integral Prof. Fernando Figueira (IMIP), Recife, Brazil.
Department of Obstetrics and Gynecology, Instituto de Medicina Integral Prof. Fernando Figueira (IMIP), Recife, Brazil.
Front Immunol. 2017 Jul 3;8:700. doi: 10.3389/fimmu.2017.00700. eCollection 2017.
Maternal RhD alloimmunization is an inflammatory response against protein antigens in fetal red blood cells (RBC). However, not all women become alloimmunized when exposed to RhD fetal RBC. Thus, this study aimed to evaluate levels of inflammatory chemokines in RhD pregnant women with erythrocyte alloimmunization. CXCL8, CXCL9, CCL5, and CXCL10 levels were determined from cell culture supernatants by flow cytometry in 46 (30 non-alloimmunized RhD and 16 previously alloimmunized RhD) pregnant women. CXCL8 levels were significantly higher ( < 0.004), and CXCL9 ( < 0.008) and CXCL10 ( < 0.003) levels were significantly lower in alloimmunized pregnant women. No significant difference in CCL5 levels was detected between the groups. Fetal RHD genotyping was performed in the alloimmunized RhD group by real-time PCR. Anti-D alloantibody was detected in 10 mothers and anti-D and -C in six mothers. Twelve fetuses were RHD positive and four were RHD negative. Further studies of serum chemokines and placenta tissue could provide a better understanding of the cells involved in the pathogenesis of maternal erythrocyte alloimmunization.
母源性RhD同种免疫是针对胎儿红细胞(RBC)中蛋白质抗原的一种炎症反应。然而,并非所有接触RhD胎儿红细胞的女性都会发生同种免疫。因此,本研究旨在评估发生红细胞同种免疫的RhD孕妇体内炎症趋化因子的水平。通过流式细胞术测定了46名(30名未发生同种免疫的RhD孕妇和16名既往发生过同种免疫的RhD孕妇)孕妇细胞培养上清液中CXCL8、CXCL9、CCL5和CXCL10的水平。在发生同种免疫的孕妇中,CXCL8水平显著升高(<0.004),而CXCL9(<0.008)和CXCL10(<0.003)水平显著降低。两组之间CCL5水平未检测到显著差异。通过实时PCR对发生同种免疫的RhD组进行胎儿RHD基因分型。在10名母亲中检测到抗-D同种抗体,在6名母亲中检测到抗-D和抗-C。12名胎儿RHD呈阳性,4名胎儿RHD呈阴性。对血清趋化因子和胎盘组织的进一步研究可能有助于更好地了解参与母源性红细胞同种免疫发病机制的细胞。