Lisowska-Myjak Barbara, Szczepanik Kamil, Skarżyńska Ewa, Jakimiuk Artur
Department of Biochemistry and Pharmacogenomics, Medical University of Warsaw, 02-097 Warsaw, Poland.
Department of Laboratory Medicine, Medical University of Warsaw, 02-097 Warsaw, Poland.
Int J Mol Sci. 2025 Aug 5;26(15):7579. doi: 10.3390/ijms26157579.
IgG Fc binding protein (FcGBP) is a mucin-like protein that binds strongly to IgG and IgG-antigen complexes in intestinal mucus. FcGBP presence and its altered expression levels in meconium accumulating in the fetal intestine and amniotic fluid flowing in the intestine may provide new knowledge of the mechanisms responsible for the immune adaptation of the fetus to extrauterine life. FcGBP concentrations were measured by ELISA in the first-pass meconium and amniotic fluid samples collected from 120 healthy neonates delivered by either vaginal birth ( = 35) or cesarean section ( = 85) at 36 to 41 weeks gestation. The meconium FcGBP concentrations (405.78 ± 145.22 ng/g) decreased (r = -0.241, = 0.007) over the course of 36 to 41 weeks gestation, but there were no significant changes ( > 0.05) in the amniotic fluid FcGBP (135.70 ± 35.83 ng/mL) in the same period. Both meconium and amniotic fluid FcGBP concentrations were higher ( < 0.05) in neonates delivered by cesarean section. Decreases in the meconium FcGBP concentrations correlated (r = -0.37, = 0.027) with the gestational age in neonates delivered by vaginal birth but not in those delivered by cesarean section ( > 0.05). No association was found between the FcGBP concentrations in meconium and amniotic fluid and the birth weight ( > 0.05). With the development of the mucosal immune system in the fetal intestine over the course of the third trimester of gestation, the meconium FcGBP concentrations decrease. Increased FcGBP concentrations measured in the meconium and amniotic fluid of neonates delivered by cesarean section may possibly indicate altered intestinal mucosal function. Intrauterine growth is not associated with the intestinal mucosal barrier maturation involving FcGBP.
IgG Fc结合蛋白(FcGBP)是一种黏蛋白样蛋白,它能与肠道黏液中的IgG及IgG - 抗原复合物紧密结合。胎儿肠道中积聚的胎粪以及肠道内流动的羊水中FcGBP的存在及其表达水平的改变,可能为胎儿免疫适应宫外生活的机制提供新的认识。采用酶联免疫吸附测定法(ELISA)检测了120例在妊娠36至41周时经阴道分娩(n = 35)或剖宫产(n = 85)的健康新生儿的初排胎粪和羊水样本中的FcGBP浓度。胎粪FcGBP浓度(405.78±145.22 ng/g)在妊娠36至41周期间呈下降趋势(r = -0.241,P = 0.007),但同期羊水FcGBP浓度(135.70±35.83 ng/mL)无显著变化(P>0.05)。剖宫产分娩的新生儿的胎粪和羊水FcGBP浓度均较高(P<0.05)。经阴道分娩的新生儿,胎粪FcGBP浓度的下降与胎龄相关(r = -0.37,P = 0.027),而剖宫产分娩的新生儿则无此相关性(P>0.05)。未发现胎粪和羊水中FcGBP浓度与出生体重之间存在关联(P>0.05)。随着妊娠晚期胎儿肠道黏膜免疫系统的发育,胎粪FcGBP浓度降低。剖宫产分娩的新生儿的胎粪和羊水中FcGBP浓度升高可能表明肠道黏膜功能发生了改变。宫内生长与涉及FcGBP的肠道黏膜屏障成熟无关。