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Abstract
Purpose of research – determine the relationship of serum markers of fetoplacental barrier permeability in the blood and amniotic fluid of pregnant women with premature rupture of the fetal membranes to identify non-selective permeability in VUI in newborns.
Materials and methods. 63 pregnant women with premature rupture of the fetal membranes (PRPO) at 24-33 weeks were examined. 35 women had children without signs of VUI; 28 had severe VUI (early neonatal sepsis, spilled herpes, Chlamydia and Candida infections, pneumonia and meningitis).
The content of alpha-2-macroglobulin (α2-MG) in the serum of pregnant women and umbilical cord serum (PS) was determined by quantitative rocket immunoelectrophoresis, in amniotic fluid (OV) – by ELISA, the concentration of albumin (ALB) in SB and PS – by biochemical method, in OV – by quantitative rocket immunoelectrophoresis. Statistical analysis was performed using logistic regression.
Results. When a child is born with severe VUI in PRPO, there is a significant increase in the concentration of high-molecular α2-MG (720 kDa) and low-molecular albumin (56 kDa) of serum origin in the amniotic fluid of women who gave birth to children without VUI. At the same time, the serum content of α2-MG in women in labor with severe VUI is sharply reduced, and albumin is comparable to the comparison group. Significant differences in the levels of the studied proteins were not found in the study of PC.
Conclusion. The low level of α2-MG (< 2.1 g/l) in blood serum on the background of increased concentrations of α2-MG (≥ 0.01 mg/l) and albumin (≥ 1.6 g/l) in S with premature rupture of membranes, indicate the presence of nonselective permeability of the fetoplacental barrier, including high molecular weight proteins and pathogens, the risk of infectious damage of the placenta and severe generalized IUI fetus and newborn.
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Burton GJ, Fowden AL. The placenta: a multifaceted, transient organ. Philos. Trans. R. Soc. Lond. B Biol. Sci. 2015; 370(1663): 20140066. doi: 10.1098/rstb.2014.0066
Chiu CF, Chu LW, Liao IC, Simanjuntak Y, Lin YL, Juan CC, Ping YH. The Mechanism of the Zika Virus Crossing the Placental Barrier and the Blood-Brain Barrier. Front Microbiol. 2020; 11: 214-228. doi: 10.3389/fmicb.2020.00214
David E, Riki L, Ariel JJ, Gernot D, Moshe H. Have We Neglected the Role of Fetal Endothelium in Transplacental Transport? Traffic. 2014; 15(1): 122-126. doi: 10.1111/tra.12130
Rubinchik-Stern M, Eyal S. Drug interactions at the human placenta: What is the evidence? Front. Pharmacol. 2012; 3: 126-132. doi: 10.3389/fphar.2012.00126
Hui P. Molecular diagnosis of gestational trophoblastic disease. Expert Rev Mol Diagn. 2010; 10(8): 1023-1034. doi: 10.1586/erm.10.93
Hui P. Gestational Trophoblastic Disease: Diagnostic and Molecular Genetic Pathology. New York: Humana Press; 2011. 205 p.
Delorme-Axford E, Sadovsky Y, Coyne CB. The Placenta as a barrier to viral infections. Annu. Rev. Virol. 2014; 1, 133-146. doi: 10.1146/annurev-virology-031413-085524
Calvet G, Aguiar RS, Melo ASO, Sampaio SA, De Filippis I, Fabri A et al. Detection and sequencing of Zika virus from amniotic fluid of fetuses with microcephaly in Brazil: a case study. Lancet Infect. Dis. 2016; 16(6): 653-660. doi: 10.1016/S1473-3099(16)00095-5
Mlakar J, Korva M, Tul N, Popovic M, Poljsak-Prijatelj M, Mraz J et al. Zika virus associated with microcephaly. N. Engl. J. Med 2016; 374(10): 951–958. doi: 10.1056/NEJMoa1600651
Coyne CB, Lazear HM. Zika virus – reigniting the TORCH. Nat. Rev. Microbiol. 2016; 14(11): 707-715. doi: 10.1038/nrmicro.2016.125
Al-Obaidi MMJ, Bahadoran A, Har LS, Mui WS, Rajarajeswaran J, Zandi K et al. Japanese encephalitis virus disrupts blood-brain barrier and modulates apoptosis proteins in THBMEC cells. Virus Res. 2017; 233: 17-28. doi: 10.1016/j.virusres.2017.02.012
Leibrand CR, Paris JJ, Ghandour MS, Knapp PE, Kim W-K, Hauser KF, McRae M. HIV-1 Tat disrupts blood-brain barrier integrity and increases phagocytic perivascular macrophages and microglia in the dorsal striatum of transgenic mice. Neurosci. Lett. 2017; 640: 136-143. doi: 10.1016/j.neulet.2016.12.073
Mittal R, Nguyen D, Debs LH, Patel AP, Liu G, Jhaveri VM et al. Zika virus: an emerging global health threat. Front. Cell Infect. Microbiol. 2017; 7: 486-503. doi: 10.3389/fcimb.2017.00486
Hewitt M, Madden JC, Rowe PH, Cronin MTD. Structure-based modeling in reproductive toxicology: (Q)SARs for the placental barrier. SAR QSAR Environ. Res. 2007; 18(1-2): 57-76. doi: 10.1080/10629360601053893
Giaginis C, Zira A, Theocharis S, Tsantili-Kakoulidou A. Application of quantitative structure-activity relationships for modeling drug and chemical transport across the human placenta barrier: A multivariate data analysis approach. J. Appl. Toxicol. 2009; 29(8): 724-733. doi: 10.1002/jat.1466
Giaginis C, Theocharis S, Tsantili-Kakoulidou A. Current toxicological aspects on drug and chemical transport and metabolism across the human placental barrier. Expert Opin. Drug Metab. Toxicol. 2012; 8(10): 1263-1275. doi: 10.1517/17425255.2012.699041
Sohn DH, Sokolove J, Sharpe O, Erhart JC, Chandra PE, Lahey LJ et al. Plasma proteins present in osteoarthritic synovial fluid can stimulate cytokine production via Toll-like receptor 4. Arthritis Res Ther. 2012; 14(1): R7-R19. doi: 10.1186/ar3555
Zorin NA, Arkhipova SV, Zorina VN. Macroglobulin proteins in sepsis. Clinical medicine. 2006; 1: 17-21. Russian (Зорин Н.А., Архипова С.В., Зорина В.Н. Белки семейства макроглобулинов при сепсисе //Клиническая медицина. 2006. № 1. С. 17-21)
Zorina VN, Zorin NA. Protein components of innate immunity in protection from pathogenic invasion (literature review). Journal of microbiology epidemiology immunobiology. 2013; 3: 111-117. Russian (Зорина В.Н., Зорин Н.А. Белковые компоненты врожденного иммунитета в защите от патогенной инвазии //ЖМЭИ. 2013. № 3. С. 111-117)
Wei S, Luo C, YuS, Gao J, Liu C, Wei Z et al. Erythropoietin ameliorates early brain injury after subarachnoid haemorrhage by modulating microglia polarization via the EPOR/JAK2-STAT3 pathway. Exp Cell Res. 2017; 361(2): 342-352. doi: 10.1016/j.yexcr.2017.11.002
Renge LV, Bazhenova LG, Zorina VN, Zorina RM, Chirikova TS. Amniotic fluid immunoregulatory proteins in the mono- and mixed carriage of perinatal infection pathogens. Russian Bulletin of Obstetrician-Gynecologist. 2015; 15(6): 17-23. Russian (Ренге Л.В., Баженова Л.Г., Зорина В.Н., Зорина Р.М., Чирикова Т.С. Иммунорегуляторные белки в околоплодных водах при моно- и микстносительстве возбудителей перинатально значимых инфекций //Российский вестник акушера-гинеколога. 2015. Т. 15, № 6. С. 17-23)
