How the Soluble Human Leukocyte Antigen-G levels in Amniotic Fluid and Maternal Serum Correlate with the Feto-Placental Growth in Uncomplicated Pregnancies

Introduction: Trophoblast-derived angiogenic factors are considered to play an important role in the pathophysiology of various complications of pregnancy. Human Leukocyte Antigen-G (HLA-G) belongs to the non-classical human major histocompatibility complex (MHC-I) molecule and has membrane-bound an...

Teljes leírás

Elmentve itt :
Bibliográfiai részletek
Szerzők: Vincze Márió Attila
Sikovanyecz János Sebestyén
Földesi Imre
Surányi Andrea
Várbíró Szabolcs
Németh Gábor László
Kozinszky Zoltán
Sikovanyecz János
Dokumentumtípus: Cikk
Megjelent: 2024
Sorozat:BIOENGINEERING 11 No. 5
Tárgyszavak:
doi:10.3390/bioengineering11050509

mtmt:34890581
Online Access:http://publicatio.bibl.u-szeged.hu/35397
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245 1 0 |a How the Soluble Human Leukocyte Antigen-G levels in Amniotic Fluid and Maternal Serum Correlate with the Feto-Placental Growth in Uncomplicated Pregnancies  |h [elektronikus dokumentum] /  |c  Vincze Márió Attila 
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490 0 |a BIOENGINEERING  |v 11 No. 5 
520 3 |a Introduction: Trophoblast-derived angiogenic factors are considered to play an important role in the pathophysiology of various complications of pregnancy. Human Leukocyte Antigen-G (HLA-G) belongs to the non-classical human major histocompatibility complex (MHC-I) molecule and has membrane-bound and soluble forms. HLA-G is primarily expressed by extravillous cytotrophoblasts located in the placenta between the maternal and fetal compartments and plays a pivotal role in providing immune tolerance. The aim of this study was to establish a relationship between concentrations of soluble HLA-G (sHLA-G) in maternal serum and amniotic fluid at 16–22 weeks of gestation and the sonographic measurements of fetal and placental growth. Materials and methods: sHLA-G in serum and amniotic fluid, as well as fetal biometric data and placental volume and perfusion indices, were determined in 41 singleton pregnancies with no complications. The level of sHLA-G (U/mL) was tested with a sandwich enzyme-linked immunosorbent assay (ELISA) kit. Results: The sHLA-G levels were unchanged both in amniotic fluid and serum during mid-pregnancy. The sHLA-G level in serum correlated positively with amniotic sHLA-G level (β = 0.63, p < 0.01). Serum sHLA-G level was significantly correlated with abdominal measurements (β = 0.41, p < 0.05) and estimated fetal weight (β = 0.41, p < 0.05). Conversely, amniotic sHLA-G level and placental perfusion (VI: β = −0.34, p < 0.01 and VFI: β = −0.44, p < 0.01, respectively) were negatively correlated. A low amniotic sHLA-G level was significantly associated with nuchal translucency (r = −0.102, p < 0.05). Conclusions: sHLA-G assayed in amniotic fluid might be a potential indicator of placental function, whereas the sHLA-G level in serum can be a prognostic factor for feto-placental insufficiency. 
650 4 |a Klinikai orvostan 
700 0 1 |a Sikovanyecz János Sebestyén  |e aut 
700 0 1 |a Földesi Imre  |e aut 
700 0 1 |a Surányi Andrea  |e aut 
700 0 1 |a Várbíró Szabolcs  |e aut 
700 0 1 |a Németh Gábor László  |e aut 
700 0 1 |a Kozinszky Zoltán  |e aut 
700 0 1 |a Sikovanyecz János  |e aut 
856 4 0 |u http://publicatio.bibl.u-szeged.hu/35397/1/bioengineering-11-00509.pdf  |z Dokumentum-elérés