The role of <i>HLA-G</i> gene polymorphism in the formation of pathology in maternal-fetal interface

The relation between polymorphic variants of the HLA-G gene and various pregnancy complications (failure after in vitro fertilization, preeclampsia, spontaneous abortions) is discussed. However, research results vary among women in different populations. It remains unknown whether maternal HLA-G all...

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Main Authors: L. A. Gordeeva, E. N. Voronina, E. G. Polenok, S. A. Mun, R. V. Olennikova, Yu. V. Gareeva, A. N. Glushkov
Format: Article
Language:Russian
Published: St. Petersburg branch of the Russian Association of Allergologists and Clinical Immunologists 2025-03-01
Series:Медицинская иммунология
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Online Access:https://www.mimmun.ru/mimmun/article/view/3203
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author L. A. Gordeeva
E. N. Voronina
E. G. Polenok
S. A. Mun
R. V. Olennikova
Yu. V. Gareeva
A. N. Glushkov
author_facet L. A. Gordeeva
E. N. Voronina
E. G. Polenok
S. A. Mun
R. V. Olennikova
Yu. V. Gareeva
A. N. Glushkov
author_sort L. A. Gordeeva
collection DOAJ
description The relation between polymorphic variants of the HLA-G gene and various pregnancy complications (failure after in vitro fertilization, preeclampsia, spontaneous abortions) is discussed. However, research results vary among women in different populations. It remains unknown whether maternal HLA-G alleles can control congenital malformations (CMs) in the fetus. We studied the role of HLA-G gene polymorphism in the formation of pathology in in maternal-fetal interface using the example of recurrent miscarriage (RM) and CMs in the fetus. We studied 461 women with reproductive pathology and 407 healthy and fertile women having 1-2 children and with no history of pathological pregnancy (control group). The RM group included 151 women with miscarriages before 20 weeks of pregnancy (min = 2; max = 6). The CM group consisted of 310 women with congenital malformations of the fetus. The diagnosis of CM type was carried out according to the International Classification of Diseases, Injuries and Conditions Affecting the Health, Tenth Revision (Q00-Q99). All women provided written informed consent to participate in the study. The rs41551813, rs12722477 and rs41557518 loci of the HLA-G gene were typed by asymmetric real-time PCR. HLA-G 14 bp Ins/Del polymorphism (rs66554220) was determined using electrophoretic separation of amplification products. Polymorphic loci rs41557518 and rs66554220 of HLA-G were linked disequilibrium (D’ = 0.808 (r = 0.017), χ2 = 14.67, d(f) = 3, p = 0.002). Found only highly significant the association of the 110Ile HLA-G allele with the risk of RM in women after statistical correction (OR = 3.03 (1.97-4.64), pcor &lt; 0.0006). Found no statistically significant associations of polymorphic loci rs41551813, rs41557518 and rs66554220 of the HLA-G gene with RM in women. Found no associations of maternal HLA-G polymorphic loci with the risk of CMs in the fetus. It seems the role of individual the HLA-G polymorphic loci in the formation of CMs in the fetus may be minimal. The association of the 110Ile allele (HLA-G*01:04) with RM in women is likely due to its recessive effects on local inflammation.
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spelling doaj-art-582b6a7236014e3c83c44607c20f9e952025-08-04T14:30:44ZrusSt. Petersburg branch of the Russian Association of Allergologists and Clinical ImmunologistsМедицинская иммунология1563-06252313-741X2025-03-0127242342810.15789/1563-0625-TRO-168872001The role of <i>HLA-G</i> gene polymorphism in the formation of pathology in maternal-fetal interfaceL. A. Gordeeva0E. N. Voronina1E. G. Polenok2S. A. Mun3R. V. Olennikova4Yu. V. Gareeva5A. N. Glushkov6Federal Research Center of Coal and Coal Chemistry, Siberian Branch, Russian Academy of Sciences (Institute of Human Ecology, SB RAS)Institute of Chemical Biology and Fundamental Medicine, Siberian Branch, Russian Academy of SciencesFederal Research Center of Coal and Coal Chemistry, Siberian Branch, Russian Academy of Sciences (Institute of Human Ecology, SB RAS)Federal Research Center of Coal and Coal Chemistry, Siberian Branch, Russian Academy of Sciences (Institute of Human Ecology, SB RAS)Kemerovo Regional Clinical HospitalLLC “Medical Practice”Federal Research Center of Coal and Coal Chemistry, Siberian Branch, Russian Academy of Sciences (Institute of Human Ecology, SB RAS)The relation between polymorphic variants of the HLA-G gene and various pregnancy complications (failure after in vitro fertilization, preeclampsia, spontaneous abortions) is discussed. However, research results vary among women in different populations. It remains unknown whether maternal HLA-G alleles can control congenital malformations (CMs) in the fetus. We studied the role of HLA-G gene polymorphism in the formation of pathology in in maternal-fetal interface using the example of recurrent miscarriage (RM) and CMs in the fetus. We studied 461 women with reproductive pathology and 407 healthy and fertile women having 1-2 children and with no history of pathological pregnancy (control group). The RM group included 151 women with miscarriages before 20 weeks of pregnancy (min = 2; max = 6). The CM group consisted of 310 women with congenital malformations of the fetus. The diagnosis of CM type was carried out according to the International Classification of Diseases, Injuries and Conditions Affecting the Health, Tenth Revision (Q00-Q99). All women provided written informed consent to participate in the study. The rs41551813, rs12722477 and rs41557518 loci of the HLA-G gene were typed by asymmetric real-time PCR. HLA-G 14 bp Ins/Del polymorphism (rs66554220) was determined using electrophoretic separation of amplification products. Polymorphic loci rs41557518 and rs66554220 of HLA-G were linked disequilibrium (D’ = 0.808 (r = 0.017), χ2 = 14.67, d(f) = 3, p = 0.002). Found only highly significant the association of the 110Ile HLA-G allele with the risk of RM in women after statistical correction (OR = 3.03 (1.97-4.64), pcor &lt; 0.0006). Found no statistically significant associations of polymorphic loci rs41551813, rs41557518 and rs66554220 of the HLA-G gene with RM in women. Found no associations of maternal HLA-G polymorphic loci with the risk of CMs in the fetus. It seems the role of individual the HLA-G polymorphic loci in the formation of CMs in the fetus may be minimal. The association of the 110Ile allele (HLA-G*01:04) with RM in women is likely due to its recessive effects on local inflammation.https://www.mimmun.ru/mimmun/article/view/3203hla-g genepolymorphismmaternal-fetal interfacepathologyrecurrent miscarriagecongenital malformations
spellingShingle L. A. Gordeeva
E. N. Voronina
E. G. Polenok
S. A. Mun
R. V. Olennikova
Yu. V. Gareeva
A. N. Glushkov
The role of <i>HLA-G</i> gene polymorphism in the formation of pathology in maternal-fetal interface
Медицинская иммунология
hla-g gene
polymorphism
maternal-fetal interface
pathology
recurrent miscarriage
congenital malformations
title The role of <i>HLA-G</i> gene polymorphism in the formation of pathology in maternal-fetal interface
title_full The role of <i>HLA-G</i> gene polymorphism in the formation of pathology in maternal-fetal interface
title_fullStr The role of <i>HLA-G</i> gene polymorphism in the formation of pathology in maternal-fetal interface
title_full_unstemmed The role of <i>HLA-G</i> gene polymorphism in the formation of pathology in maternal-fetal interface
title_short The role of <i>HLA-G</i> gene polymorphism in the formation of pathology in maternal-fetal interface
title_sort role of i hla g i gene polymorphism in the formation of pathology in maternal fetal interface
topic hla-g gene
polymorphism
maternal-fetal interface
pathology
recurrent miscarriage
congenital malformations
url https://www.mimmun.ru/mimmun/article/view/3203
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