Document Detail


HLA-G and pregnancy adverse outcomes.
MedLine Citation:
PMID:  21376476     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
There is growing evidence that pregnancy complications such as preeclampsia, recurrent pregnancy loss (RPL), IUGR, and premature birth could be associated with abnormal immunologic interactions at the fetal-maternal interface. The restricted expression of HLA-G to the subpopulation of trophoblast cells which invade the uterus has generated much interest. The alternative splicing of HLA-G primary transcript, gives origin to seven isoforms, including both membrane-bound forms (HLA-G1, G2, G3, G4) and soluble forms (sHLA-G: sHLA-G5, G6, G7). sHLA-G consists predominantly of sHLA-G1 after its shedding by metalloproteinases, and secreted sHLA-G5 representing the quantitatively dominating and full-length isoforms. HLA-G expression and HLA-G genetic variations in both the mother and the embryo/fetus may be important for pregnancy outcome. It is also intuitively apparent that a gene with putative immunosuppressive and immunotolerant potential might be functional in both the mother and the embryo/fetus/placenta. Reduced or aberrant HLA-G expression seems to be associated with certain complications of pregnancy, among which preeclampsia and possibly the risk of miscarriage, and that this may be further linked to HLA-G polymorphisms. Most of the studies aimed at assessing the role of HLA-G in pregnant diseases have considered only the maternal genotype and ignored the contribution of the fetus. In this regard, the mother, placenta and the fetus form a synthesis. Therefore, studies on placental diseases should address HLA-G expression and genetic variations also to the fetus/placenta.
Authors:
Monia Cecati; Stefano R Giannubilo; Monica Emanuelli; Andrea L Tranquilli; Franca Saccucci
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Publication Detail:
Type:  Journal Article     Date:  2011-03-03
Journal Detail:
Title:  Medical hypotheses     Volume:  76     ISSN:  1532-2777     ISO Abbreviation:  Med. Hypotheses     Publication Date:  2011 Jun 
Date Detail:
Created Date:  2011-05-13     Completed Date:  2011-09-15     Revised Date:  2011-10-04    
Medline Journal Info:
Nlm Unique ID:  7505668     Medline TA:  Med Hypotheses     Country:  United States    
Other Details:
Languages:  eng     Pagination:  782-4     Citation Subset:  IM    
Copyright Information:
Copyright © 2011 Elsevier Ltd. All rights reserved.
Affiliation:
Dipartimento di Biochimica, Biologia e Genetica, Università Politecnica delle Marche, via Ranieri 65, Ancona 60131, Italy. moniacecati@interfree.it
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MeSH Terms
Descriptor/Qualifier:
Female
HLA Antigens / immunology*
Histocompatibility Antigens Class I / immunology*
Humans
Pregnancy
Pregnancy Complications / immunology*
Pregnancy Outcome*
Chemical
Reg. No./Substance:
0/HLA Antigens; 0/HLA-G antigen; 0/Histocompatibility Antigens Class I
Comments/Corrections
Comment In:
Med Hypotheses. 2011 Sep;77(3):463-4   [PMID:  21700398 ]

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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