KIR und HLA

In diesem Ordner sollen Studien zur Reproduktionsmedizin gesammelt werden.
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Sonnenschein007
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KIR und HLA

Beitrag von Sonnenschein007 »

https://www.fertstert.org/article/S0015 ... 5/fulltext



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VIEWS AND REVIEWS| VOLUME 107, ISSUE 6, P1273-1278, JUNE 01, 2017
Why natural killer cells are not enough: a further understanding of killer immunoglobulin-like receptor and human leukocyte antigen
Diana Alecsandru, M.D., Ph.D.
Juan A. García-Velasco, M.D., Ph.D. Published:May 10, 2017DOI:https://doi.org/10.1016/j.fertnstert.2017.04.018
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Abstract
The immune system's role in recurrent reproductive failure is a controversial issue in assisted reproduction. Most studies into immune system implication in reproduction have focused on finding markers of peripheral blood and less on the uterine environment. Peripheral blood natural killer cells have become an "immune study core" for women with recurrent miscarriage or recurrent implantation failure, based on the mistaken notion that they cause reproductive failure by killing or "rejecting" the embryo. Maternal-fetal tolerance begins at the uterine level, so successful adaptation to the fetus occurs after a complicated process. Insufficient uterine lining invasion by an invading extravillous trophoblast is the primary defect in pregnancy disorders such as recurrent miscarriage. This process is regulated by the interaction between maternal killer immunoglobulin-like receptors (KIRs), expressed by uterine natural killer cells (uNK), and their ligand human leukocyte antigen (HLA) C, expressed by the extravillous trophoblast. Pregnancies are an increased risk of disorders in mothers with KIR AA when the fetus has paternal HLA-C2. A recent report has indicated that the expression of more than one paternal HLA-C by the extravillous trophoblast in assisted reproduction may affect placentation in mothers with KIR AA. This review provides insight into the immune system's role in assisted reproductive treatments. These insights can have an impact on the selection of single-embryo transfer and/or oocyte/sperm donor according to HLA-C in patients with recurrent implantation failure and recurrent miscarriage depending on their KIR haplotype.
Sonnenschein007
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Re: KIR und HLA

Beitrag von Sonnenschein007 »

Und hier ein Artikel mit ein paar Zahlen zu lebendgeburtenrate etc und kir:

J Clin Med. 2023 Mar; 12(5): 1905. Published online 2023 Feb 28. doi: 10.3390/jcm12051905
PMCID: PMC10004330PMID: 36902692
The Influence of Maternal KIR Haplotype on the Reproductive Outcomes after Single Embryo Transfer in IVF Cycles in Patients with Recurrent Pregnancy Loss and Implantation Failure—A Single Center Experience


https://www.ncbi.nlm.nih.gov/pmc/articl ... 5%25%20IVF).

Abstract
(1) Background: Recurrent pregnancy loss (RPL) and recurrent implantation failure (RIF) have in common a deficient maternal adaptation to the semi-allogeneic fetus, in which killer immunoglobulin-like receptor (KIR) family expressed by natural killer (NK) cells play an important role. The aim of this study was to evaluate the influence of maternal KIR haplotype on the reproductive outcomes after single embryo transfer in IVF cycles in patients with RPL and RIF. (2) Methods: Patients with RIF and RPL who presented at Origyn Fertility Center from Iasi, Romania, were prospectively enrolled between January 2020 and December 2022. Clinical and paraclinical data was examined. Descriptive statistics and a conditional logistic regression model were used to analyze our data. (3) Results: Patients with a KIR AA haplotype had significantly more chances of miscarriage if they underwent an IVF procedure (aOR: 4.15, 95% CI: 1.39–6.50, p = 0.032) compared with those who spontaneously achieved a pregnancy. Moreover, it appeared that the same haplotype increased the chances of obtaining a pregnancy for patients who underwent an IVF procedure (aOR: 2.57, 95% CI: 0.85–6.75, p = 0.023). (4) Conclusions: Determination of KIR haplotype could be beneficial for patients with RPL or RIF in order to offer an individualized management.

Keywords: recurrent pregnancy loss, recurrent implantation failure, Kir haplotype, HLA-C
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