ArticleObstetrics and gynecology international2026
Parental KIR/HLA-C Profiles and Reproductive Failure: A Phenotype-Stratified Retrospective Analysis of Couples With Fertility Disorders.
Article in Obstetrics and gynecology international, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
1 citing paper in PubMed.
- Parental KIR/HLA-C Profiles and Reproductive Failure: A Phenotype-Stratified Retrospective Analysis of Couples With Fertility Disorders.Obstetrics and gynecology international · 2026Article
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Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Interactions between maternal killer-cell immunoglobulin-like receptors (KIR) and fetal human leukocyte antigen-C (HLA-C) play a key role in implantation and placentation, yet their clinical relevance remains controversial, partly due to heterogeneous phenotyping of reproductive failure. We conducted a retrospective observational study of 73 biologically comparable clinically referred couples undergoing reproductive immunology assessment. Couples involving donor gametes, surrogacy, or multiple male partners were excluded. Clinical phenotypes were classified as isolated recurrent implantation failure (RIF-only), isolated recurrent pregnancy loss/adverse pregnancy outcome (RPL/APO-only), combined RIF + RPL/APO, or no reproductive failure. Maternal KIR phenotype (AA vs. Bx) was determined by flow cytometry and genetically confirmed. Maternal and paternal HLA-C genotypes were classified as C1C1, C1C2, or C2C2. Associations were assessed using univariable, age-adjusted, and multivariable logistic regression models. Maternal KIR-AA was present in 53.4% of women and was more frequent in the RIF-only group than in the RPL/APO-only group (56.8% vs. 35.3%). In age-adjusted analysis, KIR-AA was associated with increased odds of RIF (OR 2.35;
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