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10A - Natural Killer Cell Assay in the Blood Is a Useless Investigation

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from Section II - IVF Add-ons

Published online by Cambridge University Press:  25 November 2021

Roy Homburg
Affiliation:
Homerton University Hospital, London
Adam H. Balen
Affiliation:
Leeds Centre for Reproductive Medicine
Robert F. Casper
Affiliation:
Mount Sinai Hospital, Toronto
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Summary

There are many commercial tests for blood immune cell tests looking at NK cell numbers, cell cytotoxicity or associated cytokine levels. Despite the lack of evidence, patients with recurrent pregnancy loss and implantation failure are often advised to have these tests and are subsequently offered immunotherapies, not backed by trial evidence to treat apparently abnormal results. Blood NK cells are innate immune cells and a first line of host defence against pathogens and tumour cells. Uterine NK cells are phenotypically different to blood NK cells and function when activated to promote normal placentation when pregnancy occurs. Despite a lack of biological plausibility, meta-analyses have been suggestive of altered blood NK cells in subfertility and recurrent pregnancy loss. However they have not shown that blood NK cells have an impact on pregnancy outcome. It is imperative that we offer patients tests and treatment based on robust evidence rather than poor science.

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Chapter
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Publisher: Cambridge University Press
Print publication year: 2021

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References

Ander, SE, Diamond, MS, Coyne, CB. Immune responses at the maternal-fetal interface. Sci Immunol. 2019 Jan 11;4(31):eaat6114.CrossRefGoogle ScholarPubMed
Colucci, F. The role of KIR and HLA interactions in pregnancy complications. Immunogenetics. 2017 Aug;69(8–9):557–65.CrossRefGoogle ScholarPubMed
Vento-Tormo, R, Efremova, M, Botting, RA, et al. Single-cell reconstruction of the early maternal-fetal interface in humans. Nature. 2018;563(7731):347–53.CrossRefGoogle ScholarPubMed
Seshadri, S, Sunkara, SK. Natural killer cells in female infertility and recurrent miscarriage: a systematic review and meta-analysis. Hum Reprod Update. 2014 May–June;20(3):429–38.CrossRefGoogle ScholarPubMed
Tang, AW, Alfirevic, Z, Quenby, S. Natural killer cells and pregnancy outcomes in women with recurrent miscarriage and infertility: a systematic review. Hum Reprod. 2011;26(8):1971–80.CrossRefGoogle ScholarPubMed

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