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Beyond Uterine Natural Killer Cell Numbers in Unexplained Recurrent Pregnancy Loss: Combined Analysis of CD45, CD56, CD16, CD57, and CD138
Changes in the number and cytotoxic potential of uterine Natural Killer (uNK) cells have been associated with reduced fertility. To provide a better characterization of immunophenotypes in the endometrium of women with uRPL (unexplained recurrent pregnancy loss), we examined the applicability of a s...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7555015/ https://www.ncbi.nlm.nih.gov/pubmed/32872526 http://dx.doi.org/10.3390/diagnostics10090650 |
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author | Chiokadze, Maia Bär, Christin Pastuschek, Jana Dons’koi, Boris V. Khazhylenko, Kseniia G. Schleußner, Ekkehard Markert, Udo R. Favaro, Rodolfo R. |
author_facet | Chiokadze, Maia Bär, Christin Pastuschek, Jana Dons’koi, Boris V. Khazhylenko, Kseniia G. Schleußner, Ekkehard Markert, Udo R. Favaro, Rodolfo R. |
author_sort | Chiokadze, Maia |
collection | PubMed |
description | Changes in the number and cytotoxic potential of uterine Natural Killer (uNK) cells have been associated with reduced fertility. To provide a better characterization of immunophenotypes in the endometrium of women with uRPL (unexplained recurrent pregnancy loss), we examined the applicability of a set of five immune cell markers. The concentration (cells/mm(2)) of CD45(+) leukocytes, CD56(+) uNK cells, and CD138(+) plasma cells as well as of CD16(+) and CD57(+) cells, which indicate high cytotoxic uNK cells, were assessed by immunohistochemistry in endometrial biopsies from 61 uRPL patients and 10 controls. Control fertile endometria presented 90–300 CD56(+) uNK cells/mm(2). uRPL cases were classified in subgroups of low (uRPL-CD56(low) < 90 cells/mm(2)), normal (uRPL-CD56(normal) 90–300 cells/mm(2)), and high uNK cell counts (uRPL-CD56(high) > 300 cells/mm(2)). Some cases from the uRPL-CD56(low) and uRPL-CD56(normal) subgroups showed elevated proportions of cytotoxic CD16(+) and CD57(+) cells in relation to CD56(+) cells. In the uRPL-CD56(high) subgroup, the CD57/CD56 ratio was reduced in most samples and the CD16/CD56 ratio was unaltered. Analysis of CD138 excluded the influence of chronic endometritis on these observations. Our results reinforce a link between uRPL and a dysfunctional endometrial environment associated with distinct immune cell profiles. |
format | Online Article Text |
id | pubmed-7555015 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-75550152020-10-14 Beyond Uterine Natural Killer Cell Numbers in Unexplained Recurrent Pregnancy Loss: Combined Analysis of CD45, CD56, CD16, CD57, and CD138 Chiokadze, Maia Bär, Christin Pastuschek, Jana Dons’koi, Boris V. Khazhylenko, Kseniia G. Schleußner, Ekkehard Markert, Udo R. Favaro, Rodolfo R. Diagnostics (Basel) Article Changes in the number and cytotoxic potential of uterine Natural Killer (uNK) cells have been associated with reduced fertility. To provide a better characterization of immunophenotypes in the endometrium of women with uRPL (unexplained recurrent pregnancy loss), we examined the applicability of a set of five immune cell markers. The concentration (cells/mm(2)) of CD45(+) leukocytes, CD56(+) uNK cells, and CD138(+) plasma cells as well as of CD16(+) and CD57(+) cells, which indicate high cytotoxic uNK cells, were assessed by immunohistochemistry in endometrial biopsies from 61 uRPL patients and 10 controls. Control fertile endometria presented 90–300 CD56(+) uNK cells/mm(2). uRPL cases were classified in subgroups of low (uRPL-CD56(low) < 90 cells/mm(2)), normal (uRPL-CD56(normal) 90–300 cells/mm(2)), and high uNK cell counts (uRPL-CD56(high) > 300 cells/mm(2)). Some cases from the uRPL-CD56(low) and uRPL-CD56(normal) subgroups showed elevated proportions of cytotoxic CD16(+) and CD57(+) cells in relation to CD56(+) cells. In the uRPL-CD56(high) subgroup, the CD57/CD56 ratio was reduced in most samples and the CD16/CD56 ratio was unaltered. Analysis of CD138 excluded the influence of chronic endometritis on these observations. Our results reinforce a link between uRPL and a dysfunctional endometrial environment associated with distinct immune cell profiles. MDPI 2020-08-29 /pmc/articles/PMC7555015/ /pubmed/32872526 http://dx.doi.org/10.3390/diagnostics10090650 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Chiokadze, Maia Bär, Christin Pastuschek, Jana Dons’koi, Boris V. Khazhylenko, Kseniia G. Schleußner, Ekkehard Markert, Udo R. Favaro, Rodolfo R. Beyond Uterine Natural Killer Cell Numbers in Unexplained Recurrent Pregnancy Loss: Combined Analysis of CD45, CD56, CD16, CD57, and CD138 |
title | Beyond Uterine Natural Killer Cell Numbers in Unexplained Recurrent Pregnancy Loss: Combined Analysis of CD45, CD56, CD16, CD57, and CD138 |
title_full | Beyond Uterine Natural Killer Cell Numbers in Unexplained Recurrent Pregnancy Loss: Combined Analysis of CD45, CD56, CD16, CD57, and CD138 |
title_fullStr | Beyond Uterine Natural Killer Cell Numbers in Unexplained Recurrent Pregnancy Loss: Combined Analysis of CD45, CD56, CD16, CD57, and CD138 |
title_full_unstemmed | Beyond Uterine Natural Killer Cell Numbers in Unexplained Recurrent Pregnancy Loss: Combined Analysis of CD45, CD56, CD16, CD57, and CD138 |
title_short | Beyond Uterine Natural Killer Cell Numbers in Unexplained Recurrent Pregnancy Loss: Combined Analysis of CD45, CD56, CD16, CD57, and CD138 |
title_sort | beyond uterine natural killer cell numbers in unexplained recurrent pregnancy loss: combined analysis of cd45, cd56, cd16, cd57, and cd138 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7555015/ https://www.ncbi.nlm.nih.gov/pubmed/32872526 http://dx.doi.org/10.3390/diagnostics10090650 |
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