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Different Background: Natural Killer Cell Profiles in Secondary versus Primary Recurrent Pregnancy Loss
(1) Background: Prior studies suggested a significant impact of previous live births on peripheral natural killer cells (pNK) in patients with recurrent pregnancy loss (RPL). Patients with primary RPL (pRPL, no live birth) showed higher numbers of pNK than secondary RPL patients (sRPL, ≥ 1 live birt...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7826987/ https://www.ncbi.nlm.nih.gov/pubmed/33430491 http://dx.doi.org/10.3390/jcm10020194 |
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author | Strobel, Laura Vomstein, Kilian Kyvelidou, Christiana Hofer-Tollinger, Susanne Feil, Katharina Kuon, Ruben-Jeremias Ebner, Susanne Troppmair, Jakob Toth, Bettina |
author_facet | Strobel, Laura Vomstein, Kilian Kyvelidou, Christiana Hofer-Tollinger, Susanne Feil, Katharina Kuon, Ruben-Jeremias Ebner, Susanne Troppmair, Jakob Toth, Bettina |
author_sort | Strobel, Laura |
collection | PubMed |
description | (1) Background: Prior studies suggested a significant impact of previous live births on peripheral natural killer cells (pNK) in patients with recurrent pregnancy loss (RPL). Patients with primary RPL (pRPL, no live birth) showed higher numbers of pNK than secondary RPL patients (sRPL, ≥ 1 live birth). (2) Methods: To further determine immunological differences between RPL patients and controls, we analysed pNK subpopulations and activation markers in pRPL (n = 47), sRPL (n = 24) and controls with previous live birth (sCtrl, n = 25) and nullipara (pCtrl, n = 60) within a prospective study. Percentages and numbers of CD56(dim)CD16(bright) cells, subpopulations and activation markers (CD57+, CD62L+, NKG2D+, NKp46+) were measured in non-pregnant RPL patients and n = 85 controls (n = 60 pCtrl, n = 25 sCtrl) in the mid-luteal phase by flow cytometry. (3) Results: Compared to sRPL patients, sCtrls showed higher CD56(+) and CD56(dim)CD16(bright) numbers. Further, sRPL patients showed lower numbers of CD56(dim)CD16(bright)NKG2D(+) and CD56(dim)CD16(bright)NKp46(+) than sCtrls. (4) Conclusion: We suggest a chronic immune stimulation leading to a lower NK-cell count in sRPL patients with a lower NK cytotoxicity. This underlines the necessity to investigate pNK subpopulations as well as pRPL and sRPL separately to delineate the immune alterations in RPL. |
format | Online Article Text |
id | pubmed-7826987 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-78269872021-01-25 Different Background: Natural Killer Cell Profiles in Secondary versus Primary Recurrent Pregnancy Loss Strobel, Laura Vomstein, Kilian Kyvelidou, Christiana Hofer-Tollinger, Susanne Feil, Katharina Kuon, Ruben-Jeremias Ebner, Susanne Troppmair, Jakob Toth, Bettina J Clin Med Article (1) Background: Prior studies suggested a significant impact of previous live births on peripheral natural killer cells (pNK) in patients with recurrent pregnancy loss (RPL). Patients with primary RPL (pRPL, no live birth) showed higher numbers of pNK than secondary RPL patients (sRPL, ≥ 1 live birth). (2) Methods: To further determine immunological differences between RPL patients and controls, we analysed pNK subpopulations and activation markers in pRPL (n = 47), sRPL (n = 24) and controls with previous live birth (sCtrl, n = 25) and nullipara (pCtrl, n = 60) within a prospective study. Percentages and numbers of CD56(dim)CD16(bright) cells, subpopulations and activation markers (CD57+, CD62L+, NKG2D+, NKp46+) were measured in non-pregnant RPL patients and n = 85 controls (n = 60 pCtrl, n = 25 sCtrl) in the mid-luteal phase by flow cytometry. (3) Results: Compared to sRPL patients, sCtrls showed higher CD56(+) and CD56(dim)CD16(bright) numbers. Further, sRPL patients showed lower numbers of CD56(dim)CD16(bright)NKG2D(+) and CD56(dim)CD16(bright)NKp46(+) than sCtrls. (4) Conclusion: We suggest a chronic immune stimulation leading to a lower NK-cell count in sRPL patients with a lower NK cytotoxicity. This underlines the necessity to investigate pNK subpopulations as well as pRPL and sRPL separately to delineate the immune alterations in RPL. MDPI 2021-01-07 /pmc/articles/PMC7826987/ /pubmed/33430491 http://dx.doi.org/10.3390/jcm10020194 Text en © 2021 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 Strobel, Laura Vomstein, Kilian Kyvelidou, Christiana Hofer-Tollinger, Susanne Feil, Katharina Kuon, Ruben-Jeremias Ebner, Susanne Troppmair, Jakob Toth, Bettina Different Background: Natural Killer Cell Profiles in Secondary versus Primary Recurrent Pregnancy Loss |
title | Different Background: Natural Killer Cell Profiles in Secondary versus Primary Recurrent Pregnancy Loss |
title_full | Different Background: Natural Killer Cell Profiles in Secondary versus Primary Recurrent Pregnancy Loss |
title_fullStr | Different Background: Natural Killer Cell Profiles in Secondary versus Primary Recurrent Pregnancy Loss |
title_full_unstemmed | Different Background: Natural Killer Cell Profiles in Secondary versus Primary Recurrent Pregnancy Loss |
title_short | Different Background: Natural Killer Cell Profiles in Secondary versus Primary Recurrent Pregnancy Loss |
title_sort | different background: natural killer cell profiles in secondary versus primary recurrent pregnancy loss |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7826987/ https://www.ncbi.nlm.nih.gov/pubmed/33430491 http://dx.doi.org/10.3390/jcm10020194 |
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