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Seminal plasma and CD4(+) T-cell cytokine profiles in the in vitro fertilization success

BACKGROUND: Abnormal female immune response is one of the potential causes of unexplained infertility (UI). Seminal plasma (SP) is an important regulator of female immune responses during pregnancy. This study investigated a SP effect on the expression of CD4(+) T-cell-related cytokines in a group o...

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Autores principales: Kanannejad, Zahra, Jahromi, Bahia Namavar, Gharesi-Fard, Behrouz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7212999/
https://www.ncbi.nlm.nih.gov/pubmed/32419783
http://dx.doi.org/10.4103/jrms.JRMS_238_19
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author Kanannejad, Zahra
Jahromi, Bahia Namavar
Gharesi-Fard, Behrouz
author_facet Kanannejad, Zahra
Jahromi, Bahia Namavar
Gharesi-Fard, Behrouz
author_sort Kanannejad, Zahra
collection PubMed
description BACKGROUND: Abnormal female immune response is one of the potential causes of unexplained infertility (UI). Seminal plasma (SP) is an important regulator of female immune responses during pregnancy. This study investigated a SP effect on the expression of CD4(+) T-cell-related cytokines in a group of UI woman candidates for in vitro fertilization (IVF) and healthy fertile women. MATERIALS AND METHODS: This was a semi-experimental study that performed on 20 UI couples (ten unsuccessful and ten successful IVF outcomes) and 10 fertile couples as the healthy group. CD4(+) T-cells were separated from peripheral blood mononuclear cells of women by magnetic-activated cell sorting technique and incubated with (stimulated condition) or without (unstimulated condition) SP of their husbands. After incubation, real-time polymerase chain reaction method was used to investigate interleukin (IL)-23, IL-17, IL-4, IL-10, transforming growth factor (TGF)-β, and interferon (IFN)-γ gene expression. Mann–Whitney U-test, Kruskal–Wallis test, and Wilcoxon signed-rank test were used for statistical analysis. RESULTS: Baseline TCD4(+) mRNA levels of IL-23 (P = 0.03) and TGF-β (P = 0.01) were different between healthy and infertile groups. However, IL-17, IL-4, IFN-γ, and IL-10 were expressed similarly regardless of fertility status. Comparing mRNA expression before and after SP exposure, our results have shown that relative expression of IL-23 significantly increased in successful (P = 0.04) and unsuccessful IVF groups (P = 0.01), whereas IL-10 expression increased only in the IVF failure group (P = 0.01). CONCLUSION: SP can make a positive effect on IVF outcome through alteration in CD4 + T-cell-related cytokines expression, especially IL-10 and IL-23.
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spelling pubmed-72129992020-05-15 Seminal plasma and CD4(+) T-cell cytokine profiles in the in vitro fertilization success Kanannejad, Zahra Jahromi, Bahia Namavar Gharesi-Fard, Behrouz J Res Med Sci Original Article BACKGROUND: Abnormal female immune response is one of the potential causes of unexplained infertility (UI). Seminal plasma (SP) is an important regulator of female immune responses during pregnancy. This study investigated a SP effect on the expression of CD4(+) T-cell-related cytokines in a group of UI woman candidates for in vitro fertilization (IVF) and healthy fertile women. MATERIALS AND METHODS: This was a semi-experimental study that performed on 20 UI couples (ten unsuccessful and ten successful IVF outcomes) and 10 fertile couples as the healthy group. CD4(+) T-cells were separated from peripheral blood mononuclear cells of women by magnetic-activated cell sorting technique and incubated with (stimulated condition) or without (unstimulated condition) SP of their husbands. After incubation, real-time polymerase chain reaction method was used to investigate interleukin (IL)-23, IL-17, IL-4, IL-10, transforming growth factor (TGF)-β, and interferon (IFN)-γ gene expression. Mann–Whitney U-test, Kruskal–Wallis test, and Wilcoxon signed-rank test were used for statistical analysis. RESULTS: Baseline TCD4(+) mRNA levels of IL-23 (P = 0.03) and TGF-β (P = 0.01) were different between healthy and infertile groups. However, IL-17, IL-4, IFN-γ, and IL-10 were expressed similarly regardless of fertility status. Comparing mRNA expression before and after SP exposure, our results have shown that relative expression of IL-23 significantly increased in successful (P = 0.04) and unsuccessful IVF groups (P = 0.01), whereas IL-10 expression increased only in the IVF failure group (P = 0.01). CONCLUSION: SP can make a positive effect on IVF outcome through alteration in CD4 + T-cell-related cytokines expression, especially IL-10 and IL-23. Wolters Kluwer - Medknow 2020-03-18 /pmc/articles/PMC7212999/ /pubmed/32419783 http://dx.doi.org/10.4103/jrms.JRMS_238_19 Text en Copyright: © 2020 Journal of Research in Medical Sciences http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Kanannejad, Zahra
Jahromi, Bahia Namavar
Gharesi-Fard, Behrouz
Seminal plasma and CD4(+) T-cell cytokine profiles in the in vitro fertilization success
title Seminal plasma and CD4(+) T-cell cytokine profiles in the in vitro fertilization success
title_full Seminal plasma and CD4(+) T-cell cytokine profiles in the in vitro fertilization success
title_fullStr Seminal plasma and CD4(+) T-cell cytokine profiles in the in vitro fertilization success
title_full_unstemmed Seminal plasma and CD4(+) T-cell cytokine profiles in the in vitro fertilization success
title_short Seminal plasma and CD4(+) T-cell cytokine profiles in the in vitro fertilization success
title_sort seminal plasma and cd4(+) t-cell cytokine profiles in the in vitro fertilization success
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7212999/
https://www.ncbi.nlm.nih.gov/pubmed/32419783
http://dx.doi.org/10.4103/jrms.JRMS_238_19
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