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Cytotoxic activity of peripheral blood mononuclear cells in patients with endometriosis: A cross-sectional study

BACKGROUND: Endometriosis is believed to be associated with dysfunction of the lymphocyte population and cytotoxicity of natural killer (NK) cells, induced by the production of interleukin-2 (IL-2). OBJECTIVE: This study aimed to investigate T lymphocytes and NK cell activity in the peripheral blood...

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Autores principales: Muharam, Raden, Bustami, Arleni, Gusti Mansur, Indra, Zulkifli Jacoeb, Teuku, Giustiniani, Jerome, Schiavon, Valerie, Bensussan, Armand
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Knowledge E 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9596928/
https://www.ncbi.nlm.nih.gov/pubmed/36313261
http://dx.doi.org/10.18502/ijrm.v20i8.11758
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author Muharam, Raden
Bustami, Arleni
Gusti Mansur, Indra
Zulkifli Jacoeb, Teuku
Giustiniani, Jerome
Schiavon, Valerie
Bensussan, Armand
author_facet Muharam, Raden
Bustami, Arleni
Gusti Mansur, Indra
Zulkifli Jacoeb, Teuku
Giustiniani, Jerome
Schiavon, Valerie
Bensussan, Armand
author_sort Muharam, Raden
collection PubMed
description BACKGROUND: Endometriosis is believed to be associated with dysfunction of the lymphocyte population and cytotoxicity of natural killer (NK) cells, induced by the production of interleukin-2 (IL-2). OBJECTIVE: This study aimed to investigate T lymphocytes and NK cell activity in the peripheral blood mononuclear cells (PBMCs) of women with endometriosis. MATERIALS AND METHODS: PBMCs were obtained from the peripheral venous blood samples of 14 women with and without endometriosis (n = 7 for each group). Then, the PBMCs were co-cultured for 4 days and were treated with recombinant IL-2 for cytotoxic activity toward target cells (Daudi and K562 cells). The cytotoxicity activity was determined using the 51 chromium release assay before and after stimulation. Flow cytometry measurement was used to examine the expression of T lymphocytes and NK cells before and after being treated with IL-2. RESULTS: The concentration of CD3+CD28+ (co-stimulatory) was significantly lower in the endometriosis group (65.62 [Formula: see text] 5.38) compared to in its counterpart (50.24 [Formula: see text] 4.22) (p = 0.04) before stimulation. However, no significant differences were observed in any other T lymphocytes and NK cells. It was also found that there was a significant increase of CD3-CD28+ after treatment with IL-2 only in the healthy control but not in women with endometriosis. CONCLUSION: Increased expression of CD160 and decreased CD28 play a role in inhibiting NK cell activation and T cell response in women with endometriosis.
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spelling pubmed-95969282022-10-29 Cytotoxic activity of peripheral blood mononuclear cells in patients with endometriosis: A cross-sectional study Muharam, Raden Bustami, Arleni Gusti Mansur, Indra Zulkifli Jacoeb, Teuku Giustiniani, Jerome Schiavon, Valerie Bensussan, Armand Int J Reprod Biomed Original Article BACKGROUND: Endometriosis is believed to be associated with dysfunction of the lymphocyte population and cytotoxicity of natural killer (NK) cells, induced by the production of interleukin-2 (IL-2). OBJECTIVE: This study aimed to investigate T lymphocytes and NK cell activity in the peripheral blood mononuclear cells (PBMCs) of women with endometriosis. MATERIALS AND METHODS: PBMCs were obtained from the peripheral venous blood samples of 14 women with and without endometriosis (n = 7 for each group). Then, the PBMCs were co-cultured for 4 days and were treated with recombinant IL-2 for cytotoxic activity toward target cells (Daudi and K562 cells). The cytotoxicity activity was determined using the 51 chromium release assay before and after stimulation. Flow cytometry measurement was used to examine the expression of T lymphocytes and NK cells before and after being treated with IL-2. RESULTS: The concentration of CD3+CD28+ (co-stimulatory) was significantly lower in the endometriosis group (65.62 [Formula: see text] 5.38) compared to in its counterpart (50.24 [Formula: see text] 4.22) (p = 0.04) before stimulation. However, no significant differences were observed in any other T lymphocytes and NK cells. It was also found that there was a significant increase of CD3-CD28+ after treatment with IL-2 only in the healthy control but not in women with endometriosis. CONCLUSION: Increased expression of CD160 and decreased CD28 play a role in inhibiting NK cell activation and T cell response in women with endometriosis. Knowledge E 2022-09-06 /pmc/articles/PMC9596928/ /pubmed/36313261 http://dx.doi.org/10.18502/ijrm.v20i8.11758 Text en Copyright © 2022 Muharam et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Muharam, Raden
Bustami, Arleni
Gusti Mansur, Indra
Zulkifli Jacoeb, Teuku
Giustiniani, Jerome
Schiavon, Valerie
Bensussan, Armand
Cytotoxic activity of peripheral blood mononuclear cells in patients with endometriosis: A cross-sectional study
title Cytotoxic activity of peripheral blood mononuclear cells in patients with endometriosis: A cross-sectional study
title_full Cytotoxic activity of peripheral blood mononuclear cells in patients with endometriosis: A cross-sectional study
title_fullStr Cytotoxic activity of peripheral blood mononuclear cells in patients with endometriosis: A cross-sectional study
title_full_unstemmed Cytotoxic activity of peripheral blood mononuclear cells in patients with endometriosis: A cross-sectional study
title_short Cytotoxic activity of peripheral blood mononuclear cells in patients with endometriosis: A cross-sectional study
title_sort cytotoxic activity of peripheral blood mononuclear cells in patients with endometriosis: a cross-sectional study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9596928/
https://www.ncbi.nlm.nih.gov/pubmed/36313261
http://dx.doi.org/10.18502/ijrm.v20i8.11758
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