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Optimising the collection of female genital tract fluid for cytokine analysis in pregnant women

INTRODUCTION: To better understand the immunology of pregnancy, study of female genital tract fluid (FGF) is desirable. However the optimum method of collection of FGF in pregnant women for immunological methods, specifically cytokine measurement, is unknown. METHODS: A prospective study of HIV-unin...

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Autores principales: Short, C.S., Quinlan, R., Bennett, P., Shattock, R.J., Taylor, G.P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5981004/
https://www.ncbi.nlm.nih.gov/pubmed/29625077
http://dx.doi.org/10.1016/j.jim.2018.03.014
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author Short, C.S.
Quinlan, R.
Bennett, P.
Shattock, R.J.
Taylor, G.P.
author_facet Short, C.S.
Quinlan, R.
Bennett, P.
Shattock, R.J.
Taylor, G.P.
author_sort Short, C.S.
collection PubMed
description INTRODUCTION: To better understand the immunology of pregnancy, study of female genital tract fluid (FGF) is desirable. However the optimum method of collection of FGF in pregnant women for immunological methods, specifically cytokine measurement, is unknown. METHODS: A prospective study of HIV-uninfected pregnant women comparing two methods of FGF collection: polyvinyl acetal sponge collection of cervical fluid (CF) and menstrual cup collection of cervicovaginal fluid (CVF). Samples were collected at 3 time points across the second and third trimesters: 14–21, 22–25 and 26–31 weeks. Multiplex chemi-luminescent assays were used to measure: IFN-γ, IL-1β, IL-2, IL-4, IL-6, IL-8, IL-10, IL-12, IL-13 and TNF-α. Optimal methodology for cytokine normalisation (sample weight, volume and total protein) was explored. RESULTS: All cytokines were measurable in both fluid types. IL-1β, IL-8 and IL-6 were detected at the highest concentrations (ranking order CF > CVF > plasma). CVF collection was simpler, provided the largest volume of sample (median 0.5 g) with the potential for undiluted usage, and allowed for self-insertion. CF cytokine concentrations were intrinsically associated with sample weight and protein concentration however CVF cytokines were independent of these. CONCLUSION: Both methods of collection are robust for measurement of FGF cytokines during pregnancy. We recommend CVF collection using a menstrual cup as a viable option in pregnant women for high dimensional biological techniques.
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spelling pubmed-59810042018-07-01 Optimising the collection of female genital tract fluid for cytokine analysis in pregnant women Short, C.S. Quinlan, R. Bennett, P. Shattock, R.J. Taylor, G.P. J Immunol Methods Article INTRODUCTION: To better understand the immunology of pregnancy, study of female genital tract fluid (FGF) is desirable. However the optimum method of collection of FGF in pregnant women for immunological methods, specifically cytokine measurement, is unknown. METHODS: A prospective study of HIV-uninfected pregnant women comparing two methods of FGF collection: polyvinyl acetal sponge collection of cervical fluid (CF) and menstrual cup collection of cervicovaginal fluid (CVF). Samples were collected at 3 time points across the second and third trimesters: 14–21, 22–25 and 26–31 weeks. Multiplex chemi-luminescent assays were used to measure: IFN-γ, IL-1β, IL-2, IL-4, IL-6, IL-8, IL-10, IL-12, IL-13 and TNF-α. Optimal methodology for cytokine normalisation (sample weight, volume and total protein) was explored. RESULTS: All cytokines were measurable in both fluid types. IL-1β, IL-8 and IL-6 were detected at the highest concentrations (ranking order CF > CVF > plasma). CVF collection was simpler, provided the largest volume of sample (median 0.5 g) with the potential for undiluted usage, and allowed for self-insertion. CF cytokine concentrations were intrinsically associated with sample weight and protein concentration however CVF cytokines were independent of these. CONCLUSION: Both methods of collection are robust for measurement of FGF cytokines during pregnancy. We recommend CVF collection using a menstrual cup as a viable option in pregnant women for high dimensional biological techniques. Elsevier 2018-07 /pmc/articles/PMC5981004/ /pubmed/29625077 http://dx.doi.org/10.1016/j.jim.2018.03.014 Text en © 2018 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Short, C.S.
Quinlan, R.
Bennett, P.
Shattock, R.J.
Taylor, G.P.
Optimising the collection of female genital tract fluid for cytokine analysis in pregnant women
title Optimising the collection of female genital tract fluid for cytokine analysis in pregnant women
title_full Optimising the collection of female genital tract fluid for cytokine analysis in pregnant women
title_fullStr Optimising the collection of female genital tract fluid for cytokine analysis in pregnant women
title_full_unstemmed Optimising the collection of female genital tract fluid for cytokine analysis in pregnant women
title_short Optimising the collection of female genital tract fluid for cytokine analysis in pregnant women
title_sort optimising the collection of female genital tract fluid for cytokine analysis in pregnant women
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5981004/
https://www.ncbi.nlm.nih.gov/pubmed/29625077
http://dx.doi.org/10.1016/j.jim.2018.03.014
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