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Analysis of IL-6 and IL-1β release in cryopreserved pooled human whole blood stimulated with endotoxin

To overcome the lack of availability of fresh human whole blood for pyrogen detection, we explored the feasibility of utilizing cryopreserved pooled human blood to detect the responses of the pro-inflammatory cytokines IL-6 and IL-1β to LPS. Whole blood was obtained from five donors and incubated wi...

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Autores principales: He, Qing, Gao, Hua, Xu, Li-ming, Lu, Yan, Wang, Chong, Rui, Jing, Fan, Hua, Wang, Xiu-ying, Wang, Jun-zhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6830915/
https://www.ncbi.nlm.nih.gov/pubmed/29793382
http://dx.doi.org/10.1177/1753425918777596
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author He, Qing
Gao, Hua
Xu, Li-ming
Lu, Yan
Wang, Chong
Rui, Jing
Fan, Hua
Wang, Xiu-ying
Wang, Jun-zhi
author_facet He, Qing
Gao, Hua
Xu, Li-ming
Lu, Yan
Wang, Chong
Rui, Jing
Fan, Hua
Wang, Xiu-ying
Wang, Jun-zhi
author_sort He, Qing
collection PubMed
description To overcome the lack of availability of fresh human whole blood for pyrogen detection, we explored the feasibility of utilizing cryopreserved pooled human blood to detect the responses of the pro-inflammatory cytokines IL-6 and IL-1β to LPS. Whole blood was obtained from five donors and incubated with LPS. The quantities of pro-inflammatory cytokines were measured using ELISA, and the results were compared among the samples. After the blood was cryopreserved with Dimethyl sulfoxide (DMSO) (10% v/v) and stored for 4 mo at –196℃, the detection limits of the IL-6/IL-1β responses to LPS were 0.2/0.4 endotoxin units (EU)/ml, respectively, and IL-6/IL-1β release increased in response to LPS in a dose-dependent manner. When these experiments were performed in three separate laboratories, the within-laboratory reproducibility of the IL-6/IL-1β responses was 100%/86.7%, 93.3%/100%, and 86.7%/80%, and the inter-laboratory reproducibility was 92.9%/85.7%, 64.3%/63.6%, and 57.1%/66.7%, respectively. The sensitivity (the probability of correctly classifying positive samples) and specificity (the probability of correctly classifying negative samples) of the IL-6/IL-1β tests were 81.7%/82.5% and 100%/100%, respectively. The results of this study suggest that cryopreserved pooled blood is a convenient and viable alternative for evaluating in vitro pyrogenicity. Additionally, maintaining cryopreserved pooled blood promotes safety for the user because it is released only after pretesting for infection parameters and has lower variation than fresh donations from a variety of donors.
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spelling pubmed-68309152019-11-20 Analysis of IL-6 and IL-1β release in cryopreserved pooled human whole blood stimulated with endotoxin He, Qing Gao, Hua Xu, Li-ming Lu, Yan Wang, Chong Rui, Jing Fan, Hua Wang, Xiu-ying Wang, Jun-zhi Innate Immun Original Articles To overcome the lack of availability of fresh human whole blood for pyrogen detection, we explored the feasibility of utilizing cryopreserved pooled human blood to detect the responses of the pro-inflammatory cytokines IL-6 and IL-1β to LPS. Whole blood was obtained from five donors and incubated with LPS. The quantities of pro-inflammatory cytokines were measured using ELISA, and the results were compared among the samples. After the blood was cryopreserved with Dimethyl sulfoxide (DMSO) (10% v/v) and stored for 4 mo at –196℃, the detection limits of the IL-6/IL-1β responses to LPS were 0.2/0.4 endotoxin units (EU)/ml, respectively, and IL-6/IL-1β release increased in response to LPS in a dose-dependent manner. When these experiments were performed in three separate laboratories, the within-laboratory reproducibility of the IL-6/IL-1β responses was 100%/86.7%, 93.3%/100%, and 86.7%/80%, and the inter-laboratory reproducibility was 92.9%/85.7%, 64.3%/63.6%, and 57.1%/66.7%, respectively. The sensitivity (the probability of correctly classifying positive samples) and specificity (the probability of correctly classifying negative samples) of the IL-6/IL-1β tests were 81.7%/82.5% and 100%/100%, respectively. The results of this study suggest that cryopreserved pooled blood is a convenient and viable alternative for evaluating in vitro pyrogenicity. Additionally, maintaining cryopreserved pooled blood promotes safety for the user because it is released only after pretesting for infection parameters and has lower variation than fresh donations from a variety of donors. SAGE Publications 2018-05-25 2018-07 /pmc/articles/PMC6830915/ /pubmed/29793382 http://dx.doi.org/10.1177/1753425918777596 Text en © The Author(s) 2018 http://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Articles
He, Qing
Gao, Hua
Xu, Li-ming
Lu, Yan
Wang, Chong
Rui, Jing
Fan, Hua
Wang, Xiu-ying
Wang, Jun-zhi
Analysis of IL-6 and IL-1β release in cryopreserved pooled human whole blood stimulated with endotoxin
title Analysis of IL-6 and IL-1β release in cryopreserved pooled human whole blood stimulated with endotoxin
title_full Analysis of IL-6 and IL-1β release in cryopreserved pooled human whole blood stimulated with endotoxin
title_fullStr Analysis of IL-6 and IL-1β release in cryopreserved pooled human whole blood stimulated with endotoxin
title_full_unstemmed Analysis of IL-6 and IL-1β release in cryopreserved pooled human whole blood stimulated with endotoxin
title_short Analysis of IL-6 and IL-1β release in cryopreserved pooled human whole blood stimulated with endotoxin
title_sort analysis of il-6 and il-1β release in cryopreserved pooled human whole blood stimulated with endotoxin
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6830915/
https://www.ncbi.nlm.nih.gov/pubmed/29793382
http://dx.doi.org/10.1177/1753425918777596
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