Combined C5aR1 and CD14 inhibition significantly reduced cytokine release induced by both viable and heat inactivated bacteria in human whole blood

2017 ◽  
Vol 89 ◽  
pp. 169-170
Author(s):  
Dorte Christiansen ◽  
Espen Waage Skjeflo ◽  
Anne Landsem ◽  
Hilde Fure ◽  
Judith K. Ludviksen ◽  
...  
2009 ◽  
Vol 33 (6) ◽  
pp. 583-586 ◽  
Author(s):  
Friederike Traunmüller ◽  
Christiane Thallinger ◽  
Johann Hausdorfer ◽  
Christopher Lambers ◽  
Stanislava Tzaneva ◽  
...  

2002 ◽  
Vol 9 (3) ◽  
pp. 588-597 ◽  
Author(s):  
Yukari Nakagawa ◽  
Hideko Maeda ◽  
Toshimi Murai

ABSTRACT The reliability of an in vitro pyrogen test system based on proinflammatory cytokine release from human monocytic cells was assessed by comparison with a test system based on a human whole blood culture as well as with the conventional rabbit pyrogen test. The human cells used as the pyrogen indicator cells were newly selected by subcloning of a human monocytic cell line, Mono-Mac-6. The selected cells, named MM6-CA8, responded to various pyrogens, including endotoxin, peptidoglycan (PG), Staphylococcus aureus Cowan 1 (SAC), and poly(I ·  C), with a high sensitivity and produced proinflammatory cytokines, such as interleukin 1 (IL-1), IL-6, and tumor necrosis factor alpha. Among these cytokines, IL-6 was produced most sensitively in response to traces of the pyrogens and detected in the largest quantities in the culture medium. The cytokine-producing responses of MM6-CA8 cells correlated significantly with the responses of cultured human whole blood, which represents an ex vivo culture test system reproducing pyrogen-induced cytokine production in the human body. In terms of cytokine inducibility, the pyrogens were ranked in the order endotoxin > PG > poly (I · C) > SAC in both culture systems, a ranking which almost agreed with the ranking of their pyrogenicity as assessed by the rabbit pyrogen test. These results suggest that the in vitro responsiveness of MM6-CA8 cells to various pyrogens is highly relevant for human pyrogenic reactions. Therefore, the in vitro test system is useful and reliable for detecting the presence of materials that are pyrogenic for humans.


2020 ◽  
Vol 107 (4) ◽  
pp. 673-683 ◽  
Author(s):  
Birgitta Ehrnström ◽  
June F. Kojen ◽  
Miriam Giambelluca ◽  
Liv Ryan ◽  
Siv H. Moen ◽  
...  

2017 ◽  
Vol 37 (12) ◽  
pp. 531-540 ◽  
Author(s):  
Merel Van Walleghem ◽  
Kevin Tabury ◽  
Rodrigo Fernandez-Gonzalo ◽  
Ann Janssen ◽  
Judith-Irina Buchheim ◽  
...  

2018 ◽  
Vol 2018 ◽  
pp. 1-9
Author(s):  
H. W. Grievink ◽  
M. Moerland

Human whole blood cultures are widely used for the investigation of physiological pathways and drug effectsin vitro. Detailed information on the effect of “sample aging” (the time span between blood collection and experimental start) on the experimental outcome is not readily available in the public domain. We studied the effect of sample aging on the ability of immune cells to respond to cell-specific immune triggers (LPS, PMA/ionomycin, and SEB). Sample aging at room temperature profoundly inhibited the LPS-induced monocytic cytokine release in minimally diluted whole blood cultures. The reduction ranged from 20–50% after 30 minutes to 80–100% after 10 hours and differed between cytokines (IL-1β, IL-2, IL-6, IFNγ, and TNFα). Sample storage at 4°C or 37°C even worsened this. PMA/ionomycin- and SEB-induced cytokine release, both mainly T-cell-driven, were also reduced by sample aging but to a lesser extent (20–50% after 24 hours). Intracellular cytokine staining revealed that the number of LPS-responding cells was not impacted by sample aging and reduced LPS responsivity could also not be explained by apoptosis or downregulated TLR4 expression. Thus, we speculate that sample aging induces an inhibitory pathway downstream from TLR4 in monocytes. These results underline the importance of quick sample handling when investigating innate immune responses in whole blood, especially for monocyte responses.


2003 ◽  
Vol 188 (6) ◽  
pp. 938-943 ◽  
Author(s):  
Sonja von Aulock ◽  
Nicolas W. J. Schröder ◽  
Katja Gueinzius ◽  
Stephanie Traub ◽  
Sebastian Hoffmann ◽  
...  

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