Development and validation of ELISAs for the quantitation of interleukin (IL)-1β, IL-6, IL-8 and IL-10 in ovine plasma

被引:27
作者
Bouquet, Mahe [1 ,2 ]
Passmore, Margaret R. [1 ,2 ]
Hoe, Louise E. See [1 ,2 ]
Tung, John-Paul [1 ,2 ,3 ]
Simonova, Gabriela [2 ,3 ]
Boon, Ai-Ching [1 ,2 ]
Fraser, John F. [1 ,2 ]
机构
[1] Prince Charles Hosp, Crit Care Res Grp, Brisbane, Qld, Australia
[2] Univ Queensland, Fac Med, Brisbane, Qld, Australia
[3] Australian Red Cross Lifeblood, Res & Dev, Brisbane, Qld, Australia
基金
英国医学研究理事会;
关键词
Cytokines; Inflammation; ELISA; Sheep; MONOCLONAL-ANTIBODIES; ENZYME-IMMUNOASSAY; CONSEQUENCES; CYTOKINES; MODELS;
D O I
10.1016/j.jim.2020.112835
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
There is growing evidence that inflammation underpins many common diseases. Inflammatory/immunomodulatory/immune mediators, such as cytokines, are key modulators of inflammation and mediate both immune cell recruitment and complex intracellular signalling pathways. Ovine models of disease are increasingly utilized in pre-clinical research, however existing methods for measuring cytokine levels are limited. We established and validated enzyme-linked immunosorbent assays (ELISAs) targeting interleukin (IL)-1 beta, IL-6, IL-8 and IL-10 in sheep plasma. These ELISAs showed high sensitivity and specificity with intra- and inter-assay CVs below 10%, and recovery rates between 82 and 123%. Sensitivity for IL-1 beta, IL-6, IL-8 and IL-10 were 117.6 pg/mL, 443.1 pg/mL, 30.9 pg/mL, and 64.3 pg/mL, respectively. ELISA test result reproducibility decreased significantly after 12 weeks of plasma storage at -80 degrees C. Therefore, for accurate cytokine measurements, plasma samples need to be tested within three months of sample collection to account for cytokine protein degradation. These ELISAs offer a reliable and convenient method to identify inflammatory cytokine changes in sheep, allowing key insights into the disease pathogenesis of these ruminants.
引用
收藏
页数:7
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