Development and validation of a multiplex fluorescent microsphere immunoassay assay for detection of porcine cytokines

摘要

class="kwd-title">Method name: Fluorescent microsphere immunoassay (FMIA) class="kwd-title">Keywords: Porcine, Multiplex, Cytokine, FMIA, Brain, Placenta, Synovial tissue, Synovial fluid, Plasma, Validation class="head no_bottom_margin" id="abs0010title">AbstractCytokines are cell signalling proteins that mediate a number of different physiological responses. The accurate measurement of cytokine profiles is important for a variety of diagnostic and prognostic scenarios in relation to animal health and welfare. Simultaneous quantification of cytokine profiles in a single sample is now possible using fluorescent microsphere immunoassays (FMIA). We describe the development and validation of a novel multiplex assay using the Bio-Plex^® 200 system to quantify cytokines in five different porcine tissues (brain, placenta, synovial tissue and fluid, plasma). The cytokine profiles are both tissue, and research hypothesis, -dependent but include Interleukin-1beta (IL-1β), Interleukin-4 (IL-4), Interleukin-6 (IL-6), Interleukin-8 (IL-8), Interleukin-10 (IL-10) and Tumor necrosis factor (TNF-α).This methods paper is reported in two parts: the development of a FMIA for porcine tissues and validation of pre-treatment for optimal cytokine recovery in porcine brain, placenta, synovial tissue and plasma. Validation steps are critical in ensuring an assay is suitable for novel sample types.This technique advances traditional ELISAs by: class="first-line-outdent" id="lis0005">

• FMIA provides insight into the profiles of multiple porcine cytokines in certain situations (e.g. disease, parturition).

• Use of the Bio-Plex^® 200 system to investigate novel sample types, including brain, placenta and synovial tissue.

• Multiplexing utilises a fraction of the sample volume compared with multiple ELISAs.