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Soluble CD163 ELISA assay for measuring Macrophage and Monocyte Activation
CD163 is a membrane protein and member of the group B Scavenger Receptor Cysteine-Rich super family specifically expressed on peripheral blood monocytes and macrophages. Macrophages play a central role in the host response to infection and tissue damage, and are furthermore important in the pathogenesis of autoimmune diseases and cancer.
CD163 functions as a scavenger receptor for Haptoglobin-hemoglobin complexes, and furthermore CD163 is involved in the regulation of inflammation. A particularly high expression is seen in macrophages of the ‘alternative activation’ phenotype playing a major role in dampening the inflammatory response and in scavenging components of damaged cells. Soluble plasma CD163 arises from the increased shedding of CD163 mediated by the tumor necrosis factor-α (TNF-α) cleaving enzyme.
Measurement of soluble CD163 (sCD163) may be a valuable marker in researching diseases with macrophage and/or monocyte involvement, such as macrophage activation syndromes (e.g. hemophagocytic syndrome), infections, liver disease (NAFLD/NASH), sepsis, auto-immune disease, chronic inflammatory diseases such as rheumatoid arthritis, atherosclerosis, and various cancers. Additionally, CD163 positive macrophages constitute a major cell subpopulation in human term placenta suggesting a role for the placenta functioning as an active immunosuppressive biological barrier between mother and fetus.
Biomarker for macrophage activation and inflammation research
The assay is based on the principle of the sandwich ELISA. A polyclonal antibody recognizing CD163 is immobilized on the surface of a microtiter plate.
After incubation with the sample or recombinant CD163 standard a second biotinylated monoclonal antibody recognizing CD163 is added. Detection of the latter is done by adding streptavidin-HRP. Using TMB (3, 3’, 5, 5’-tetramethylbenzidine) as substrate for the enzyme HRP, the amount of sCD163 protein can be quantified.