@article{22171, keywords = {Antigens, Bacterial, Biological Assay, Biomarkers, Buffers, Cytokines, Enzyme-Linked Immunosorbent Assay, Glycolipids, Humans, Immunity, Humoral, Interferon-gamma, Interleukin-10, leprosy, Mycobacterium Infections, Reference Values, Sensitivity and Specificity}, author = {Corstjens P and Dood CJ and Ploeg-van Schip JJ and Wiesmeijer K and Riuttamäki T and Meijgaarden K and Spencer JS and Tanke HJ and Ottenhoff T and Geluk A}, title = {Lateral flow assay for simultaneous detection of cellular- and humoral immune responses.}, abstract = {
OBJECTIVE: The development of a cytokine detection assay suitable for detection of multiple biomarkers for improved diagnosis of mycobacterial diseases.
DESIGN AND METHODS: A lateral flow (LF) assay to detect IL-10 was developed utilizing the up-converting phosphor (UCP) reporter-technology. The assay was evaluated using blood samples of leprosy patients. Multiplex applications were explored targeting: 1) IL-10 and IFN-γ in assay buffer; 2) IL-10 and anti-phenolic glycolipid (PGL-I) antibodies in serum from leprosy patients.
RESULTS: Detection of IL-10 below the targeted level of 100pg/mL in serum was shown. Comparison with ELISA showed a quantitative correlation with R(2) value of 0.92. Multiplexing of cytokines and simultaneous detection of cytokine and antibody was demonstrated.
CONCLUSIONS: The UCP-LF IL-10 assay is a user-friendly, rapid alternative for IL-10 ELISAs, suitable for multiplex detection of different cytokines and can be merged with antibody-detection assays to simultaneously detect cellular- and humoral immunity.
}, year = {2011}, journal = {Clinical biochemistry}, volume = {44}, pages = {1241-6}, month = {2011 Oct}, issn = {1873-2933}, url = {http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3177995/pdf/nihms310566.pdf}, doi = {10.1016/j.clinbiochem.2011.06.983}, language = {eng}, }