Ingrid Ordás, Brian G. Feagan, William J. Sandborn 

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Presentation transcript:

Therapeutic Drug Monitoring of Tumor Necrosis Factor Antagonists in Inflammatory Bowel Disease  Ingrid Ordás, Brian G. Feagan, William J. Sandborn  Clinical Gastroenterology and Hepatology  Volume 10, Issue 10, Pages 1079-1087 (October 2012) DOI: 10.1016/j.cgh.2012.06.032 Copyright © 2012 AGA Institute Terms and Conditions

Figure 1 Detection of infliximab antibodies (ATIs) by ELISA. The presence of serum IFX lowers detected ATIs or makes them undetectable, thus a negative test with detectable drug is inconclusive. Because this alters the accuracy of the ATI positive test as well, any sample with detectable drug is deemed inconclusive. Clinical Gastroenterology and Hepatology 2012 10, 1079-1087DOI: (10.1016/j.cgh.2012.06.032) Copyright © 2012 AGA Institute Terms and Conditions

Figure 2 Mobility shift assay principle (Prometheus Laboratories). ATI assay: fluorescent-labeled IFX (IFX-488) with a molecular weight of approximately 150 kilodaltons is incubated with serum containing ATI (molecular weight, ∼150–900 kilodaltons). The ATI/IFX immune complexes have a significantly higher molecular weight than the free IFX and can be separated and quantified by size-exclusion high performance liquid chromatography (SE-HPLC) with fluorescent detection. IFX assay: fluorescent-labeled TNF-α (TNF-488, ∼51 kilodaltons) is bound to IFX in the serum. The resulting immune complex has a much higher molecular weight (∼200 kilodaltons) and can be separated by SE-HPLC and monitored by fluorescent detection. Clinical Gastroenterology and Hepatology 2012 10, 1079-1087DOI: (10.1016/j.cgh.2012.06.032) Copyright © 2012 AGA Institute Terms and Conditions

Figure 3 Clinical outcomes to IFX according to serum drug concentration and ATIs. Clinical Gastroenterology and Hepatology 2012 10, 1079-1087DOI: (10.1016/j.cgh.2012.06.032) Copyright © 2012 AGA Institute Terms and Conditions

Figure 4 Proposed treatment algorithm in the setting of loss of response. (1) [IFX], <3 μg/mL; [ADL], <8 μg/mL; [CZP], <27.5 μg/mL. (2) [IFX], 3–7 μg/mL; [ADL], ≥8 μg/mL; [CZP], ≥27.5 μg/mL. (3) [IFX], >7 μg/mL. Additional information is required about the optimal cut-off values for ADL and CZP. Clinical Gastroenterology and Hepatology 2012 10, 1079-1087DOI: (10.1016/j.cgh.2012.06.032) Copyright © 2012 AGA Institute Terms and Conditions