INFLIXIMAB DRUG LEVEL

Immunology

Tumor Necrosis Factor alpha (TNFɑ) belongs to the proinflammatory cytokines which promote and sustain inflammatory reactions. It is produced by macrophages and T cells and plays a central role in both acute and chronic inflammations. Consequently, chronic inflammatory diseases like Crohn’s disease, ulcerative colitis, rheumatoid arthritis, or psoriasis are increasingly being treated with antibodies against TNFɑ, which target directly the underlying inflammatory process.

During recent years, reports of an association between anti-drug antibodies (ADAs) and adverse effects of treatments both in CD and UC have surfaced. Development of ADAs is usually considered to be associated to immunogenicity of monoclonal antibodies. The clinical efficacy of an anti-TNFɑ therapy usually correlates with the trough level of the therapeutic antibody, or the drug level just before the next application of the anti-TNFɑ antibody. Several factors influence the trough level, among them dosage and frequency of anti-TNFɑ blocker infusion, disease activity, individual pharmacokinetics and immune reaction (formation of anti-drug antibodies, ADA)

The IDKmonitor® infliximab drug level ELISA for the determination of the drug level of infliximab (eg REMICADE®) measures quantitatively free infliximab in serum. In combination with the detection of ADA against infliximab, the IDKmonitor®infliximab drug level ELISA is an opportunity for the treating physician to monitor and optimize treatment early on.

Sample Type:

Whole blood: unknown.

Separated: RT 7 days. Longer @ -20ºC

Turnaround Time:

10 working days

Sample Stability:

Whole blood: unknown.

Separated: RT 7 days. Longer @ -20ºC

Instrument / Procedure:

ELISA

Units:

ug/mL

Reference Range:

A detectable anti-TNF trough level (immediately pre-dose) is associated with a higher rate of clinical and endoscopic

remission.

Precautions:
Accreditation Status:
Not Accredited
Testing Laboratory:
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