Skip to main content
DNA Labs India

Infliximab Anti-TNF Blocker Test

DNA Labs India | ISO 9001:2015 Certified

Infliximab Anti-TNF Blocker Test

Short Name: Infliximab Drug Level

Also known as: Infliximab Drug Level Test, Infliximab Trough Level Test, Infliximab Quantitation Test, Anti-TNF Drug Monitoring Test

Infliximab Anti-TNF Blocker Test test available at DNA Labs India for ₹32,000. Uses ELISA (Enzyme-Linked Immunosorbent Assay) on Serum samples. Results in Reports are typically available within 2-3 weeks after sample collection. Samples collected by the 7th of the month are processed with results delivered after 2-3 weeks.. Free home collection in 300+ cities across India.

Gastroenterologist, RheumatologistAdults🏠 Home Collection

Overview

The Infliximab Anti-TNF Blocker Test is performed to measure the trough serum concentration of Infliximab in patients receiving anti-TNF therapy. This test helps clinicians evaluate whether a patient has achieved therapeutic drug levels, assess the cause of treatment failure or loss of response, optimize dosing strategies, detect the presence of anti-drug antibodies indirectly through low trough levels, and guide decisions regarding dose escalation, treatment switching, or discontinuation. It is an integral component of personalized medicine in the management of chronic inflammatory diseases.

Test Code
1112
CPT Code
80299
ICD Code
Z51.81
Price
₹32,000
Sample Type
Serum
Result Time
Reports are typically available within 2-3 weeks after sample collection. Samples collected by the 7th of the month are processed with results delivered after 2-3 weeks.
Fasting Required
No
Method
ELISA (Enzyme-Linked Immunosorbent Assay)
Step 1

Sample Collection

The patient should be scheduled for sample collection just before the next scheduled Infliximab dose (trough level). No fasting is required. Inform the laboratory of current medications including immunomodulators, corticosteroids, and the date and dose of the last Infliximab infusion.

Method: Venipuncture

Step 2

Laboratory Analysis

A standard venipuncture will be performed to collect 3 mL of blood into a Serum Separator Tube (SST). The procedure typically takes less than 5 minutes.

Step 3

Report Delivery

Apply gentle pressure to the venipuncture site. The sample will be processed, refrigerated or frozen as required, and dispatched to the laboratory for ELISA-based analysis.

Timeline: Reports are typically available within 2-3 weeks after sample collection. Samples collected by the 7th of the month are processed with results delivered after 2-3 weeks.

Patient Instructions

1
Before the Test:No special preparation or fasting is required. Schedule your sample collection just before your next scheduled Infliximab infusion (trough level). Inform the phlebotomist and laboratory about your current medications, last infusion date and dosage, and any concurrent immunomodulatory therapy.
2
During the Test:A trained phlebotomist will collect approximately 3 mL of blood from a vein in your arm using a standard venipuncture procedure. The blood will be collected into a Serum Separator Tube (SST). The entire process typically takes less than 5 minutes.
3
After the Test:After blood collection, gentle pressure will be applied to the puncture site. You may resume normal activities immediately. The sample will be processed and analyzed using ELISA methodology. Reports will be available within 2-3 weeks via online portal, email, or WhatsApp.

About This Test

Who Should Get This Test

The Infliximab Anti-TNF Blocker Test is performed to measure the trough serum concentration of Infliximab in patients receiving anti-TNF therapy. This test helps clinicians evaluate whether a patient has achieved therapeutic drug levels, assess the cause of treatment failure or loss of response, optimize dosing strategies, detect the presence of anti-drug antibodies indirectly through low trough levels, and guide decisions regarding dose escalation, treatment switching, or discontinuation. It is an integral component of personalized medicine in the management of chronic inflammatory diseases.

How to Prepare

  • Schedule sample collection just before the next Infliximab infusion (trough level)
  • No fasting is required prior to sample collection
  • Provide complete medication history including immunomodulatory agents
  • Note the date and dosage of the most recent Infliximab infusion
  • Sample stability: Room temperature up to 4 hours, Refrigerated up to 7 days, Frozen up to 14 days
  • Ship the sample refrigerated or frozen to maintain sample integrity

Doctor's Notes

"Infliximab trough level monitoring is essential for patients showing loss of response to anti-TNF therapy. Measuring drug trough concentrations helps clinicians distinguish between inadequate drug levels, which may require dose escalation, and immunogenic loss of response due to anti-drug antibodies, which may necessitate switching to an alternative biologic. This test guides personalized treatment decisions and improves long-term clinical outcomes in patients with inflammatory bowel disease, rheumatoid arthritis, and other inflammatory conditions."

Test Parameters & Specifications

Sample TypeSerum
Sample Volume3 mL (2 mL min.)
ContainerSST (Serum Separator Tube)
Collection MethodVenipuncture

Sample Stability

Room TemperatureUp to 4 hours
Refrigerated (2-8°C)Up to 7 days
Frozen (-20°C or below)Up to 14 days
Sample Rejection Criteria:
  • Sample collected at incorrect time point (not at trough)
  • Hemolyzed, lipemic, or grossly contaminated sample
  • Sample collected in incorrect tube type (non-SST)
  • Insufficient sample volume (less than 2 mL)
  • Sample not stored or shipped at recommended temperature
  • Unlabeled or mislabeled sample

Understanding Your Results

The Infliximab trough concentration is interpreted in the clinical context of the patient's disease activity, treatment goals, concurrent medications, and laboratory markers such as C-reactive protein (CRP) and fecal calprotectin. The following general interpretation framework assists clinicians in making treatment decisions:
📊

Low Infliximab trough levels in a patient with active disease suggest inadequate drug exposure. This may be due to accelerated drug clearance, immunogenic loss of response (presence of anti-drug antibodies), or insufficient dosing. Dose escalation, shortening of infusion intervals, or addition of an immunomodulator may be considered.

Clinical action: Consult treating gastroenterologist or rheumatologist for dose adjustment or therapy modification.

Level: Sub-therapeutic Trough Level

📊

Adequate Infliximab trough levels indicate sufficient drug exposure. If the patient has active disease despite therapeutic drug levels, the inflammation may be driven by non-TNF pathways, and alternative therapeutic mechanisms should be explored.

Clinical action: Discuss with treating specialist regarding disease activity assessment and possible alternative biologic therapy.

Level: Therapeutic Trough Level

📊

Unusually high Infliximab trough levels may suggest reduced drug clearance, particularly in patients with high albumin levels, or may be seen after dose adjustments. While not typically harmful, monitoring for infection risk and dose optimization may be warranted.

Clinical action: Review dosing schedule with treating physician. Monitor for signs of infection.

Level: Supra-therapeutic Trough Level

⚠️ When to Consult a Doctor:

Consult your treating gastroenterologist, rheumatologist, or immunologist if your Infliximab trough levels are below the therapeutic range, if you experience worsening symptoms despite regular Infliximab infusions, if you develop new or unusual symptoms such as persistent fever, infections, or skin reactions during anti-TNF therapy, or if your test results require clinical correlation with disease activity markers.

Limitations

  • This test measures total Infliximab drug levels and does not directly quantify anti-drug antibodies (ADA)
  • Trough levels provide a single time-point measurement and may not fully reflect overall drug exposure
  • Results should always be interpreted in conjunction with clinical assessment, C-reactive protein levels, and other relevant markers
  • The therapeutic range may vary depending on the specific disease being treated and treatment goals
  • ELISA-based assays may show variability between different assay platforms and kits

Risks & Considerations

  • Minor bruising or discomfort at the venipuncture site
  • Rare risk of slight dizziness or lightheadedness during blood draw
  • Extremely rare risk of infection at the puncture site

Interfering Factors

  • Timing of sample collection relative to the Infliximab infusion cycle can significantly affect measured levels
  • Concurrent immunomodulatory therapy (e.g., azathioprine, methotrexate) may influence drug clearance and trough levels
  • High levels of anti-drug antibodies (ADA) may interfere with the assay and lead to falsely low Infliximab levels
  • Severe hypoalbuminemia can accelerate Infliximab clearance and alter trough concentrations
  • Patient body mass index and gender may contribute to inter-individual variability in drug levels
  • Sample hemolysis or lipemia may interfere with ELISA accuracy

Compare With Similar Tests

TestInfliximab Anti-TNF Blocker TestC-Reactive Protein (CRP)Anti-Infliximab Antibodies TestFecal Calprotectin
ComparisonInfliximab Anti-TNF Blocker Test

Frequently Asked Questions

What is the Infliximab Anti-TNF Blocker Test?
The Infliximab Anti-TNF Blocker Test is a specialized blood test that measures the trough (minimum) concentration of Infliximab in your bloodstream. Infliximab is a biologic drug that targets TNF-alpha and is used to treat inflammatory conditions such as Crohn's disease, ulcerative colitis, rheumatoid arthritis, psoriasis, and ankylosing spondylitis. This test helps your doctor determine if you are receiving an adequate dose of the medication.
Why do I need the Infliximab Anti-TNF Blocker Test?
Your doctor may recommend this test if you are not responding adequately to Infliximab therapy, if you have lost response after an initial period of improvement, or as part of routine therapeutic drug monitoring. The test helps distinguish between insufficient drug levels (which may require dose adjustment) and immunogenic failure (which may require switching to a different biologic).
What does a low Infliximab trough level mean?
A low Infliximab trough level suggests that there is insufficient drug in your system to adequately control inflammation. This can be caused by accelerated drug clearance, the development of anti-drug antibodies that neutralize Infliximab, or an insufficient dosing regimen. Your doctor may recommend dose escalation, shortening the interval between infusions, or adding an immunomodulator.
What does a high or therapeutic Infliximab trough level mean?
A therapeutic Infliximab trough level indicates that you have adequate drug concentrations in your blood. If you still have active disease despite therapeutic levels, your doctor may consider that the inflammation is not primarily driven by TNF-alpha and may explore alternative treatment strategies.
When should the blood sample be collected for this test?
The ideal sampling time is just before your next scheduled Infliximab infusion, which represents the trough level (the lowest drug concentration in your dosing cycle). This timing provides the most clinically meaningful measurement. Collecting the sample at other times may lead to misleading results.
Do I need to fast before the Infliximab Anti-TNF Blocker Test?
No, fasting is not required for this test. You can eat and drink normally before sample collection. However, you should ensure that the sample is collected just before your next scheduled Infliximab dose (trough level) for accurate results.
What sample type is required for the Infliximab Anti-TNF Blocker Test?
The test requires 3 mL (minimum 2 mL) of blood collected in a Serum Separator Tube (SST) via standard venipuncture. The sample should be shipped refrigerated or frozen to maintain stability and ensure accurate ELISA-based analysis.
What is the cost of the Infliximab Anti-TNF Blocker Test in India?
The cost of the Infliximab Anti-TNF Blocker Test at DNA Labs India is Rs 32000.0. This price includes free home sample collection for online bookings across India. The test is available in all major cities including Mumbai, Delhi, Bangalore, Hyderabad, Chennai, Kolkata, Pune, Ahmedabad, and many more.
How long does it take to get the Infliximab test results?
The turnaround time for the Infliximab Anti-TNF Blocker Test is approximately 2-3 weeks after sample collection. Samples collected by the 7th of the month are processed with reports delivered after 2-3 weeks. You will receive your results via the online portal, email, or WhatsApp.
What is the ELISA method used in this test?
ELISA (Enzyme-Linked Immunosorbent Assay) is a highly sensitive and specific laboratory technique used to detect and quantify proteins such as Infliximab in blood serum. It uses antigen-antibody interactions and enzymatic color reactions to accurately measure the drug concentration, providing reliable results for therapeutic drug monitoring.
Is home sample collection available for the Infliximab Anti-TNF Blocker Test?
Yes, DNA Labs India offers free home sample collection for the Infliximab Anti-TNF Blocker Test when booked online. This service is available across numerous cities in India, including Mumbai, Delhi, Bangalore, Hyderabad, Ahmedabad, Chennai, Kolkata, Pune, Jaipur, Lucknow, and many more. A trained phlebotomist will visit your home at the scheduled time to collect the sample.
What conditions are treated with Infliximab that may require this monitoring test?
Infliximab is an FDA-approved biologic therapy for several chronic inflammatory conditions including Crohn's Disease, Ulcerative Colitis, Psoriasis, Ankylosing Spondylitis, and Rheumatoid Arthritis. Patients receiving Infliximab for any of these conditions may benefit from trough level monitoring, particularly when there is a loss of response or suboptimal treatment outcomes.
Worried about the process? Our certified phlebotomists collect thousands of samples every month across India. The process takes under 5 minutes and is virtually painless. Questions? Message us on WhatsApp — we're here 7 days a week.

Related Tests

For Hospitals & Clinics

Reference Laboratory Services

We serve as a reference laboratory for hospitals and clinics across India. Send samples from your facility with same-day pickup, priority processing, and results delivered through our online portal. Competitive institutional pricing available.

LIMS Integration

Your Data Privacy

Your medical data is protected under Indian law.

Stored in India: All patient records are stored on servers located in India. No data is transferred outside the country.

DPDP Act Compliant: Under the Digital Personal Data Protection Act 2023, you can request deletion of your records at any time by contacting support.

Book Your Test

Enter your details and we'll connect you within 15 minutes.

🧬

Quick Connect

Enter your mobile number and we’ll connect you with the team.

+91

✅ Connecting you now...

🔒 Your number is used to respond to this request.