Anti-C1q
Measurement of anti-C1q autoantibodies in patients with Systemic Lupus Erythematosus (SLE) allows for determination of the risk of the development of active lupus nephritis. The BÜHLMANN anti-C1q autoantibody ELISA can be used as an inexpensive and technically simple way to exclude the risk of renal flair in the months following the test with a sensitivity of 95 %. In the case of active lupus nephritis, consecutive determination of anti-C1q antibodies is a tool to evaluate the efficacy of immunosuppressant treatment.

In SLE, anti-C1q autoantibodies are found in up to 50% of patients. However, more than 95% of the patients with lupus nephritis have such antibodies. Anti-C1q autoantibodies are relevant for the follow-up monitoring of lupus patients. Typically an increase in the titer of anti-C1q autoantibodies can be observed between a few weeks and 6 months before a flare of lupus nephritis occurs. Patients without anti-C1q autoantibodies have a very low risk of developing active lupus nephritis within the following 6 months. In contrast, high titers of anti-C1q autoantibodies are not necessarily predictive of a renal flare. However, patients with high or increasing titers of anti-C1q autoantibodies are at 50% risk to develop an active lupus nephritis, particularly if they have suffered from lupus nephritis in the past. A successful treatment of active lupus nephritis typically decreases the titer of anti-C1q autoantibodies. The titers of anti-C1q autoantibodies can drop below the lower limit of detection and remain undetectable even after reduction or termination of immunosuppression.
Product Information
| Anti-C1q | |
|---|---|
Method |
ELISA |
Time to results |
2.5 h |
Sample Type |
20 µl serum or plasma (1:50) |
Standard Range |
5-400 Units/ml |
Sensitivity |
1 unit/ml |
Order Code |
EK-AC1QA 96 wells |
| CE | |
| DOWNLOADS | |||
|---|---|---|---|
Instruction
|
Clinical Information |
Technical Information |
|
English |
[PDF 0.3MB] | [PDF 0.3MB] | [PDF 0.3MB] |
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