Buehlmann


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.

test

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

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BÜHLMANN Laboratories AG
Baselstr. 55
CH-4124 Schönenbuch
Switzerland
Fon: +41 61 487 12 12
Fax: +41 61 487 12 34
info@buhlmannlabs.ch

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