Volume 1173, Issue 1 p. 166-173

Autoantibody Detection Using Indirect Immunofluorescence on HEp-2 Cells

Ulrich Sack

Ulrich Sack

Institute of Clinical Immunology and Transfusion Medicine, Medical Faculty of the University, Leipzig, Germany

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Karsten Conrad

Karsten Conrad

Institute of Immunology, Medical Faculty of the Technical University, Dresden, Germany

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Elena Csernok

Elena Csernok

Department of Rheumatology, University Lübeck and Rheumaklinik Bad Bramstedt, Bad Bramstedt, Germany

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Ingrid Frank

Ingrid Frank

Laboratory Dr. Tiller, Munich, Germany

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Falk Hiepe

Falk Hiepe

Charité-Universitätsmedizin Berlin, Berlin, Germany

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Thorsten Krieger

Thorsten Krieger

Institute of Immunology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany

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Arno Kromminga

Arno Kromminga

Laboratory Lademannbogen, Hamburg, Germany

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Philipp Von Landenberg

Philipp Von Landenberg

Institute of Clinical Chemistry and Laboratory Medicine, Johannes Gutenberg University, Mainz, Germany

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Gerald Messer

Gerald Messer

Department of Dermatology and Allergology, Ludwig-Maximilians University, Munich, Germany

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Torsten Witte

Torsten Witte

Department of Clinical Immunology, Medical School Hannover, Hannover, Germany

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Rudolf Mierau

Rudolf Mierau

Laboratory at Rheumaklinik Aachen, Germany

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for the German EASI (European Autoimmunity Standardization Initiative)

for the German EASI (European Autoimmunity Standardization Initiative)

Institute of Clinical Immunology and Transfusion Medicine, Medical Faculty of the University, Leipzig, Germany

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First published: 01 September 2009
Citations: 73
Address for correspondence: Prof. Dr. Ulrich Sack, Institute of Clinical Immunology and Transfusion Medicine, Medical Faculty of the University, Johannisallee 30, 04103 Leipzig, Germany. Voice: +0341-9725500; fax: +0341-9739367. [email protected]

Abstract

The detection of autoantibodies is an important element in the diagnosis and monitoring of disease progression in patients with autoimmune diseases. In laboratory diagnostic tests for connective tissue and autoimmune liver diseases, indirect immunofluorescence on HEp-2 cells plays a central role in a multistage diagnostic process. Despite the high quality of diagnostics, findings at different laboratories can differ considerably due to a lack of standardization, as well as subjective factors.

The present paper formulates recommendations for the standardized processing and interpretation of the HEp-2 cell test for the detection of non-organ-specific (especially antinuclear) antibodies. It provides requirements regarding the diagnostic tests used, instructions for laboratory procedure and evaluation, and recommendations for interpretation. For an optimal laboratory diagnostic process, it is useful to have an informative, tentative clinical diagnosis and an experienced laboratory diagnostician. In addition, the following key elements are recommended: initial screening using indirect immunofluorescence on carefully chosen HEp-2 cells beginning with a serum dilution of 1:80 and evaluation under a microscope with powerful illumination; results from a titer of 1:160 upwards being considered positive; internal laboratory quality control; and standardized interpretation. The aim is to improve diagnostic tests and care of patients with autoimmune diseases as a central concern of the European Autoimmunity Standardization Initiative (EASI).