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Clinical and Diagnostic Laboratory Immunology, May 2001, p. 471-474, Vol. 8, No. 3
1071-412X/01/$04.00+0   DOI: 10.1128/CDLI.8.3.471-474.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.

High-Quality, Cost-Effective Strategy for Detection of Autoantibodies to Extractable Nuclear Antigens

Tri G. Phan,1,2,* Watson W. S. Ng,1 Dana Bird,2 Kara Smithers,2 Vicky Wong,2 Kerri Gallagher,2 Andrew Williams,2 and Stephen Adelstein1,2

Department of Clinical Immunology1 and Central Sydney Immunology Laboratory,2 Royal Prince Alfred Hospital, Camperdown, New South Wales 2050, Australia

Received 6 November 2000/Returned for modification 6 December 2000/Accepted 10 January 2001

We evaluated methods for the detection of autoantibodies to extractable nuclear antigens (ENAs) to determine the strategy that yielded the most cost effective and clinically meaningful result. We prospectively compared counterimmunoelectrophoresis (CIEP) with and without serum prediffusion (SPD) and found that SPD significantly improved the quality of precipitation lines. This resulted in a decreased requirement for repeat testing and, consequently, was associated with a significant decrease in reagent costs and specimen turnaround time. We also retrospectively compared reactivity by CIEP, CIEP plus SPD, enzyme-linked immunosorbent assay (ELISA), and line immunoassay (LIA) of 52 serum samples that were previously determined to be positive for ENAs, and we correlated the results with clinical diagnoses. There was significant agreement among CIEP, CIEP plus SPD, ELISA, and LIA for the detection of anti-SS-A, anti-SS-B and anti-RNP. In general, CIEP, CIEP plus SPD, and LIA correlated better with the clinical diagnoses than ELISA, even though ELISA detected anti-ENAs more often than the other methods. CIEP plus SPD is therefore the most cost effective method for the identification of clinically meaningful ENAs. Based on our experience, we now screen for ENAs by CIEP, and positive samples are then typed by CIEP plus SPD. Samples that are difficult to interpret are then further assessed by an alternative method.


* Corresponding author. Mailing address: Department of Clinical Immunology, Royal Prince, Alfred Hospital, Missenden Road, Camperdown NSW 2050, Australia. Phone: 61 2 9515 7469. Fax: 61 2 9515 7762. E-mail: tri{at}immu.rpa.cs.nsw.gov.au.


Clinical and Diagnostic Laboratory Immunology, May 2001, p. 471-474, Vol. 8, No. 3
1071-412X/01/$04.00+0   DOI: 10.1128/CDLI.8.3.471-474.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.



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