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Screening of antinuclear antibodies: comparison between enzyme immunoassay based on nuclear homogenates, purified or recombinant antigens and immunofluorescence assay.

Authors :
Bernardini, Sergio
Infantino, Maria
Bellincampi, Lorenza
Nuccetelli, Mania
Afeltra, Antonella
Iori, Roberta
Biroccio, Antonino
Urbani, Andrea
Federici, Giorgio
Source :
Clinical Chemistry & Laboratory Medicine. Oct2004, Vol. 42 Issue 10, p1155-1160. 6p.
Publication Year :
2004

Abstract

Current clinical practice considers antinuclear anti- body (ANA) testing as a screening test; this has a major impact on laboratory work with a growing volume of analyses that need to be performed rapidly, to maintain good specificity and sensitivity. Ongoing discussions have been raised in order to identify the best technology to use in ANA screening, taking into account both clinical and economical implications. The aim of our study was to compare three different enzyme immunoassays (EIA) with immunofluorescence (IF) assay in order to identify which test is better for use as a screening test. The study was performed on 473 sera and the three different EIA tests were based on nuclear homogenates from HeLa cells, purified antigens from HEp-2 cells and recombinant antigens, respectively. The concordance between EIA- ANA and IF-ANA techniques, determined by the Κ statistic, was acceptable, but not complete, and discrepancies between both EIA-positive/IF-negative samples and IF-positive/EIA-negative were found. Both methods show interesting diagnostic abilities, however, the IF-ANA assay seems to be the first choice test in a well-standardized immunofluorescence laboratory with experienced microscopists, whereas the EIA test might be useful especially in large-scale ANA screening. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14346621
Volume :
42
Issue :
10
Database :
Academic Search Index
Journal :
Clinical Chemistry & Laboratory Medicine
Publication Type :
Academic Journal
Accession number :
14674452
Full Text :
https://doi.org/10.1515/CCLM.2004.235