Original Approach for Automated Quantification of Antinuclear Autoantibodies by Indirect Immunofluorescence

Introduction. Indirect immunofluorescence (IIF) is the gold standard method for the detection of antinuclear antibodies (ANA) which are essential markers for the diagnosis of systemic autoimmune rheumatic diseases. For the discrimination of positive and negative samples, we propose here an original...

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Main Authors: Daniel Bertin, Noémie Jourde-Chiche, Pierre Bongrand, Nathalie Bardin
Format: Article
Language:English
Published: Wiley 2013-01-01
Series:Clinical and Developmental Immunology
Online Access:http://dx.doi.org/10.1155/2013/182172
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author Daniel Bertin
Noémie Jourde-Chiche
Pierre Bongrand
Nathalie Bardin
author_facet Daniel Bertin
Noémie Jourde-Chiche
Pierre Bongrand
Nathalie Bardin
author_sort Daniel Bertin
collection DOAJ
description Introduction. Indirect immunofluorescence (IIF) is the gold standard method for the detection of antinuclear antibodies (ANA) which are essential markers for the diagnosis of systemic autoimmune rheumatic diseases. For the discrimination of positive and negative samples, we propose here an original approach named Immunofluorescence for Computed Antinuclear antibody Rational Evaluation (ICARE) based on the calculation of a fluorescence index (FI). Methods. We made comparison between FI and visual evaluations on 237 consecutive samples and on a cohort of 25 patients with SLE. Results. We obtained very good technical performance of FI (95% sensitivity, 98% specificity, and a kappa of 0.92), even in a subgroup of weakly positive samples. A significant correlation between quantification of FI and IIF ANA titers was found (Spearman's ρ=0.80, P<0.0001). Clinical performance of ICARE was validated on a cohort of patients with SLE corroborating the fact that FI could represent an attractive alternative for the evaluation of antibody titer. Conclusion. Our results represent a major step for automated quantification of IIF ANA, opening attractive perspectives such as rapid sample screening and laboratory standardization.
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spelling doaj-art-068b7abc2ddc4eeeab0d12d0293612982025-02-03T01:22:38ZengWileyClinical and Developmental Immunology1740-25221740-25302013-01-01201310.1155/2013/182172182172Original Approach for Automated Quantification of Antinuclear Autoantibodies by Indirect ImmunofluorescenceDaniel Bertin0Noémie Jourde-Chiche1Pierre Bongrand2Nathalie Bardin3Aix-Marseille Université, Laboratoire d’Immunologie, Pôle de Biologie, Hôpital de la Conception, Assistance Publique-Hôpitaux de Marseille, 147 boulevard Baille, 13005 Marseille, FranceAix-Marseille Université, Centre de Néphrologie et Transplantation Rénale, Hôpital de la Conception, Assistance Publique-Hôpitaux de Marseille, 13005 Marseille, FranceAix-Marseille Université, Laboratoire d’Immunologie, Pôle de Biologie, Hôpital de la Conception, Assistance Publique-Hôpitaux de Marseille, 147 boulevard Baille, 13005 Marseille, FranceAix-Marseille Université, Laboratoire d’Immunologie, Pôle de Biologie, Hôpital de la Conception, Assistance Publique-Hôpitaux de Marseille, 147 boulevard Baille, 13005 Marseille, FranceIntroduction. Indirect immunofluorescence (IIF) is the gold standard method for the detection of antinuclear antibodies (ANA) which are essential markers for the diagnosis of systemic autoimmune rheumatic diseases. For the discrimination of positive and negative samples, we propose here an original approach named Immunofluorescence for Computed Antinuclear antibody Rational Evaluation (ICARE) based on the calculation of a fluorescence index (FI). Methods. We made comparison between FI and visual evaluations on 237 consecutive samples and on a cohort of 25 patients with SLE. Results. We obtained very good technical performance of FI (95% sensitivity, 98% specificity, and a kappa of 0.92), even in a subgroup of weakly positive samples. A significant correlation between quantification of FI and IIF ANA titers was found (Spearman's ρ=0.80, P<0.0001). Clinical performance of ICARE was validated on a cohort of patients with SLE corroborating the fact that FI could represent an attractive alternative for the evaluation of antibody titer. Conclusion. Our results represent a major step for automated quantification of IIF ANA, opening attractive perspectives such as rapid sample screening and laboratory standardization.http://dx.doi.org/10.1155/2013/182172
spellingShingle Daniel Bertin
Noémie Jourde-Chiche
Pierre Bongrand
Nathalie Bardin
Original Approach for Automated Quantification of Antinuclear Autoantibodies by Indirect Immunofluorescence
Clinical and Developmental Immunology
title Original Approach for Automated Quantification of Antinuclear Autoantibodies by Indirect Immunofluorescence
title_full Original Approach for Automated Quantification of Antinuclear Autoantibodies by Indirect Immunofluorescence
title_fullStr Original Approach for Automated Quantification of Antinuclear Autoantibodies by Indirect Immunofluorescence
title_full_unstemmed Original Approach for Automated Quantification of Antinuclear Autoantibodies by Indirect Immunofluorescence
title_short Original Approach for Automated Quantification of Antinuclear Autoantibodies by Indirect Immunofluorescence
title_sort original approach for automated quantification of antinuclear autoantibodies by indirect immunofluorescence
url http://dx.doi.org/10.1155/2013/182172
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AT noemiejourdechiche originalapproachforautomatedquantificationofantinuclearautoantibodiesbyindirectimmunofluorescence
AT pierrebongrand originalapproachforautomatedquantificationofantinuclearautoantibodiesbyindirectimmunofluorescence
AT nathaliebardin originalapproachforautomatedquantificationofantinuclearautoantibodiesbyindirectimmunofluorescence