Clinical relevance of HEp-2 indirect immunofluorescent patterns: the International Consensus on ANA patterns (ICAP) perspective
- PMID: 30862649
- PMCID: PMC6585284
- DOI: 10.1136/annrheumdis-2018-214436
Clinical relevance of HEp-2 indirect immunofluorescent patterns: the International Consensus on ANA patterns (ICAP) perspective
Abstract
The indirect immunofluorescence assay (IIFA) on HEp-2 cells is widely used for detection of antinuclear antibodies (ANA). The dichotomous outcome, negative or positive, is integrated in diagnostic and classification criteria for several systemic autoimmune diseases. However, the HEp-2 IIFA test has much more to offer: besides the titre or fluorescence intensity, it also provides fluorescence pattern(s). The latter include the nucleus and the cytoplasm of interphase cells as well as patterns associated with mitotic cells. The International Consensus on ANA Patterns (ICAP) initiative has previously reached consensus on the nomenclature and definitions of HEp-2 IIFA patterns. In the current paper, the ICAP consensus is presented on the clinical relevance of the 29 distinct HEp-2 IIFA patterns. This clinical relevance is primarily defined within the context of the suspected disease and includes recommendations for follow-up testing. The discussion includes how this information may benefit the clinicians in daily practice and how the knowledge can be used to further improve diagnostic and classification criteria.
Keywords: ANA patterns; antinuclear antibodies; clinical interpretation; indirect immunofluorescence.
© Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.
Conflict of interest statement
Competing interests: The ICAP committee is funded by unrestricted educational grants by several in vitro diagnostics companies (for details see www.anapatterns.org/sponsors.php). JD has received lecture fees from Euroimmun and Thermo Fisher. MJF is a consultant to Inova Diagnostics and Werfen International; none of the other authors declare any competing interest.
Comment in
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Response to: 'Antinuclear antibodies: mitotic patterns and their clinical associations' by Betancur and Gómez-Puerta.Ann Rheum Dis. 2020 Jun;79(6):e64. doi: 10.1136/annrheumdis-2019-215439. Epub 2019 Apr 29. Ann Rheum Dis. 2020. PMID: 31036627 No abstract available.
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Antinuclear antibodies mitotic patterns and their clinical associations.Ann Rheum Dis. 2020 Jun;79(6):e63. doi: 10.1136/annrheumdis-2019-215428. Epub 2019 Apr 29. Ann Rheum Dis. 2020. PMID: 31036628 No abstract available.
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Response to: 'The utility of the HEp-2000 antinuclear antibody substrate' by Lee et al.Ann Rheum Dis. 2020 Jun;79(6):e68. doi: 10.1136/annrheumdis-2019-215610. Epub 2019 May 14. Ann Rheum Dis. 2020. PMID: 31088789 No abstract available.
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Utility of the HEp-2000 antinuclear antibody substrate.Ann Rheum Dis. 2020 Jun;79(6):e67. doi: 10.1136/annrheumdis-2019-215519. Epub 2019 May 14. Ann Rheum Dis. 2020. PMID: 31088792 No abstract available.
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Decision-making value of nuclear dense fine speckled pattern in systemic autoimmune rheumatic disease: trick or treat?Ann Rheum Dis. 2020 Aug;79(8):e92. doi: 10.1136/annrheumdis-2019-215587. Epub 2019 May 15. Ann Rheum Dis. 2020. PMID: 31092412 No abstract available.
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Response to 'Decision making value of nuclear dense fine speckled pattern in systemic autoimmune rheumatic disease: trick or treat?' by Deng et al.Ann Rheum Dis. 2020 Aug;79(8):e93. doi: 10.1136/annrheumdis-2019-215640. Epub 2019 May 15. Ann Rheum Dis. 2020. PMID: 31092413 No abstract available.
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Titre-specific positive predictive value of antinuclear antibody patterns.Ann Rheum Dis. 2021 Aug;80(8):e128. doi: 10.1136/annrheumdis-2019-216245. Epub 2019 Oct 10. Ann Rheum Dis. 2021. PMID: 31601627 No abstract available.
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Response to 'Titre-specific positive predictive value of anti-nuclear antibody patterns' by Vulsteke et al.Ann Rheum Dis. 2021 Aug;80(8):e129. doi: 10.1136/annrheumdis-2019-216266. Epub 2019 Oct 10. Ann Rheum Dis. 2021. PMID: 31601628 No abstract available.
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