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The Past, Present, and Future in Antinuclear Antibodies (ANA)
Autoantibodies are a hallmark of autoimmunity and, specifically, antinuclear antibodies (ANAs) are the most relevant autoantibodies present in systemic autoimmune rheumatic diseases (SARDs). Over the years, different methods from LE cell to HEp-2 indirect immunofluorescence (IIF), solid-phase assays...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8946865/ https://www.ncbi.nlm.nih.gov/pubmed/35328200 http://dx.doi.org/10.3390/diagnostics12030647 |
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author | Irure-Ventura, Juan López-Hoyos, Marcos |
author_facet | Irure-Ventura, Juan López-Hoyos, Marcos |
author_sort | Irure-Ventura, Juan |
collection | PubMed |
description | Autoantibodies are a hallmark of autoimmunity and, specifically, antinuclear antibodies (ANAs) are the most relevant autoantibodies present in systemic autoimmune rheumatic diseases (SARDs). Over the years, different methods from LE cell to HEp-2 indirect immunofluorescence (IIF), solid-phase assays (SPAs), and finally multianalyte technologies have been developed to study ANA-associated SARDs. All of them provide complementary information that is important to provide the most clinically valuable information. The identification of new biomarkers together with multianalyte platforms will help close the so-called “seronegative gap” and to correctly classify and diagnose patients with SARDs. Finally, artificial intelligence and machine learning is an area still to be exploited but in a next future will help to extract patterns within patient data, and exploit these patterns to predict patient outcomes for improved clinical management. |
format | Online Article Text |
id | pubmed-8946865 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-89468652022-03-25 The Past, Present, and Future in Antinuclear Antibodies (ANA) Irure-Ventura, Juan López-Hoyos, Marcos Diagnostics (Basel) Review Autoantibodies are a hallmark of autoimmunity and, specifically, antinuclear antibodies (ANAs) are the most relevant autoantibodies present in systemic autoimmune rheumatic diseases (SARDs). Over the years, different methods from LE cell to HEp-2 indirect immunofluorescence (IIF), solid-phase assays (SPAs), and finally multianalyte technologies have been developed to study ANA-associated SARDs. All of them provide complementary information that is important to provide the most clinically valuable information. The identification of new biomarkers together with multianalyte platforms will help close the so-called “seronegative gap” and to correctly classify and diagnose patients with SARDs. Finally, artificial intelligence and machine learning is an area still to be exploited but in a next future will help to extract patterns within patient data, and exploit these patterns to predict patient outcomes for improved clinical management. MDPI 2022-03-07 /pmc/articles/PMC8946865/ /pubmed/35328200 http://dx.doi.org/10.3390/diagnostics12030647 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Irure-Ventura, Juan López-Hoyos, Marcos The Past, Present, and Future in Antinuclear Antibodies (ANA) |
title | The Past, Present, and Future in Antinuclear Antibodies (ANA) |
title_full | The Past, Present, and Future in Antinuclear Antibodies (ANA) |
title_fullStr | The Past, Present, and Future in Antinuclear Antibodies (ANA) |
title_full_unstemmed | The Past, Present, and Future in Antinuclear Antibodies (ANA) |
title_short | The Past, Present, and Future in Antinuclear Antibodies (ANA) |
title_sort | past, present, and future in antinuclear antibodies (ana) |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8946865/ https://www.ncbi.nlm.nih.gov/pubmed/35328200 http://dx.doi.org/10.3390/diagnostics12030647 |
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