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Immune Profiling and Precision Medicine in Systemic Lupus Erythematosus

Systemic lupus erythematosus (SLE) is an autoimmune disorder with a wide range of clinical symptoms. Enormous progress has been made in the immunological and genetic understanding of SLE. However, the biology of disease heterogeneity in SLE has remained largely unexplored. Human immune profiling stu...

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Autores principales: Nagafuchi, Yasuo, Shoda, Hirofumi, Fujio, Keishi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6406577/
https://www.ncbi.nlm.nih.gov/pubmed/30744169
http://dx.doi.org/10.3390/cells8020140
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author Nagafuchi, Yasuo
Shoda, Hirofumi
Fujio, Keishi
author_facet Nagafuchi, Yasuo
Shoda, Hirofumi
Fujio, Keishi
author_sort Nagafuchi, Yasuo
collection PubMed
description Systemic lupus erythematosus (SLE) is an autoimmune disorder with a wide range of clinical symptoms. Enormous progress has been made in the immunological and genetic understanding of SLE. However, the biology of disease heterogeneity in SLE has remained largely unexplored. Human immune profiling studies, helped by recent technological advances especially in single-cell and “omics” analyses, are now shedding light on the cellular and molecular basis of clinical symptoms and disease flares in individual patients. Peripheral blood immunophenotyping analysis with flow cytometry or mass cytometry are identifying responsible cell subsets and markers characteristic of disease heterogeneity. Transcriptome analysis is discovering molecular networks responsible for disease activity, disease subtype and future relapse. In this review, we summarize recent advances in the immune profiling analysis of SLE patients and discuss how they will be used for future precision medicine.
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spelling pubmed-64065772019-03-19 Immune Profiling and Precision Medicine in Systemic Lupus Erythematosus Nagafuchi, Yasuo Shoda, Hirofumi Fujio, Keishi Cells Review Systemic lupus erythematosus (SLE) is an autoimmune disorder with a wide range of clinical symptoms. Enormous progress has been made in the immunological and genetic understanding of SLE. However, the biology of disease heterogeneity in SLE has remained largely unexplored. Human immune profiling studies, helped by recent technological advances especially in single-cell and “omics” analyses, are now shedding light on the cellular and molecular basis of clinical symptoms and disease flares in individual patients. Peripheral blood immunophenotyping analysis with flow cytometry or mass cytometry are identifying responsible cell subsets and markers characteristic of disease heterogeneity. Transcriptome analysis is discovering molecular networks responsible for disease activity, disease subtype and future relapse. In this review, we summarize recent advances in the immune profiling analysis of SLE patients and discuss how they will be used for future precision medicine. MDPI 2019-02-10 /pmc/articles/PMC6406577/ /pubmed/30744169 http://dx.doi.org/10.3390/cells8020140 Text en © 2019 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Nagafuchi, Yasuo
Shoda, Hirofumi
Fujio, Keishi
Immune Profiling and Precision Medicine in Systemic Lupus Erythematosus
title Immune Profiling and Precision Medicine in Systemic Lupus Erythematosus
title_full Immune Profiling and Precision Medicine in Systemic Lupus Erythematosus
title_fullStr Immune Profiling and Precision Medicine in Systemic Lupus Erythematosus
title_full_unstemmed Immune Profiling and Precision Medicine in Systemic Lupus Erythematosus
title_short Immune Profiling and Precision Medicine in Systemic Lupus Erythematosus
title_sort immune profiling and precision medicine in systemic lupus erythematosus
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6406577/
https://www.ncbi.nlm.nih.gov/pubmed/30744169
http://dx.doi.org/10.3390/cells8020140
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