Cytokines as Biomarkers in Systemic Lupus Erythematosus: Value for Diagnosis and Drug Therapy
Systemic Lupus Erythematosus (SLE) is a chronic autoimmune disease. The disease is characterized by activation and dysregulation of both the innate and the adaptive immune systems. The autoimmune response targets self-molecules including cell nuclei, double stranded DNA and other intra and extracell...
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oai:doaj.org-article:fbe6cb65d46b41c3a5ddafe8b6f429e72021-11-11T16:48:39ZCytokines as Biomarkers in Systemic Lupus Erythematosus: Value for Diagnosis and Drug Therapy10.3390/ijms2221113271422-00671661-6596https://doaj.org/article/fbe6cb65d46b41c3a5ddafe8b6f429e72021-10-01T00:00:00Zhttps://www.mdpi.com/1422-0067/22/21/11327https://doaj.org/toc/1661-6596https://doaj.org/toc/1422-0067Systemic Lupus Erythematosus (SLE) is a chronic autoimmune disease. The disease is characterized by activation and dysregulation of both the innate and the adaptive immune systems. The autoimmune response targets self-molecules including cell nuclei, double stranded DNA and other intra and extracellular structures. Multiple susceptibility genes within the immune system have been identified, as well as disturbances in different immune pathways. SLE may affect different organs and organ systems, and organ involvement is diverse among individuals. A universal understanding of pathophysiological mechanism of the disease, as well as directed therapies, are still missing. Cytokines are immunomodulating molecules produced by cells of the immune system. Interferons (IFNs) are a broad group of cytokines, primarily produced by the innate immune system. The IFN system has been observed to be dysregulated in SLE, and therefore IFNs have been extensively studied with a hope to understand the disease mechanisms and identify novel targeted therapies. In several autoimmune diseases identification and subsequent blockade of specific cytokines has led to successful therapies, for example tumor necrosis factor-alpha (TNF-α) inhibition in rheumatoid arthritis. Authors of this review have sought corresponding developments in SLE. In the current review, we cover the actual knowledge on IFNs and other studied cytokines as biomarkers and treatment targets in SLE.Helena IdborgVilija OkeMDPI AGarticlelupussystemic lupus erythematosusSLEbiomarkerscytokinesinterferonsBiology (General)QH301-705.5ChemistryQD1-999ENInternational Journal of Molecular Sciences, Vol 22, Iss 11327, p 11327 (2021) |
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lupus systemic lupus erythematosus SLE biomarkers cytokines interferons Biology (General) QH301-705.5 Chemistry QD1-999 |
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lupus systemic lupus erythematosus SLE biomarkers cytokines interferons Biology (General) QH301-705.5 Chemistry QD1-999 Helena Idborg Vilija Oke Cytokines as Biomarkers in Systemic Lupus Erythematosus: Value for Diagnosis and Drug Therapy |
description |
Systemic Lupus Erythematosus (SLE) is a chronic autoimmune disease. The disease is characterized by activation and dysregulation of both the innate and the adaptive immune systems. The autoimmune response targets self-molecules including cell nuclei, double stranded DNA and other intra and extracellular structures. Multiple susceptibility genes within the immune system have been identified, as well as disturbances in different immune pathways. SLE may affect different organs and organ systems, and organ involvement is diverse among individuals. A universal understanding of pathophysiological mechanism of the disease, as well as directed therapies, are still missing. Cytokines are immunomodulating molecules produced by cells of the immune system. Interferons (IFNs) are a broad group of cytokines, primarily produced by the innate immune system. The IFN system has been observed to be dysregulated in SLE, and therefore IFNs have been extensively studied with a hope to understand the disease mechanisms and identify novel targeted therapies. In several autoimmune diseases identification and subsequent blockade of specific cytokines has led to successful therapies, for example tumor necrosis factor-alpha (TNF-α) inhibition in rheumatoid arthritis. Authors of this review have sought corresponding developments in SLE. In the current review, we cover the actual knowledge on IFNs and other studied cytokines as biomarkers and treatment targets in SLE. |
format |
article |
author |
Helena Idborg Vilija Oke |
author_facet |
Helena Idborg Vilija Oke |
author_sort |
Helena Idborg |
title |
Cytokines as Biomarkers in Systemic Lupus Erythematosus: Value for Diagnosis and Drug Therapy |
title_short |
Cytokines as Biomarkers in Systemic Lupus Erythematosus: Value for Diagnosis and Drug Therapy |
title_full |
Cytokines as Biomarkers in Systemic Lupus Erythematosus: Value for Diagnosis and Drug Therapy |
title_fullStr |
Cytokines as Biomarkers in Systemic Lupus Erythematosus: Value for Diagnosis and Drug Therapy |
title_full_unstemmed |
Cytokines as Biomarkers in Systemic Lupus Erythematosus: Value for Diagnosis and Drug Therapy |
title_sort |
cytokines as biomarkers in systemic lupus erythematosus: value for diagnosis and drug therapy |
publisher |
MDPI AG |
publishDate |
2021 |
url |
https://doaj.org/article/fbe6cb65d46b41c3a5ddafe8b6f429e7 |
work_keys_str_mv |
AT helenaidborg cytokinesasbiomarkersinsystemiclupuserythematosusvaluefordiagnosisanddrugtherapy AT vilijaoke cytokinesasbiomarkersinsystemiclupuserythematosusvaluefordiagnosisanddrugtherapy |
_version_ |
1718432276865351680 |