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Article: Autoantibodies in systemic lupus erythematosus: From immunopathology to therapeutic target

TitleAutoantibodies in systemic lupus erythematosus: From immunopathology to therapeutic target
Authors
KeywordsAutoantibody
Autoimmunity
Inflammation
Pathogenesis
SLE
Issue Date1-Oct-2022
PublisherElsevier
Citation
Journal of Autoimmunity, 2022, v. 132 How to Cite?
Abstract

Systemic lupus erythematosus (SLE) is an autoimmune disease characterized by multiple organ inflammatory damage and wide spectrum of autoantibodies. The autoantibodies, especially anti-dsDNA and anti-Sm autoantibodies are highly specific to SLE, and participate in the immune complex formation and inflammatory damage on multiple end-organs such as kidney, skin, and central nervous system (CNS). However, the underlying mechanisms of autoantibody-induced tissue damage and systemic inflammation are still not fully understood. Single cell analysis of autoreactive B cells and monoclonal antibody screening from patients with active SLE has improved our understanding on the origin of autoreactive B cells and the antigen targets of the pathogenic autoantibodies. B cell depletion therapies have been widely studied in the clinics, but the development of more specific therapies against the pathogenic B cell subset and autoantibodies with improved efficacy and safety still remain a big challenge. A more comprehensive autoantibody profiling combined with functional characterization of autoantibodies in diseases development will shed new insights on the etiology and pathogenesis of SLE and guide a specific treatment to individual SLE patients.


Persistent Identifierhttp://hdl.handle.net/10722/328235
ISSN
2023 Impact Factor: 7.9
2023 SCImago Journal Rankings: 2.558
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorLou, HT-
dc.contributor.authorLing, GS-
dc.contributor.authorCao, XT -
dc.date.accessioned2023-06-28T04:39:53Z-
dc.date.available2023-06-28T04:39:53Z-
dc.date.issued2022-10-01-
dc.identifier.citationJournal of Autoimmunity, 2022, v. 132-
dc.identifier.issn0896-8411-
dc.identifier.urihttp://hdl.handle.net/10722/328235-
dc.description.abstract<p><a href="https://www.sciencedirect.com/topics/immunology-and-microbiology/systemic-lupus-erythematosus" title="Learn more about Systemic lupus erythematosus from ScienceDirect's AI-generated Topic Pages">Systemic lupus erythematosus</a> (SLE) is an autoimmune disease characterized by multiple organ inflammatory damage and wide spectrum of autoantibodies. The autoantibodies, especially anti-dsDNA and anti-Sm autoantibodies are highly specific to SLE, and participate in the <a href="https://www.sciencedirect.com/topics/medicine-and-dentistry/antigen-antibody-complex" title="Learn more about immune complex from ScienceDirect's AI-generated Topic Pages">immune complex</a> formation and inflammatory damage on multiple end-organs such as kidney, skin, and <a href="https://www.sciencedirect.com/topics/medicine-and-dentistry/central-nervous-system" title="Learn more about central nervous system from ScienceDirect's AI-generated Topic Pages">central nervous system</a> (CNS). However, the underlying mechanisms of autoantibody-induced tissue damage and <a href="https://www.sciencedirect.com/topics/immunology-and-microbiology/systemic-inflammation" title="Learn more about systemic inflammation from ScienceDirect's AI-generated Topic Pages">systemic inflammation</a> are still not fully understood. <a href="https://www.sciencedirect.com/topics/immunology-and-microbiology/single-cell-analysis" title="Learn more about Single cell analysis from ScienceDirect's AI-generated Topic Pages">Single cell analysis</a> of autoreactive B cells and <a href="https://www.sciencedirect.com/topics/medicine-and-dentistry/monoclonal-antibody" title="Learn more about monoclonal antibody from ScienceDirect's AI-generated Topic Pages">monoclonal antibody</a> screening from <a href="https://www.sciencedirect.com/topics/medicine-and-dentistry/patient" title="Learn more about patients from ScienceDirect's AI-generated Topic Pages">patients</a> with active SLE has improved our understanding on the origin of autoreactive B cells and the antigen targets of the pathogenic autoantibodies. B cell depletion <a href="https://www.sciencedirect.com/topics/medicine-and-dentistry/therapeutic-procedure" title="Learn more about therapies from ScienceDirect's AI-generated Topic Pages">therapies</a> have been widely studied in the clinics, but the development of more specific <a href="https://www.sciencedirect.com/topics/medicine-and-dentistry/therapeutic-procedure" title="Learn more about therapies from ScienceDirect's AI-generated Topic Pages">therapies</a> against the pathogenic <a href="https://www.sciencedirect.com/topics/medicine-and-dentistry/b-lymphocyte-subpopulation" title="Learn more about B cell subset from ScienceDirect's AI-generated Topic Pages">B cell subset</a> and autoantibodies with improved efficacy and safety still remain a big challenge. A more comprehensive autoantibody profiling combined with functional <a href="https://www.sciencedirect.com/topics/medicine-and-dentistry/characterization-of-autoantibody" title="Learn more about characterization of autoantibodies from ScienceDirect's AI-generated Topic Pages">characterization of autoantibodies</a> in diseases development will shed new insights on the etiology and pathogenesis of SLE and guide a specific treatment to individual SLE <a href="https://www.sciencedirect.com/topics/medicine-and-dentistry/patient" title="Learn more about patients from ScienceDirect's AI-generated Topic Pages">patients</a>.<br></p>-
dc.languageeng-
dc.publisherElsevier-
dc.relation.ispartofJournal of Autoimmunity-
dc.subjectAutoantibody-
dc.subjectAutoimmunity-
dc.subjectInflammation-
dc.subjectPathogenesis-
dc.subjectSLE-
dc.titleAutoantibodies in systemic lupus erythematosus: From immunopathology to therapeutic target-
dc.typeArticle-
dc.identifier.doi10.1016/j.jaut.2022.102861-
dc.identifier.scopuseid_2-s2.0-85134746608-
dc.identifier.hkuros344956-
dc.identifier.volume132-
dc.identifier.isiWOS:000891312300006-
dc.identifier.issnl0896-8411-

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