T Helper 2-Associated Immunity in the Pathogenesis of Systemic Lupus Erythematosus

Systemic Lupus Erythematosus (SLE) is a chronic autoimmune disease that mainly affects women in their reproductive years. A complex interaction of environmental and genetic factors leads to the disruption of immune tolerance towards self, causing overt immune activation and production of autoantibod...

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Main Authors: Haeun Ko, Chan Johng Kim, Sin-Hyeog Im
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-04-01
Series:Frontiers in Immunology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fimmu.2022.866549/full
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author Haeun Ko
Chan Johng Kim
Chan Johng Kim
Sin-Hyeog Im
Sin-Hyeog Im
Sin-Hyeog Im
author_facet Haeun Ko
Chan Johng Kim
Chan Johng Kim
Sin-Hyeog Im
Sin-Hyeog Im
Sin-Hyeog Im
author_sort Haeun Ko
collection DOAJ
description Systemic Lupus Erythematosus (SLE) is a chronic autoimmune disease that mainly affects women in their reproductive years. A complex interaction of environmental and genetic factors leads to the disruption of immune tolerance towards self, causing overt immune activation and production of autoantibodies that attack multiple organs. Kidney damage, termed lupus nephritis, is the leading cause of SLE-related morbidity and mortality. Autoantibodies are central to propagating lupus nephritis through forming immune complexes and triggering complements. Immunoglobulin G (IgG) potently activates complement; therefore, autoantibodies were mainly considered to be of the IgG isotype. However, studies revealed that over 50% of patients produce autoantibodies of the IgE isotype. IgE autoantibodies actively participate in disease pathogenesis as omalizumab treatment, a humanized anti-IgE monoclonal antibody, improved disease severity in an SLE clinical trial. IgE is a hallmark of T helper 2-associated immunity. Thus, T helper 2-associated immunity seems to play a pathogenic role in a subset of SLE patients. This review summarizes human and animal studies that illustrate type 2 immune responses involved during the pathology of SLE.
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spelling doaj.art-865750bd37c94584b4eaf89bba05d2222022-12-21T23:33:32ZengFrontiers Media S.A.Frontiers in Immunology1664-32242022-04-011310.3389/fimmu.2022.866549866549T Helper 2-Associated Immunity in the Pathogenesis of Systemic Lupus ErythematosusHaeun Ko0Chan Johng Kim1Chan Johng Kim2Sin-Hyeog Im3Sin-Hyeog Im4Sin-Hyeog Im5Department of Life Sciences, Pohang University of Science and Technology, Pohang, South KoreaDepartment of Life Sciences, Pohang University of Science and Technology, Pohang, South KoreaPohang University of Science and Technology (POSTECH) Biotech Center, Pohang University of Science and Technology, Pohang, South KoreaDepartment of Life Sciences, Pohang University of Science and Technology, Pohang, South KoreaInstitute for Convergence Research and Education, Yonsei University, Seoul, South KoreaImmunoBiome Inc., Bio Open Innovation Center, Pohang, South KoreaSystemic Lupus Erythematosus (SLE) is a chronic autoimmune disease that mainly affects women in their reproductive years. A complex interaction of environmental and genetic factors leads to the disruption of immune tolerance towards self, causing overt immune activation and production of autoantibodies that attack multiple organs. Kidney damage, termed lupus nephritis, is the leading cause of SLE-related morbidity and mortality. Autoantibodies are central to propagating lupus nephritis through forming immune complexes and triggering complements. Immunoglobulin G (IgG) potently activates complement; therefore, autoantibodies were mainly considered to be of the IgG isotype. However, studies revealed that over 50% of patients produce autoantibodies of the IgE isotype. IgE autoantibodies actively participate in disease pathogenesis as omalizumab treatment, a humanized anti-IgE monoclonal antibody, improved disease severity in an SLE clinical trial. IgE is a hallmark of T helper 2-associated immunity. Thus, T helper 2-associated immunity seems to play a pathogenic role in a subset of SLE patients. This review summarizes human and animal studies that illustrate type 2 immune responses involved during the pathology of SLE.https://www.frontiersin.org/articles/10.3389/fimmu.2022.866549/fullautoimmunitySLElupus nephritisTh2IL-4IgE
spellingShingle Haeun Ko
Chan Johng Kim
Chan Johng Kim
Sin-Hyeog Im
Sin-Hyeog Im
Sin-Hyeog Im
T Helper 2-Associated Immunity in the Pathogenesis of Systemic Lupus Erythematosus
Frontiers in Immunology
autoimmunity
SLE
lupus nephritis
Th2
IL-4
IgE
title T Helper 2-Associated Immunity in the Pathogenesis of Systemic Lupus Erythematosus
title_full T Helper 2-Associated Immunity in the Pathogenesis of Systemic Lupus Erythematosus
title_fullStr T Helper 2-Associated Immunity in the Pathogenesis of Systemic Lupus Erythematosus
title_full_unstemmed T Helper 2-Associated Immunity in the Pathogenesis of Systemic Lupus Erythematosus
title_short T Helper 2-Associated Immunity in the Pathogenesis of Systemic Lupus Erythematosus
title_sort t helper 2 associated immunity in the pathogenesis of systemic lupus erythematosus
topic autoimmunity
SLE
lupus nephritis
Th2
IL-4
IgE
url https://www.frontiersin.org/articles/10.3389/fimmu.2022.866549/full
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