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Analyses of the clinical and immunological characteristics of patients with lupus erythematosus

BACKGROUND: Lupus erythematosus (LE) is a broad-spectrum, heterogeneous disease. At one end of the spectrum is the cutaneous LE (CLE) without systemic involvement, and at the other end is the systemic LE (SLE) with multisystem involvement. Analyses of clinical and immunological indicators and pathol...

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Autores principales: Deng, Min, Wu, Ruifang, Zhou, Xingyu, Su, Yuwen, Li, Yaping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9455139/
https://www.ncbi.nlm.nih.gov/pubmed/36092230
http://dx.doi.org/10.4103/ijd.ijd_942_20
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author Deng, Min
Wu, Ruifang
Zhou, Xingyu
Su, Yuwen
Li, Yaping
author_facet Deng, Min
Wu, Ruifang
Zhou, Xingyu
Su, Yuwen
Li, Yaping
author_sort Deng, Min
collection PubMed
description BACKGROUND: Lupus erythematosus (LE) is a broad-spectrum, heterogeneous disease. At one end of the spectrum is the cutaneous LE (CLE) without systemic involvement, and at the other end is the systemic LE (SLE) with multisystem involvement. Analyses of clinical and immunological indicators and pathological examinations are helpful for early diagnosis, differential diagnosis, and prognosis of LE. AIM AND OBJECTIVES: We described the clinical and laboratory characteristics of patients with LE and assessed the diagnostic value of immunohistochemical detection of C3d, C4d, IgG, IgG4, and CD123 in skin lesions of LE. MATERIALS AND METHODS: Clinical and laboratory data of 62 patients with LE were collected. The expression levels of C3d, C4d, IgG, IgG4, and CD123 in skin lesions of LE were detected by immunohistochemistry (IHC). RESULTS: Clinical manifestations such as hematological involvement, C3, C4, ESR, hematuresis, proteinuria, anti-Sm, anti-ribosomal P-protein, anti-U1-RNP, anti-histone, and anti-nucleosome antibodies are helpful for classificatory diagnosis of LE. The positive rate of C3d and/or C4d along the basement membrane zone in LE skin lesions by IHC was 74.6%, which was higher than that by direct immunofluorescence (47.5%) (P = 0.002). The expression of CD123 protein and the number of CD123+ plasmacytoid dendritic cells (PDCs) in skin lesions of patients with LE were higher than those of dermatomyositis (DM), while the distributed form of CD123 + PDCs in the dermis was different between LE and DM. CONCLUSIONS: The diagnosis of CLE and SLE requires a combination of clinical manifestations, laboratory indicators, and pathological examination. Immunohistochemical detection of C3d, C4d, and CD123 in skin lesions is important for the classificatory diagnosis of LE.
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spelling pubmed-94551392022-09-09 Analyses of the clinical and immunological characteristics of patients with lupus erythematosus Deng, Min Wu, Ruifang Zhou, Xingyu Su, Yuwen Li, Yaping Indian J Dermatol Original Article BACKGROUND: Lupus erythematosus (LE) is a broad-spectrum, heterogeneous disease. At one end of the spectrum is the cutaneous LE (CLE) without systemic involvement, and at the other end is the systemic LE (SLE) with multisystem involvement. Analyses of clinical and immunological indicators and pathological examinations are helpful for early diagnosis, differential diagnosis, and prognosis of LE. AIM AND OBJECTIVES: We described the clinical and laboratory characteristics of patients with LE and assessed the diagnostic value of immunohistochemical detection of C3d, C4d, IgG, IgG4, and CD123 in skin lesions of LE. MATERIALS AND METHODS: Clinical and laboratory data of 62 patients with LE were collected. The expression levels of C3d, C4d, IgG, IgG4, and CD123 in skin lesions of LE were detected by immunohistochemistry (IHC). RESULTS: Clinical manifestations such as hematological involvement, C3, C4, ESR, hematuresis, proteinuria, anti-Sm, anti-ribosomal P-protein, anti-U1-RNP, anti-histone, and anti-nucleosome antibodies are helpful for classificatory diagnosis of LE. The positive rate of C3d and/or C4d along the basement membrane zone in LE skin lesions by IHC was 74.6%, which was higher than that by direct immunofluorescence (47.5%) (P = 0.002). The expression of CD123 protein and the number of CD123+ plasmacytoid dendritic cells (PDCs) in skin lesions of patients with LE were higher than those of dermatomyositis (DM), while the distributed form of CD123 + PDCs in the dermis was different between LE and DM. CONCLUSIONS: The diagnosis of CLE and SLE requires a combination of clinical manifestations, laboratory indicators, and pathological examination. Immunohistochemical detection of C3d, C4d, and CD123 in skin lesions is important for the classificatory diagnosis of LE. Wolters Kluwer - Medknow 2022 /pmc/articles/PMC9455139/ /pubmed/36092230 http://dx.doi.org/10.4103/ijd.ijd_942_20 Text en Copyright: © 2022 Indian Journal of Dermatology https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Deng, Min
Wu, Ruifang
Zhou, Xingyu
Su, Yuwen
Li, Yaping
Analyses of the clinical and immunological characteristics of patients with lupus erythematosus
title Analyses of the clinical and immunological characteristics of patients with lupus erythematosus
title_full Analyses of the clinical and immunological characteristics of patients with lupus erythematosus
title_fullStr Analyses of the clinical and immunological characteristics of patients with lupus erythematosus
title_full_unstemmed Analyses of the clinical and immunological characteristics of patients with lupus erythematosus
title_short Analyses of the clinical and immunological characteristics of patients with lupus erythematosus
title_sort analyses of the clinical and immunological characteristics of patients with lupus erythematosus
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9455139/
https://www.ncbi.nlm.nih.gov/pubmed/36092230
http://dx.doi.org/10.4103/ijd.ijd_942_20
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