Glomerular galactose-deficient IgA1 expression analysis in pediatric patients with glomerular diseases

Abstract Galactose-deficient IgA1 (Gd-IgA1) is important in the pathogenesis of IgA nephropathy (IgAN). A Gd-IgA1-specific monoclonal antibody (KM55) has revealed glomerular Gd-IgA1 deposition solely in patients with IgAN and IgA vasculitis with nephritis (IgAV-N). However, this specificity is contr...

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Autores principales: Shinya Ishiko, Tomoko Horinouchi, Rika Fujimaru, Yuko Shima, Hiroshi Kaito, Ryojiro Tanaka, Shingo Ishimori, Atsushi Kondo, Sadayuki Nagai, Yuya Aoto, Nana Sakakibara, China Nagano, Tomohiko Yamamura, Momoka Yoshimura, Koichi Nakanishi, Junya Fujimura, Naohiro Kamiyoshi, Hiroaki Nagase, Norishige Yoshikawa, Kazumoto Iijima, Kandai Nozu
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Publicado: Nature Portfolio 2020
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spelling oai:doaj.org-article:51582829b5bb434c960fdaccff19cb9f2021-12-02T16:46:33ZGlomerular galactose-deficient IgA1 expression analysis in pediatric patients with glomerular diseases10.1038/s41598-020-71101-y2045-2322https://doaj.org/article/51582829b5bb434c960fdaccff19cb9f2020-08-01T00:00:00Zhttps://doi.org/10.1038/s41598-020-71101-yhttps://doaj.org/toc/2045-2322Abstract Galactose-deficient IgA1 (Gd-IgA1) is important in the pathogenesis of IgA nephropathy (IgAN). A Gd-IgA1-specific monoclonal antibody (KM55) has revealed glomerular Gd-IgA1 deposition solely in patients with IgAN and IgA vasculitis with nephritis (IgAV-N). However, this specificity is controversial and has not been demonstrated in pediatric patients. Here, we conducted double-immunofluorescence staining of IgA and Gd-IgA1 in 60 pediatric patients with various glomerular diseases. We divided patients into four groups: (1) patients with IgAN and IgAV-N (n = 23); (2) patients with immunocomplex-mediated glomerulonephritis accompanied by IgA deposition, including lupus nephritis, membranoproliferative glomerulonephritis, and membranous nephropathy (n = 14); (3) patients with other glomerular diseases involving IgA deposition, including idiopathic nephrotic syndrome (INS), oligomeganephronia, Alport syndrome, dense deposit disease, and crescentic glomerulonephritis (n = 11); and (4) patients with IgA-negative diseases including INS, membranoproliferative glomerulonephritis, membranous nephropathy, oligomeganephronia, Alport syndrome, C3 glomerulonephritis, poststreptococcal acute glomerulonephritis, and hemolytic uremic syndrome (n = 12). KM55 staining revealed Gd-IgA1-positive findings in 23/23 patients in Group 1 and 13/14 patients in Group 2, but not in patients in Groups 3 or 4. Therefore, KM55 may detect incidental IgA deposition in pediatric patients. Gd-IgA1 may be involved in the pathogenesis of these immune-related diseases; alternatively, KM55 may recognize IgA-related immunocomplexes in a non-specific manner.Shinya IshikoTomoko HorinouchiRika FujimaruYuko ShimaHiroshi KaitoRyojiro TanakaShingo IshimoriAtsushi KondoSadayuki NagaiYuya AotoNana SakakibaraChina NaganoTomohiko YamamuraMomoka YoshimuraKoichi NakanishiJunya FujimuraNaohiro KamiyoshiHiroaki NagaseNorishige YoshikawaKazumoto IijimaKandai NozuNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 10, Iss 1, Pp 1-6 (2020)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Shinya Ishiko
Tomoko Horinouchi
Rika Fujimaru
Yuko Shima
Hiroshi Kaito
Ryojiro Tanaka
Shingo Ishimori
Atsushi Kondo
Sadayuki Nagai
Yuya Aoto
Nana Sakakibara
China Nagano
Tomohiko Yamamura
Momoka Yoshimura
Koichi Nakanishi
Junya Fujimura
Naohiro Kamiyoshi
Hiroaki Nagase
Norishige Yoshikawa
Kazumoto Iijima
Kandai Nozu
Glomerular galactose-deficient IgA1 expression analysis in pediatric patients with glomerular diseases
description Abstract Galactose-deficient IgA1 (Gd-IgA1) is important in the pathogenesis of IgA nephropathy (IgAN). A Gd-IgA1-specific monoclonal antibody (KM55) has revealed glomerular Gd-IgA1 deposition solely in patients with IgAN and IgA vasculitis with nephritis (IgAV-N). However, this specificity is controversial and has not been demonstrated in pediatric patients. Here, we conducted double-immunofluorescence staining of IgA and Gd-IgA1 in 60 pediatric patients with various glomerular diseases. We divided patients into four groups: (1) patients with IgAN and IgAV-N (n = 23); (2) patients with immunocomplex-mediated glomerulonephritis accompanied by IgA deposition, including lupus nephritis, membranoproliferative glomerulonephritis, and membranous nephropathy (n = 14); (3) patients with other glomerular diseases involving IgA deposition, including idiopathic nephrotic syndrome (INS), oligomeganephronia, Alport syndrome, dense deposit disease, and crescentic glomerulonephritis (n = 11); and (4) patients with IgA-negative diseases including INS, membranoproliferative glomerulonephritis, membranous nephropathy, oligomeganephronia, Alport syndrome, C3 glomerulonephritis, poststreptococcal acute glomerulonephritis, and hemolytic uremic syndrome (n = 12). KM55 staining revealed Gd-IgA1-positive findings in 23/23 patients in Group 1 and 13/14 patients in Group 2, but not in patients in Groups 3 or 4. Therefore, KM55 may detect incidental IgA deposition in pediatric patients. Gd-IgA1 may be involved in the pathogenesis of these immune-related diseases; alternatively, KM55 may recognize IgA-related immunocomplexes in a non-specific manner.
format article
author Shinya Ishiko
Tomoko Horinouchi
Rika Fujimaru
Yuko Shima
Hiroshi Kaito
Ryojiro Tanaka
Shingo Ishimori
Atsushi Kondo
Sadayuki Nagai
Yuya Aoto
Nana Sakakibara
China Nagano
Tomohiko Yamamura
Momoka Yoshimura
Koichi Nakanishi
Junya Fujimura
Naohiro Kamiyoshi
Hiroaki Nagase
Norishige Yoshikawa
Kazumoto Iijima
Kandai Nozu
author_facet Shinya Ishiko
Tomoko Horinouchi
Rika Fujimaru
Yuko Shima
Hiroshi Kaito
Ryojiro Tanaka
Shingo Ishimori
Atsushi Kondo
Sadayuki Nagai
Yuya Aoto
Nana Sakakibara
China Nagano
Tomohiko Yamamura
Momoka Yoshimura
Koichi Nakanishi
Junya Fujimura
Naohiro Kamiyoshi
Hiroaki Nagase
Norishige Yoshikawa
Kazumoto Iijima
Kandai Nozu
author_sort Shinya Ishiko
title Glomerular galactose-deficient IgA1 expression analysis in pediatric patients with glomerular diseases
title_short Glomerular galactose-deficient IgA1 expression analysis in pediatric patients with glomerular diseases
title_full Glomerular galactose-deficient IgA1 expression analysis in pediatric patients with glomerular diseases
title_fullStr Glomerular galactose-deficient IgA1 expression analysis in pediatric patients with glomerular diseases
title_full_unstemmed Glomerular galactose-deficient IgA1 expression analysis in pediatric patients with glomerular diseases
title_sort glomerular galactose-deficient iga1 expression analysis in pediatric patients with glomerular diseases
publisher Nature Portfolio
publishDate 2020
url https://doaj.org/article/51582829b5bb434c960fdaccff19cb9f
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