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Anti-Hexokinase 1 Antibody as a Novel Serum Biomarker of a Subgroup of Diabetic Macular Edema

Diabetic retinopathy (DR) induces the breakdown of the blood-retinal barrier and promotes neuroinflammation, although autoimmune responses to sequestered retinal antigens remain poorly understood. In this study, we investigated the autoantibodies for retinal antigens in sera from diabetic macular ed...

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Autores principales: Yoshitake, Tatsuya, Murakami, Tomoaki, Yoshitake, Shin, Suzuma, Kiyoshi, Dodo, Yoko, Fujimoto, Masahiro, Ito, Shinji, Tsujikawa, Akitaka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6423027/
https://www.ncbi.nlm.nih.gov/pubmed/30886155
http://dx.doi.org/10.1038/s41598-019-39777-z
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author Yoshitake, Tatsuya
Murakami, Tomoaki
Yoshitake, Shin
Suzuma, Kiyoshi
Dodo, Yoko
Fujimoto, Masahiro
Ito, Shinji
Tsujikawa, Akitaka
author_facet Yoshitake, Tatsuya
Murakami, Tomoaki
Yoshitake, Shin
Suzuma, Kiyoshi
Dodo, Yoko
Fujimoto, Masahiro
Ito, Shinji
Tsujikawa, Akitaka
author_sort Yoshitake, Tatsuya
collection PubMed
description Diabetic retinopathy (DR) induces the breakdown of the blood-retinal barrier and promotes neuroinflammation, although autoimmune responses to sequestered retinal antigens remain poorly understood. In this study, we investigated the autoantibodies for retinal antigens in sera from diabetic macular edema (DME) patients. Screening by immunoblotting demonstrated that IgG from 7 of 10 DME sera samples reacted to an ~102-kDa autoantigen from porcine retinas. Immunoprecipitation with autoantibodies from DME sera and subsequent mass spectrometry enabled us to identify hexokinase 1 as an autoantigen reactive to IgG from DME sera. IgG in 7 of 10 DME sera partially colocalized to hexokinase 1 in the outer plexiform layer of rodent retinas. Quantitative analyses using enzyme-linked immunosorbent assays revealed that the serum titers of this autoantibody were significantly higher in the DME sera than those in the sera from diabetic patients without DME, and 20 (24.1%) of the 83 DME serum samples had higher IgG titers than the cutoff value (mean + 2 standard deviations of the sera from diabetic patients without DR). Multivariate logistic regression analysis confirmed that the higher titer of anti-hexokinase 1 IgG was clinically feasible for the diagnosis of DME. These data identify anti-hexokinase 1 antibody as a serum biomarker of a subset of DME.
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spelling pubmed-64230272019-03-26 Anti-Hexokinase 1 Antibody as a Novel Serum Biomarker of a Subgroup of Diabetic Macular Edema Yoshitake, Tatsuya Murakami, Tomoaki Yoshitake, Shin Suzuma, Kiyoshi Dodo, Yoko Fujimoto, Masahiro Ito, Shinji Tsujikawa, Akitaka Sci Rep Article Diabetic retinopathy (DR) induces the breakdown of the blood-retinal barrier and promotes neuroinflammation, although autoimmune responses to sequestered retinal antigens remain poorly understood. In this study, we investigated the autoantibodies for retinal antigens in sera from diabetic macular edema (DME) patients. Screening by immunoblotting demonstrated that IgG from 7 of 10 DME sera samples reacted to an ~102-kDa autoantigen from porcine retinas. Immunoprecipitation with autoantibodies from DME sera and subsequent mass spectrometry enabled us to identify hexokinase 1 as an autoantigen reactive to IgG from DME sera. IgG in 7 of 10 DME sera partially colocalized to hexokinase 1 in the outer plexiform layer of rodent retinas. Quantitative analyses using enzyme-linked immunosorbent assays revealed that the serum titers of this autoantibody were significantly higher in the DME sera than those in the sera from diabetic patients without DME, and 20 (24.1%) of the 83 DME serum samples had higher IgG titers than the cutoff value (mean + 2 standard deviations of the sera from diabetic patients without DR). Multivariate logistic regression analysis confirmed that the higher titer of anti-hexokinase 1 IgG was clinically feasible for the diagnosis of DME. These data identify anti-hexokinase 1 antibody as a serum biomarker of a subset of DME. Nature Publishing Group UK 2019-03-18 /pmc/articles/PMC6423027/ /pubmed/30886155 http://dx.doi.org/10.1038/s41598-019-39777-z Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Yoshitake, Tatsuya
Murakami, Tomoaki
Yoshitake, Shin
Suzuma, Kiyoshi
Dodo, Yoko
Fujimoto, Masahiro
Ito, Shinji
Tsujikawa, Akitaka
Anti-Hexokinase 1 Antibody as a Novel Serum Biomarker of a Subgroup of Diabetic Macular Edema
title Anti-Hexokinase 1 Antibody as a Novel Serum Biomarker of a Subgroup of Diabetic Macular Edema
title_full Anti-Hexokinase 1 Antibody as a Novel Serum Biomarker of a Subgroup of Diabetic Macular Edema
title_fullStr Anti-Hexokinase 1 Antibody as a Novel Serum Biomarker of a Subgroup of Diabetic Macular Edema
title_full_unstemmed Anti-Hexokinase 1 Antibody as a Novel Serum Biomarker of a Subgroup of Diabetic Macular Edema
title_short Anti-Hexokinase 1 Antibody as a Novel Serum Biomarker of a Subgroup of Diabetic Macular Edema
title_sort anti-hexokinase 1 antibody as a novel serum biomarker of a subgroup of diabetic macular edema
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6423027/
https://www.ncbi.nlm.nih.gov/pubmed/30886155
http://dx.doi.org/10.1038/s41598-019-39777-z
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