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The Expression of Glycoprotein Genes in the Inflammatory Process of Kawasaki Disease

Background: Kawasaki disease (KD) is the most common form of febrile coronary vasculitis disease to occur in children. Early diagnosis and proper therapy can prevent the complication of coronary artery lesions (CAL). The main pathogenesis of KD is an inflammatory process related to the host's g...

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Autores principales: Kuo, Kuang-Che, Yang, Ya-Ling, Lo, Mao-Hung, Cai, Xin-Yuan, Kuo, Ho-Chang, Huang, Ying-Hsien
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7744457/
https://www.ncbi.nlm.nih.gov/pubmed/33344384
http://dx.doi.org/10.3389/fped.2020.592122
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author Kuo, Kuang-Che
Yang, Ya-Ling
Lo, Mao-Hung
Cai, Xin-Yuan
Kuo, Ho-Chang
Huang, Ying-Hsien
author_facet Kuo, Kuang-Che
Yang, Ya-Ling
Lo, Mao-Hung
Cai, Xin-Yuan
Kuo, Ho-Chang
Huang, Ying-Hsien
author_sort Kuo, Kuang-Che
collection PubMed
description Background: Kawasaki disease (KD) is the most common form of febrile coronary vasculitis disease to occur in children. Early diagnosis and proper therapy can prevent the complication of coronary artery lesions (CAL). The main pathogenesis of KD is an inflammatory process related to the host's genetic characteristics. In innate human immunity, the interaction of leukocytes and glycoprotein plays an important role against microbes. The purpose of our study was to understand the role of leukocytes' glycoprotein genes during the acute phase of KD. Materials and Methods: We enrolled a total of 97 subjects from a medical center. Of those, 24 subjects were healthy controls, and 24 subjects were fever controls; the other 49 subjects were KD patients who had had blood samples taken both before and after IVIG treatment. We collected the total RNA from leukocytes and performed a quantitative polymerase chain reaction for the HP, GRP84, and CLEC4D genes in real time. Results: Compared with both the healthy and fever controls, the upregulation of HP, GRP84, and CLEC4D genes was significant in peripheral leukocytes during acute-phase KD. The transcriptional level of these respective genes not only demonstrated a positive correlation with each other, but were also effective predictors for KD (all auROC >0.87) according to the ROC curve analysis. The hyper-expression of these three genes was significantly associated with IVIG resistance, but not CAL formation. Conclusions: Our study demonstrates that the expression of HP, GRP84, and CLEC4D genes of leukocytes play an important role in the pathogenesis and primary IVIG response during the acute inflammatory process of KD.
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spelling pubmed-77444572020-12-18 The Expression of Glycoprotein Genes in the Inflammatory Process of Kawasaki Disease Kuo, Kuang-Che Yang, Ya-Ling Lo, Mao-Hung Cai, Xin-Yuan Kuo, Ho-Chang Huang, Ying-Hsien Front Pediatr Pediatrics Background: Kawasaki disease (KD) is the most common form of febrile coronary vasculitis disease to occur in children. Early diagnosis and proper therapy can prevent the complication of coronary artery lesions (CAL). The main pathogenesis of KD is an inflammatory process related to the host's genetic characteristics. In innate human immunity, the interaction of leukocytes and glycoprotein plays an important role against microbes. The purpose of our study was to understand the role of leukocytes' glycoprotein genes during the acute phase of KD. Materials and Methods: We enrolled a total of 97 subjects from a medical center. Of those, 24 subjects were healthy controls, and 24 subjects were fever controls; the other 49 subjects were KD patients who had had blood samples taken both before and after IVIG treatment. We collected the total RNA from leukocytes and performed a quantitative polymerase chain reaction for the HP, GRP84, and CLEC4D genes in real time. Results: Compared with both the healthy and fever controls, the upregulation of HP, GRP84, and CLEC4D genes was significant in peripheral leukocytes during acute-phase KD. The transcriptional level of these respective genes not only demonstrated a positive correlation with each other, but were also effective predictors for KD (all auROC >0.87) according to the ROC curve analysis. The hyper-expression of these three genes was significantly associated with IVIG resistance, but not CAL formation. Conclusions: Our study demonstrates that the expression of HP, GRP84, and CLEC4D genes of leukocytes play an important role in the pathogenesis and primary IVIG response during the acute inflammatory process of KD. Frontiers Media S.A. 2020-12-03 /pmc/articles/PMC7744457/ /pubmed/33344384 http://dx.doi.org/10.3389/fped.2020.592122 Text en Copyright © 2020 Kuo, Yang, Lo, Cai, Kuo and Huang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pediatrics
Kuo, Kuang-Che
Yang, Ya-Ling
Lo, Mao-Hung
Cai, Xin-Yuan
Kuo, Ho-Chang
Huang, Ying-Hsien
The Expression of Glycoprotein Genes in the Inflammatory Process of Kawasaki Disease
title The Expression of Glycoprotein Genes in the Inflammatory Process of Kawasaki Disease
title_full The Expression of Glycoprotein Genes in the Inflammatory Process of Kawasaki Disease
title_fullStr The Expression of Glycoprotein Genes in the Inflammatory Process of Kawasaki Disease
title_full_unstemmed The Expression of Glycoprotein Genes in the Inflammatory Process of Kawasaki Disease
title_short The Expression of Glycoprotein Genes in the Inflammatory Process of Kawasaki Disease
title_sort expression of glycoprotein genes in the inflammatory process of kawasaki disease
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7744457/
https://www.ncbi.nlm.nih.gov/pubmed/33344384
http://dx.doi.org/10.3389/fped.2020.592122
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