Cargando…

Association of IL6 and IL10 gene promotor polymorphisms with susceptibility to acute necrotizing encephalopathy

OBJECTIVE: Acute necrotizing encephalopathy (ANE) is a severe complication of infectious diseases affecting the brain and systemic organs. The main pathogenesis is cytokine storm, in which interleukin-6 (IL-6) and interleukin-10 (IL-10) are candidates for key cytokines. To further elucidate their ro...

Descripción completa

Detalles Bibliográficos
Autores principales: Hoshino, Ai, Takahashi, Naoto, Oka, Akira, Mizuguchi, Masashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10435083/
https://www.ncbi.nlm.nih.gov/pubmed/37600000
http://dx.doi.org/10.3389/fnins.2023.1231957
_version_ 1785092048772136960
author Hoshino, Ai
Takahashi, Naoto
Oka, Akira
Mizuguchi, Masashi
author_facet Hoshino, Ai
Takahashi, Naoto
Oka, Akira
Mizuguchi, Masashi
author_sort Hoshino, Ai
collection PubMed
description OBJECTIVE: Acute necrotizing encephalopathy (ANE) is a severe complication of infectious diseases affecting the brain and systemic organs. The main pathogenesis is cytokine storm, in which interleukin-6 (IL-6) and interleukin-10 (IL-10) are candidates for key cytokines. To further elucidate their roles in the etiology and pathogenesis of ANE, we studied polymorphisms in the promotor regions of the IL6 and IL10 genes by genetic and functional analyses. METHODS: We first conducted a case–control association study of four IL6 and three IL10 polymorphisms. We genotyped 31 Japanese ANE cases and compared the results with those of approximately 200 Japanese controls. For the two polymorphisms showing a possible association, we next studied whether the polymorphisms alter the production of IL-6 or IL-10 by lymphoblasts upon phorbol 12-myristate 13-acetate (PMA) stimulation. RESULTS: The frequencies of IL6 rs1800796G allele and IL10 rs1800871/rs1800872 CC/CC diplotype were significantly higher in ANE cases than in controls. The IL10 CC/CC diplotype was associated with low IL-10 production, whereas the IL6 GG genotype was not associated with IL-6 production. CONCLUSION: IL10 rs1800871/rs1800872 CC/CC diplotype may predispose Japanese children to ANE by altering IL-10 production in the early phase of infection. Etio-pathogenetic significance of IL6 rs1800796G remains to be elucidated.
format Online
Article
Text
id pubmed-10435083
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-104350832023-08-18 Association of IL6 and IL10 gene promotor polymorphisms with susceptibility to acute necrotizing encephalopathy Hoshino, Ai Takahashi, Naoto Oka, Akira Mizuguchi, Masashi Front Neurosci Neuroscience OBJECTIVE: Acute necrotizing encephalopathy (ANE) is a severe complication of infectious diseases affecting the brain and systemic organs. The main pathogenesis is cytokine storm, in which interleukin-6 (IL-6) and interleukin-10 (IL-10) are candidates for key cytokines. To further elucidate their roles in the etiology and pathogenesis of ANE, we studied polymorphisms in the promotor regions of the IL6 and IL10 genes by genetic and functional analyses. METHODS: We first conducted a case–control association study of four IL6 and three IL10 polymorphisms. We genotyped 31 Japanese ANE cases and compared the results with those of approximately 200 Japanese controls. For the two polymorphisms showing a possible association, we next studied whether the polymorphisms alter the production of IL-6 or IL-10 by lymphoblasts upon phorbol 12-myristate 13-acetate (PMA) stimulation. RESULTS: The frequencies of IL6 rs1800796G allele and IL10 rs1800871/rs1800872 CC/CC diplotype were significantly higher in ANE cases than in controls. The IL10 CC/CC diplotype was associated with low IL-10 production, whereas the IL6 GG genotype was not associated with IL-6 production. CONCLUSION: IL10 rs1800871/rs1800872 CC/CC diplotype may predispose Japanese children to ANE by altering IL-10 production in the early phase of infection. Etio-pathogenetic significance of IL6 rs1800796G remains to be elucidated. Frontiers Media S.A. 2023-08-03 /pmc/articles/PMC10435083/ /pubmed/37600000 http://dx.doi.org/10.3389/fnins.2023.1231957 Text en Copyright © 2023 Hoshino, Takahashi, Oka and Mizuguchi. https://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 Neuroscience
Hoshino, Ai
Takahashi, Naoto
Oka, Akira
Mizuguchi, Masashi
Association of IL6 and IL10 gene promotor polymorphisms with susceptibility to acute necrotizing encephalopathy
title Association of IL6 and IL10 gene promotor polymorphisms with susceptibility to acute necrotizing encephalopathy
title_full Association of IL6 and IL10 gene promotor polymorphisms with susceptibility to acute necrotizing encephalopathy
title_fullStr Association of IL6 and IL10 gene promotor polymorphisms with susceptibility to acute necrotizing encephalopathy
title_full_unstemmed Association of IL6 and IL10 gene promotor polymorphisms with susceptibility to acute necrotizing encephalopathy
title_short Association of IL6 and IL10 gene promotor polymorphisms with susceptibility to acute necrotizing encephalopathy
title_sort association of il6 and il10 gene promotor polymorphisms with susceptibility to acute necrotizing encephalopathy
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10435083/
https://www.ncbi.nlm.nih.gov/pubmed/37600000
http://dx.doi.org/10.3389/fnins.2023.1231957
work_keys_str_mv AT hoshinoai associationofil6andil10genepromotorpolymorphismswithsusceptibilitytoacutenecrotizingencephalopathy
AT takahashinaoto associationofil6andil10genepromotorpolymorphismswithsusceptibilitytoacutenecrotizingencephalopathy
AT okaakira associationofil6andil10genepromotorpolymorphismswithsusceptibilitytoacutenecrotizingencephalopathy
AT mizuguchimasashi associationofil6andil10genepromotorpolymorphismswithsusceptibilitytoacutenecrotizingencephalopathy