Current Understanding of Host Genetics of Otitis Media

The pathogenesis of otitis media (OM), an inflammatory disease of the middle ear (ME), involves interplay between many different factors, including the pathogenicity of infectious pathogens, host immunological status, environmental factors, and genetic predisposition, which is known to be a key dete...

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Main Authors: Ruishuang Geng, Qingzhu Wang, Eileen Chen, Qing Yin Zheng
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-02-01
Series:Frontiers in Genetics
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fgene.2019.01395/full
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spelling doaj-cff0ac6a5ebf4da0ae139b776787f6652020-11-25T02:04:15ZengFrontiers Media S.A.Frontiers in Genetics1664-80212020-02-011010.3389/fgene.2019.01395508988Current Understanding of Host Genetics of Otitis MediaRuishuang Geng0Qingzhu Wang1Qingzhu Wang2Eileen Chen3Qing Yin Zheng4College of Special Education, Binzhou Medical University, Yantai, ChinaCollege of Special Education, Binzhou Medical University, Yantai, ChinaDepartment of Otolaryngology, Guangdong Second Provincial General Hospital, Guangzhou, ChinaDepartment of Otolaryngology, Case Western Reserve University, Cleveland, OH, United StatesDepartment of Otolaryngology, Case Western Reserve University, Cleveland, OH, United StatesThe pathogenesis of otitis media (OM), an inflammatory disease of the middle ear (ME), involves interplay between many different factors, including the pathogenicity of infectious pathogens, host immunological status, environmental factors, and genetic predisposition, which is known to be a key determinant of OM susceptibility. Animal models and human genetics studies have identified many genes and gene variants associated with OM susceptibility: genes that encode components of multiple signaling pathways involved in host immunity and inflammatory responses of the ME mucosa; genes involved in cellular function, such as mucociliary transport, mucin production, and mucous cell metaplasia; and genes that are essential for Eustachian tube (ET) development, ME cavitation, and homeostasis. Since our last review, several new mouse models with mutations in genes such as CCL3, IL-17A, and Nisch have been reported. Moreover, genetic variants and polymorphisms in several genes, including FNDC1, FUT2, A2ML1, TGIF1, CD44, and IL1-RA variable number tandem repeat (VNTR) allele 2, have been identified as being significantly associated with OM. In this review, we focus on the current understanding of the role of host genetics in OM, including recent discoveries and future research prospects. Further studies on the genes identified thus far and the discovery of new genes using advanced technologies such as gene editing, next generation sequencing, and genome-wide association studies, will advance our understanding of the molecular mechanism underlying the pathogenesis of OM and provide new avenues for early screening and developing effective preventative and therapeutic strategies to treat OM.https://www.frontiersin.org/article/10.3389/fgene.2019.01395/fullotitis mediageneticssusceptibilityimmunityinflammatory responsehost
collection DOAJ
language English
format Article
sources DOAJ
author Ruishuang Geng
Qingzhu Wang
Qingzhu Wang
Eileen Chen
Qing Yin Zheng
spellingShingle Ruishuang Geng
Qingzhu Wang
Qingzhu Wang
Eileen Chen
Qing Yin Zheng
Current Understanding of Host Genetics of Otitis Media
Frontiers in Genetics
otitis media
genetics
susceptibility
immunity
inflammatory response
host
author_facet Ruishuang Geng
Qingzhu Wang
Qingzhu Wang
Eileen Chen
Qing Yin Zheng
author_sort Ruishuang Geng
title Current Understanding of Host Genetics of Otitis Media
title_short Current Understanding of Host Genetics of Otitis Media
title_full Current Understanding of Host Genetics of Otitis Media
title_fullStr Current Understanding of Host Genetics of Otitis Media
title_full_unstemmed Current Understanding of Host Genetics of Otitis Media
title_sort current understanding of host genetics of otitis media
publisher Frontiers Media S.A.
series Frontiers in Genetics
issn 1664-8021
publishDate 2020-02-01
description The pathogenesis of otitis media (OM), an inflammatory disease of the middle ear (ME), involves interplay between many different factors, including the pathogenicity of infectious pathogens, host immunological status, environmental factors, and genetic predisposition, which is known to be a key determinant of OM susceptibility. Animal models and human genetics studies have identified many genes and gene variants associated with OM susceptibility: genes that encode components of multiple signaling pathways involved in host immunity and inflammatory responses of the ME mucosa; genes involved in cellular function, such as mucociliary transport, mucin production, and mucous cell metaplasia; and genes that are essential for Eustachian tube (ET) development, ME cavitation, and homeostasis. Since our last review, several new mouse models with mutations in genes such as CCL3, IL-17A, and Nisch have been reported. Moreover, genetic variants and polymorphisms in several genes, including FNDC1, FUT2, A2ML1, TGIF1, CD44, and IL1-RA variable number tandem repeat (VNTR) allele 2, have been identified as being significantly associated with OM. In this review, we focus on the current understanding of the role of host genetics in OM, including recent discoveries and future research prospects. Further studies on the genes identified thus far and the discovery of new genes using advanced technologies such as gene editing, next generation sequencing, and genome-wide association studies, will advance our understanding of the molecular mechanism underlying the pathogenesis of OM and provide new avenues for early screening and developing effective preventative and therapeutic strategies to treat OM.
topic otitis media
genetics
susceptibility
immunity
inflammatory response
host
url https://www.frontiersin.org/article/10.3389/fgene.2019.01395/full
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