Identification of immunological bioprocesses involved in peri‐implantitis using weighted gene co‐expression network analysis

Author:

Chen Liang‐Wen1ORCID,Jin Su‐Han23ORCID,Lu Qian1,Zhou Jian‐Guo4ORCID,Liu Jian‐Guo5,Guan Xiao‐Yan3,Xia Hai‐Bin1,He Hong2

Affiliation:

1. Hubei‐MOST KLOS & KLOBM Department of Oral Implantology School and Hospital of Stomatology Wuhan University Wuhan China

2. Department of Orthodontics Hubei‐MOST KLOS & KLOBM School & Hospital of Stomatology Wuhan University Wuhan China

3. Department of Orthodontics Affiliated Stomatological Hospital of Zunyi Medical University Zunyi China

4. Department of Oncology Affiliated Hospital of Zunyi Medical University Zunyi China

5. School of Stomatology Special Key Laboratory of Oral Diseases Research Higher Education Institution Zunyi Medical University Zunyi China

Abstract

AbstractBackgroundPeri‐implantitis is an irreversible infectious disease that occurs with high incidence. Exploring the immune responses of peri‐implantitis is key to developing targeted treatment strategies. However, there is limited research on the immune response of peri‐implantitis.MethodsThis study performed a weighted gene co‐expression network analysis to identify the peri‐implantitis related gene network and conducted a functional enrichment analysis of the gene network. Thereafter, the candidate hub genes were selected by constructing a protein‐protein interaction network and drawing an upset plot. The hub genes were identified through their significant associations with disease condition and validated using quantitative reverse transcription‐polymerase chain reaction (qRT‐PCR) analysis. Using the gene set variation analysis, the hub genes were further used to explore infiltrating immunocytes and immune factors in peri‐implantitis. Finally, the immunocytes and immune factor related hub genes were intersected to obtain the therapeutic target, which was validated using histological staining.ResultsThe peri‐implantitis related gene network was enriched in innate and adaptive immune response. Subsequently, interleukin (IL)1B, IL10, ITGAM, ITGB1, STAT3, and TLR4 were identified as hub genes. Plasmacytoid dendritic cells, macrophages, myeloid‐derived suppressor cells, natural killer T cells, and immature B cells were positively and significantly related to the hub genes IL1B, TLR4, ITGAM, and ITGB1 (correlation coefficient > 0.80). While immune factors CXCL10, IL6, and CXCL12 and hub genes IL10 and IL1B held the highest degree in the immune factors network. IL1B may be a promising therapeutic target.ConclusionThis study provides new insights into the hub genes, immunocytes, and immune factors underlying peri‐implantitis immunological bioprocess.

Publisher

Wiley

Subject

Periodontics,General Medicine

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3