• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

基于深度学习的自身免疫性疾病预测

Deep learning-based prediction of autoimmune diseases.

作者信息

Yang Donghong, Peng Xin, Zheng Senlin, Peng Shenglan

机构信息

School of Information Engineering, Jingdezhen Ceramic University, Jingdezhen, 333403, China.

Third Institute of Oceanography, Ministry of Natural Resources, Xiamen, 361005, China.

出版信息

Sci Rep. 2025 Feb 7;15(1):4576. doi: 10.1038/s41598-025-88477-4.

DOI:10.1038/s41598-025-88477-4
PMID:39920178
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11806040/
Abstract

Autoimmune Diseases are a complex group of diseases caused by the immune system mistakenly attacking body tissues. Their etiology involves multiple factors such as genetics, environmental factors, and abnormalities in immune cells, making prediction and treatment challenging. T cells, as a core component of the immune system, play a critical role in the human immune system and have a significant impact on the pathogenesis of autoimmune diseases. Several studies have demonstrated that T-cell receptors (TCRs) may be involved in the pathogenesis of various autoimmune diseases, which provides strong theoretical support and new therapeutic targets for the prediction and treatment of autoimmune diseases. This study focuses on the prediction of several autoimmune diseases mediated by T cells, and proposes two models: one is the AutoY model based on convolutional neural networks, and the other is the LSTMY model, a bidirectional LSTM network model that integrates the attention mechanism. Experimental results show that both models exhibit good performance in the prediction of the four autoimmune diseases, with the AutoY model performing slightly better in comparison. In particular, the average area under the ROC curve (AUC) of the AutoY model exceeded 0.93 in the prediction of all the diseases, and the AUC value reached 0.99 in two diseases, type 1 diabetes and multiple sclerosis. These results demonstrate the high accuracy, stability, and good generalization ability of the two models, which makes them promising tools in the field of autoimmune disease prediction and provides support for the use of the TCR bank for the noninvasive detection of autoimmune disease non-invasive detection is supported.

摘要

自身免疫性疾病是由免疫系统错误地攻击身体组织而引起的一组复杂疾病。其病因涉及多种因素,如遗传因素、环境因素和免疫细胞异常,这使得预测和治疗具有挑战性。T细胞作为免疫系统的核心组成部分,在人体免疫系统中发挥着关键作用,对自身免疫性疾病的发病机制有重大影响。多项研究表明,T细胞受体(TCRs)可能参与各种自身免疫性疾病的发病机制,这为自身免疫性疾病的预测和治疗提供了有力的理论支持和新的治疗靶点。本研究聚焦于几种由T细胞介导的自身免疫性疾病的预测,并提出了两种模型:一种是基于卷积神经网络的AutoY模型,另一种是整合了注意力机制的双向LSTM网络模型LSTMY。实验结果表明,这两种模型在四种自身免疫性疾病的预测中均表现出良好的性能,相比之下,AutoY模型表现略优。特别是,AutoY模型在所有疾病预测中的ROC曲线下面积(AUC)平均值超过0.93,在1型糖尿病和多发性硬化症这两种疾病中AUC值达到0.99。这些结果证明了这两种模型具有高准确性、稳定性和良好的泛化能力,使其成为自身免疫性疾病预测领域有前景的工具,并为使用TCR库进行自身免疫性疾病的无创检测提供了支持。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/278c/11806040/eed234b42d10/41598_2025_88477_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/278c/11806040/0a6014e1d45b/41598_2025_88477_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/278c/11806040/dfdc07993f4d/41598_2025_88477_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/278c/11806040/709dcebb0f2b/41598_2025_88477_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/278c/11806040/9847708d714a/41598_2025_88477_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/278c/11806040/cf134bc3b8b5/41598_2025_88477_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/278c/11806040/4c3c917cd49f/41598_2025_88477_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/278c/11806040/aa73cd92b58e/41598_2025_88477_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/278c/11806040/5ecbeb497d8b/41598_2025_88477_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/278c/11806040/eed234b42d10/41598_2025_88477_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/278c/11806040/0a6014e1d45b/41598_2025_88477_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/278c/11806040/dfdc07993f4d/41598_2025_88477_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/278c/11806040/709dcebb0f2b/41598_2025_88477_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/278c/11806040/9847708d714a/41598_2025_88477_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/278c/11806040/cf134bc3b8b5/41598_2025_88477_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/278c/11806040/4c3c917cd49f/41598_2025_88477_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/278c/11806040/aa73cd92b58e/41598_2025_88477_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/278c/11806040/5ecbeb497d8b/41598_2025_88477_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/278c/11806040/eed234b42d10/41598_2025_88477_Fig9_HTML.jpg

相似文献

1
Deep learning-based prediction of autoimmune diseases.基于深度学习的自身免疫性疾病预测
Sci Rep. 2025 Feb 7;15(1):4576. doi: 10.1038/s41598-025-88477-4.
2
Therapeutic intervention in autoimmunity.自身免疫性疾病的治疗干预。
Behring Inst Mitt. 1994 Jul(94):171-8.
3
TITAN: T-cell receptor specificity prediction with bimodal attention networks.TITAN:基于双模态注意力网络的 T 细胞受体特异性预测。
Bioinformatics. 2021 Jul 12;37(Suppl_1):i237-i244. doi: 10.1093/bioinformatics/btab294.
4
Antigen-specific T cells in autoimmune diseases with a focus on multiple sclerosis and experimental allergic encephalomyelitis.自身免疫性疾病中抗原特异性T细胞,重点关注多发性硬化症和实验性变应性脑脊髓炎。
Cell Mol Life Sci. 1999 Oct 1;56(1-2):5-21. doi: 10.1007/s000180050002.
5
Autoimmune pathogenesis of multiple sclerosis: role of autoreactive T lymphocytes and new immunotherapeutic strategies.多发性硬化症的自身免疫发病机制:自身反应性T淋巴细胞的作用及新的免疫治疗策略。
Crit Rev Immunol. 1997;17(1):33-75. doi: 10.1615/critrevimmunol.v17.i1.20.
6
Limited heterogeneity of autoantigens and T cells in autoimmune diseases?自身免疫性疾病中自身抗原和T细胞的异质性有限?
Res Immunol. 1991 Jun-Aug;142(5-6):487-90. doi: 10.1016/0923-2494(91)90053-l.
7
The recognition of self-antigens and autoimmune disease.自身抗原的识别与自身免疫性疾病。
Curr Opin Immunol. 1991 Feb;3(1):22-5. doi: 10.1016/0952-7915(91)90071-8.
8
[Molecular mimicry in the etiology of autoimmune diseases].[自身免疫性疾病病因中的分子模拟]
Postepy Hig Med Dosw (Online). 2012 Jul 13;66:475-91. doi: 10.5604/17322693.1003484.
9
Construction of Risk Prediction Model of Type 2 Diabetic Kidney Disease Based on Deep Learning.基于深度学习的 2 型糖尿病肾病风险预测模型的构建。
Diabetes Metab J. 2024 Jul;48(4):771-779. doi: 10.4093/dmj.2023.0033. Epub 2024 Apr 30.
10
Time-Dependent Deep Learning Prediction of Multiple Sclerosis Disability.多发性硬化症残疾的时间依赖性深度学习预测
J Imaging Inform Med. 2024 Dec;37(6):3231-3249. doi: 10.1007/s10278-024-01031-y. Epub 2024 Jun 13.

本文引用的文献

1
Innate and adaptive immune abnormalities underlying autoimmune diseases: the genetic connections.自身免疫性疾病的先天和适应性免疫异常:遗传关联。
Sci China Life Sci. 2023 Jul;66(7):1482-1517. doi: 10.1007/s11427-021-2187-3. Epub 2023 Feb 3.
2
Multiple instance neural networks based on sparse attention for cancer detection using T-cell receptor sequences.基于稀疏注意力的多实例神经网络用于 T 细胞受体序列的癌症检测。
BMC Bioinformatics. 2022 Nov 8;23(1):469. doi: 10.1186/s12859-022-05012-2.
3
Preclinical Autoimmune Disease: a Comparison of Rheumatoid Arthritis, Systemic Lupus Erythematosus, Multiple Sclerosis and Type 1 Diabetes.
临床前自身免疫性疾病:类风湿关节炎、系统性红斑狼疮、多发性硬化症和1型糖尿病的比较
Front Immunol. 2022 Jun 30;13:899372. doi: 10.3389/fimmu.2022.899372. eCollection 2022.
4
DeepLION: Deep Multi-Instance Learning Improves the Prediction of Cancer-Associated T Cell Receptors for Accurate Cancer Detection.DeepLION:深度多实例学习改进癌症相关T细胞受体预测以实现准确的癌症检测。
Front Genet. 2022 Apr 11;13:860510. doi: 10.3389/fgene.2022.860510. eCollection 2022.
5
SARS-CoV-2 (COVID-19)-specific T cell and B cell responses in convalescent rheumatoid arthritis: Monozygotic twins pair case observation.康复期类风湿关节炎患者中 SARS-CoV-2(COVID-19)特异性 T 细胞和 B 细胞应答:同卵双胞胎配对病例观察。
Scand J Immunol. 2022 May;95(5):e13151. doi: 10.1111/sji.13151. Epub 2022 Mar 2.
6
The similarity of class II HLA genotypes defines patterns of autoreactivity in idiopathic bone marrow failure disorders.Ⅱ类 HLA 基因型的相似性定义了特发性骨髓衰竭疾病中自身反应的模式。
Blood. 2021 Dec 30;138(26):2781-2798. doi: 10.1182/blood.2021012900.
7
A comparative study of multiple instance learning methods for cancer detection using T-cell receptor sequences.使用T细胞受体序列进行癌症检测的多实例学习方法的比较研究
Comput Struct Biotechnol J. 2021 May 24;19:3255-3268. doi: 10.1016/j.csbj.2021.05.038. eCollection 2021.
8
Corrigendum: Adult-Onset Anti-Citrullinated Peptide Antibody-Negative Destructive Rheumatoid Arthritis Is Characterized by a Disease-Specific CD8+ T Lymphocyte Signature.勘误:成人起病的抗瓜氨酸化肽抗体阴性的破坏性类风湿关节炎具有疾病特异性的CD8 + T淋巴细胞特征。
Front Immunol. 2021 May 31;12:710831. doi: 10.3389/fimmu.2021.710831. eCollection 2021.
9
The Prevalence of Rheumatoid Arthritis: A Systematic Review of Population-based Studies.类风湿关节炎的患病率:基于人群的研究的系统评价。
J Rheumatol. 2021 May;48(5):669-676. doi: 10.3899/jrheum.200367. Epub 2020 Oct 15.
10
De novo prediction of cancer-associated T cell receptors for noninvasive cancer detection.用于非侵入性癌症检测的癌症相关T细胞受体的从头预测。
Sci Transl Med. 2020 Aug 19;12(557). doi: 10.1126/scitranslmed.aaz3738.