Modes of the initiation of T cell-mediated immune responses.

Medical review (Berlin, Germany) Pub Date : 2026-01-20 eCollection Date: 2026-02-01 DOI:10.1515/mr-2025-0066
Long Li, Zhi Yao
{"title":"Modes of the initiation of T cell-mediated immune responses.","authors":"Long Li, Zhi Yao","doi":"10.1515/mr-2025-0066","DOIUrl":null,"url":null,"abstract":"<p><p>T cell-mediated immune response is the center of adaptive immunity. Despite more than five decades of research, the knowledge of mechanisms drives the initiation of T cell-mediated immune response is still limited due to the complexity of T cell-mediated immunity. Based on the accumulating evidences of Th1-mediated immune response, a \"priming-activation\" model was proposed to describe the initiation of the immune response. In this model, naïve CD4 T cells undergo a priming phase in the draining lymph nodes (dLNs) to polarize to Th1 fate by signals from dendritic cells (DCs). The primed Th1 cells then migrate to the antigen-affected loci and encounter antigen presenting cells (APCs) again. With signals from these cells, the primed Th1 cells differentiate to activated effector cells to coordinate Th1-centered immunity, which is the activation phase of Th1-mediated immune response. Recently, a model for the initiation of Th2-mediated immunity has been proposed, which highly resembles the priming-activation model for Th1 cells. We summarize the advances of Th17-mediated immunity and our understanding of it, and propose a two-step model for the initiation of Th17-mediated autoimmune immunity. Our model is similar to the priming-activation model of Th1 cells, as well. Although there are major knowledge gaps on molecular and cellular mechanisms in our model to be addressed, we hope that this model, with the associated gaps being addressed, will provide framework for research on the initiation of Th17-mediated immune responses and eventually enhances our understanding of how T cell-mediated immunity initiates.</p>","PeriodicalId":74151,"journal":{"name":"Medical review (Berlin, Germany)","volume":"6 1","pages":"83-86"},"PeriodicalIF":0.0000,"publicationDate":"2026-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12955352/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Medical review (Berlin, Germany)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1515/mr-2025-0066","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/2/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

T cell-mediated immune response is the center of adaptive immunity. Despite more than five decades of research, the knowledge of mechanisms drives the initiation of T cell-mediated immune response is still limited due to the complexity of T cell-mediated immunity. Based on the accumulating evidences of Th1-mediated immune response, a "priming-activation" model was proposed to describe the initiation of the immune response. In this model, naïve CD4 T cells undergo a priming phase in the draining lymph nodes (dLNs) to polarize to Th1 fate by signals from dendritic cells (DCs). The primed Th1 cells then migrate to the antigen-affected loci and encounter antigen presenting cells (APCs) again. With signals from these cells, the primed Th1 cells differentiate to activated effector cells to coordinate Th1-centered immunity, which is the activation phase of Th1-mediated immune response. Recently, a model for the initiation of Th2-mediated immunity has been proposed, which highly resembles the priming-activation model for Th1 cells. We summarize the advances of Th17-mediated immunity and our understanding of it, and propose a two-step model for the initiation of Th17-mediated autoimmune immunity. Our model is similar to the priming-activation model of Th1 cells, as well. Although there are major knowledge gaps on molecular and cellular mechanisms in our model to be addressed, we hope that this model, with the associated gaps being addressed, will provide framework for research on the initiation of Th17-mediated immune responses and eventually enhances our understanding of how T cell-mediated immunity initiates.

Abstract Image

T细胞介导的免疫应答的启动模式。
T细胞介导的免疫反应是适应性免疫的核心。尽管经过了50多年的研究,但由于T细胞介导免疫的复杂性,对T细胞介导免疫反应启动机制的了解仍然有限。基于对th1介导的免疫应答证据的积累,提出了一种描述免疫应答起始的“启动-激活”模型。在这个模型中,naïve CD4 T细胞在引流淋巴结(dln)中经历一个启动阶段,通过来自树突状细胞(dc)的信号极化到Th1命运。引物Th1细胞然后迁移到受抗原影响的位点,再次遇到抗原提呈细胞(APCs)。通过这些细胞发出的信号,被激活的Th1细胞分化为激活的效应细胞,协调以Th1为中心的免疫,这是Th1介导的免疫应答的激活阶段。最近,th2介导的免疫启动模型被提出,该模型与Th1细胞的启动激活模型非常相似。我们总结了th17介导免疫的研究进展及其认识,并提出了th17介导自身免疫启动的两步模型。我们的模型也类似于Th1细胞的启动激活模型。虽然我们的模型在分子和细胞机制方面存在重大的知识空白,但我们希望这个模型,随着相关空白的解决,将为研究th17介导的免疫反应的启动提供框架,并最终增强我们对T细胞介导的免疫如何启动的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
1.30
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书