Related Experiment Video
Updated: May 5, 2026

07:25
Stem Cell-Derived Viral Ag-Specific T Lymphocytes Suppress HBV Replication in Mice
Published on: September 25, 2019
6.6K
Early T helper cell programming of gene expression in human
Soile Tuomela1, Riitta Lahesmaa
1Turku Centre for Biotechnology, University of Turku and Åbo Akademi University, Tykistökatu 6, 20520 Turku, Finland.
Seminars in Immunology
|November 20, 2013
Summary
Understanding human T helper cell differentiation is crucial. This review highlights studies using human cells, comparing them with mouse models to identify knowledge gaps in T cell priming mechanisms.
Area of Science:
- Immunology
- Cellular Biology
- Molecular Mechanisms
Background:
- Naïve T helper cell differentiation into effector cells is a key area of immunology research.
- Current knowledge heavily relies on mouse models, with limited data from human primary cells.
- Human cells are the definitive model for human immunology and are increasingly analyzable with modern technologies.
Purpose of the Study:
- To review studies on human primary cells elucidating T helper cell subtype priming mechanisms.
- To emphasize recent high-throughput studies in this field.
- To compare human and mouse studies, identifying research gaps in human cell-based investigations.
Main Methods:
- Review of existing literature on human primary cell studies.
- Focus on high-throughput studies.
- Comparative analysis of human and mouse T helper cell differentiation research.
Main Results:
- An overview of the current status of human primary cell studies in T helper cell differentiation.
- Identification of specific areas where human primary cell research is lacking compared to mouse models.
- Highlighting the importance of parallel human and mouse studies for translational research.
Conclusions:
- Human primary cells are essential for understanding human immunology, despite the prevalence of mouse models.
- Further research using human cells is needed to fully elucidate T helper cell priming mechanisms.
- Comparative studies are vital for validating mouse model findings in human contexts.
Keywords:
ChIA-PETChIPChIP-seqEpigeneticsGenome-wideHigh-throughputHumanRNA interferenceRNA-seqRNAiSNPSTATT cell receptorT helper cellTCRTfhThTranscriptionUTRchromatin immunoprecipitationchromatin immunoprecipitation coupled to high-throughput sequencingchromatin interaction analysis by paired-end tag sequencingfollicular T helper cellhigh-throughput RNA sequencingiTreginducible T regulatory cell, adaptive T regulatorylincRNAlncRNAlong intergenic non-coding RNAlong non-coding RNAmiRNAmicroRNAshort interfering RNAsiRNAsignal transducer and activator of transcriptionsingle nucleotide polymorphismuntranslated region of mRNARelated Concept Videos
T Cell Activation and Clonal Selection
13.7K
T cells are integral to our adaptive immune system, recognizing and effectively responding to foreign antigens. T cell activation and clonal selection are pivotal in orchestrating this immune response. This article elucidates these mechanisms, detailing the roles of cluster of differentiation (CD) markers, major histocompatibility complex (MHC) molecules, costimulatory signals, and the process of clonal selection.
Naive T cells that have not yet encountered an antigen express two primary CD...
Naive T cells that have not yet encountered an antigen express two primary CD...
13.7K
T Cell Types and Functions
3.2K
When T cells with CD4 markers are activated, they give rise to two types of effector cells: helper T cells and regulatory T cells. Meanwhile, T cells with CD8 markers differentiate into effector cytotoxic T cells. The differentiation of CD4 T cells into helper T cell subsets, such as Th1, Th2, and Th17 cells, is dependent on the antigen type, antigen-presenting cell, and regulatory cytokines.
Th1 cells stimulate dendritic cells to express necessary co-stimulatory molecules on their surfaces for...
Th1 cells stimulate dendritic cells to express necessary co-stimulatory molecules on their surfaces for...
3.2K

