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Printable Handouts
Navigable Slide Index
- Introduction
- T cell differentiation (1)
- T cell differentiation (2)
- CD4 T cell subsets in the periphery
- Other players in the immune system
- Cytokines drive T helper subset differentiation in vitro
- Th1 and Th2 development
- Th1 cells clear intracellular pathogens
- Effects of Th2 cytokines during helminth infection
- Lineage transcription factors
- Discovery of a novel cytokine: IL-17
- The emerging concept of a novel CD4 T cell subset
- The combined action of TGFβ and IL-6 is needed for differentiation of Th17 cells
- Th17 cells produce IL-22: driven by the environmental sensor AHR
- IL-17 stimulates and amplifies the innate response against pathogens
- Chronic mucocutaneous Candida – a result of compromised IL-17 responses
- Th1 versus Th17 differentiation
- Effector T cell subset competition
- T follicular helper (TFH) cells
- TFH development
- Effector T cell response regulation (1)
- Effector T cell response regulation (2)
- Regulatory T cells continue to undergo modifications once in the periphery
- Treg function is severely compromised in Foxp3 mutants
- Treg have specialised functions in different environments
- Peripheral CD4 T cell subsets
- Plasticity in effector T cell development
- Identification of IL-17A producing cells
- Th17 cells develop by cross-talk with bacteria in the small intestine
- YFP reporter detection in mice
- EAE: a mouse model for human multiple sclerosis is driven by Th17 cells
- Double producers of IL-17 and IFNγ are common in inflamed tissue
- Cytokines in EAE are preferentially produced by Th17 and ex-Th17 cells
- Extensive Th17 cell plasticity in EAE contributes to enhanced plasticity
- Pathogenic and beneficial aspects
- Th2 plasticity in the face of a strong viral stimulus
- Effector T cell plasticity
- Conclusions
- Acknowledgements
Topics Covered
- CD4 T cell effector specialisation in the periphery
- Influence of cytokines and transcription factors
- Th1 and Th2 paradigm extended with new subsets Treg, Th17 and Tfh
- Plasticity of effector functions
- Functional consequences of plasticity
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Talk Citation
Stockinger, B. (2020, October 29). CD4 T cell subsets [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved December 21, 2024, from https://doi.org/10.69645/FYLX2959.Export Citation (RIS)
Publication History
Financial Disclosures
- Dr. Brigitta Stockinger has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.
Other Talks in the Series: The Immune System - Key Concepts and Questions
Transcript
Please wait while the transcript is being prepared...
0:00
My name is Brigitta Stockinger and I'm
a group leader at The Francis Crick Institute in London.
I'm going to talk about CD4 T cell subsets today.
0:13
T cells are born in the thymus,
which is an organ just above the heart.
They undergo a series of differentiation steps in this organ
and important checkpoints that ascertain they are functionally relevant.
There are two types of T cells made in the thymus that are CD4 T cells,
named such by the co-receptor CD4 on their surface,
or a CD8 T cells named after a CD8 co-receptor.
CD8 T cells are cytotoxic T cells that kill virus infected target.
But today we're focusing on CD4 T cells,
which are much more complex.
They leave the thymus as mature CD4 T cells
in two flavors they either have a regulatory phenotype.
The abbreviation for that here is Treg or they are called T helper cells.
When they enter lymphoid organs in the periphery,
they experienced contact with antigen and
contact with cytokines released from other cell type,
and this shapes the further effector cell differentiation into the subset I listed here,
classic Th1, Th2 later on,
Th17, T follicular helper cells, and iTreg.