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Printable Handouts
Navigable Slide Index
- Introduction
- Self-tolerance: a definition
- Why understand tolerance mechanisms?
- Knowledge of self-tolerance
- Why do we not react to self?
- Self-tolerance is acquired rather than inherited
- Classical transplantation tolerance
- Central tolerance by clonal deletion
- Central tolerance
- T-cell tolerance
- What constitutes a self-antigen for T-cell tolerance?
- T-cell tolerance in the thymus
- Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy
- Regulatory T-cells
- Ipex syndrome
- Two major sets of CD4+ regulatory T-cells
- Role of thymus in T-cell development
- Evidence for clonal deletion in B-cells
- Peripheral tolerance
- Peripheral tolerance in T-cells
- Overview
- Co-stimulation
- Co-inhibition
- Lack of co-stimulation can result in tolerance
- Short-term co-receptor or co-stimulation blockade can promote tolerance
- Inter T-cell co-operation/Licensing of dendritic cells
- Lack of inter T-cell co-operation promotes tolerance induction
- Outcomes to tolerant cells
- Mechanisms learned from experimental tolerance induction in “adult” mice
- Tolerance to (danger-free) human gamma globulin in mice
- High dose and low dose tolerance
- B-cells stay unresponsive as long as T-cells remain tolerant: helplessness
- Autoimmune diseases
- How may tolerance “fail”
- T-cell bypass (for some autoimmune diseases)
- Coreceptor blockade to induce tolerance to foreign proteins in mice
- Non depleting CD4 and CD8 antibodies produce tolerance
- The foxp3 gene is needed for tolerance in TCR transgenic mice
- TGFβ signalling in T-cells is required for transplant tolerance through blindfolding
- Tolerance depends on constant vigilance by Foxp3+ Treg
- Tolerised mice show linked-suppression
- Tolerance through co-receptor blockade is dominant and infectious
- Decommissioning of dendritic cells by regulatory T-cells
- Acquired tissue privilege
- Modern immunosuppression: tipping the balance
Topics Covered
- Introduction to self-tolerance
- Molecular basis of tolerance
- Central and peripheral tolerance
- Autoimmune diseases
- Co-stimulation and co-inhibition
- Experimental tolerance induction
Links
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Talk Citation
Waldmann, H. (2020, October 29). Self-tolerance [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved November 21, 2024, from https://doi.org/10.69645/ZXBB3769.Export Citation (RIS)
Publication History
Financial Disclosures
- Herman Waldman has ownership interests in the Absolute Antibody company.
Other Talks in the Series: The Immune System - Key Concepts and Questions
Transcript
Please wait while the transcript is being prepared...
0:00
I'm Herman Waldmann from the Dunn School of Pathology, University of Oxford,
and I'm going to talk to you about tolerance to self.
0:09
The first way I can define self-tolerance is the physiological state where
the immune system does not react destructively
towards "self," and perhaps I would add, even when provoked.
0:22
Why is it important to understand tolerance mechanisms?
Why am I giving this lecture?
Well, it's important that we understand how
the immune system breaks through the mechanism that stops it reacting to self.
Because if know that,
you know what you have to do to make vaccines work.
You know what you have to do to generate the best immunity against cancer.
It gives us understanding also of how tolerance
may be broken when some people get autoimmune disease.
What goes wrong in diabetes?
What goes wrong in multiple sclerosis?
How did it break? Because when we know how it broke,
then we can offer,
perhaps, more precise treatments.
How it can cancer evade immunity?
Now that's a big area that has flourished in the last few years,
and I have written a chapter on which I refer
you to because I'm not going to be able to cover it today.
But it's quite clear that cancers can produce novel proteins,
foreign proteins, and yet the immune system somehow doesn't realize that they're there.
So how is cancer operating to behave as if
tolerant or to make the immune system behave as if tolerant?
If we want to cure autoimmunity,
instead of giving immunosuppressive drugs,
we want to understand what went wrong with tolerance in case
we could reprogram the system again to get it right.
When people overreact and produce hypersensitivity,
allergic reactions, why are they doing that and how can we reduce that?
If we can work out how to regulate that more effectively,
then we will be doing well.
Finally, it's a big goal in transplantation to hijack
the tolerance mechanisms so we don't have to give
so many nasty drugs that penalize the immune system when we don't need to.