Registration for a live webinar on 'Precision medicine treatment for anticancer drug resistance' is now open.
See webinar detailsWe noted you are experiencing viewing problems
-
Check with your IT department that JWPlatform, JWPlayer and Amazon AWS & CloudFront are not being blocked by your network. The relevant domains are *.jwplatform.com, *.jwpsrv.com, *.jwpcdn.com, jwpltx.com, jwpsrv.a.ssl.fastly.net, *.amazonaws.com and *.cloudfront.net. The relevant ports are 80 and 443.
-
Check the following talk links to see which ones work correctly:
Auto Mode
HTTP Progressive Download Send us your results from the above test links at access@hstalks.com and we will contact you with further advice on troubleshooting your viewing problems. -
No luck yet? More tips for troubleshooting viewing issues
-
Contact HST Support access@hstalks.com
-
Please review our troubleshooting guide for tips and advice on resolving your viewing problems.
-
For additional help, please don't hesitate to contact HST support access@hstalks.com
We hope you have enjoyed this limited-length demo
This is a limited length demo talk; you may
login or
review methods of
obtaining more access.
Printable Handouts
Navigable Slide Index
- Introduction
- Importance of innate immunity in the gut
- Mucosal tissues of the human body
- Intestinal pathogens and human disease
- Mucosal immune system: distinctive features
- Gut-associated lymphoid tissue (GALT)
- Structure of the GALT: small intestine
- Structure of the GALT: large intestine
- Mucus forms a key protective barrier in the gut
- Mucus secretion increases during infection
- Antimicrobial proteins protect the epithelium
- Epithelial cell transcytosis of secretory IgA
- Functions of secretory IgA
- Uptake and transport of antigen by M cells
- Microbial sensing regulates intestinal homeostasis
- Sensing of microbes occurs through PRR
- Innate immune signaling (1)
- Innate immune signaling (2)
- PRR signals in IEC
- MyD88 signals in IEC
- Control of inflammatory responses in the intestine
- Intestinal macrophages are anti-inflammatory
- Intestinal DC 'conditioning'
- Inflammatory bowel disease (IBD)
- Genome-wide association studies
- The enigma of NOD2 and Crohn's disease
- NOD2 signaling in response to bacterial MDP
- NOD2 signaling in IEC
- NOD2 signaling regulates myeloid cell function
- Autophagy also regulates IEC and myeloid cells
- Innate immune activation in IBD pathogenesis
- Innate intestinal inflammation, MyD88 dependent
- MyD88 activation drives intestinal inflammation
- Haematopoeitic MyD88 signals
- Immune dysregulation in chronic inflammation
- Innate lymphoid cells (ILC) drive innate IBD
- ILC provide early innate immune protection
- Additional distinct functional subsets of ILC
- Leukocyte populations and intestinal homeostasis
- Summary
- Acknowledgements
Topics Covered
- Mucosal tissues of the human body
- Intestinal pathogens
- Mucosal immune system: distinctive features
- Gut-associated lymphoid tissue (GALT)
- Structure of the GALT: small and large intestine
- Mucus, a key protective barrier
- Antimicrobial proteins protect the epithelium
- Epithelial cell transcytosis of secretory IgA
- Uptake and transport of antigen by M cells
- Microbial sensing regulates intestinal homeostasis
- Sensing of microbes occurs through PRR
- MyD88 signals in IEC
- Intestinal macrophages are anti-inflammatory
- Intestinal DC 'conditioning'
- Inflammatory bowel disease (IBD)
- Genome-wide association studies
- The enigma of NOD2 and Crohn's disease
- NOD2 signaling in response to bacterial MDP
- NOD2 signaling regulates myeloid cell function
- Autophagy also regulates IEC and myeloid cells
- MyD88 activation drives intestinal inflammation
- Haematopoeitic MyD88 signals
- Immune dysregulation in chronic inflammation
- Innate lymphoid cells (ILC) drive innate IBD
- Leukocyte populations and intestinal homeostasis
Links
Series:
Categories:
Therapeutic Areas:
Talk Citation
Maloy, K. (2013, January 31). Innate immunity in the intestine in health and disease [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved December 21, 2024, from https://doi.org/10.69645/GTRZ4965.Export Citation (RIS)
Publication History
Financial Disclosures
- Prof. Kevin Maloy has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.
A selection of talks on Immunology
Transcript
Please wait while the transcript is being prepared...
0:00
Hi. My name's Kevin Maloy.
I'm a lecturer in
Experimental Pathology at
the Sir William Dunn
School of Pathology
at the University of Oxford.
My lab has a long-standing
interest in mucosal immunology,
with a particular focus on
the regulation of innate
immunity in the intestine,
which is the subject
of this lecture.
My group is interested in
how different types of
innate immune
receptors contribute
to protection from infection,
but also to immune pathology
and allergen testing.
I'll use some examples from
our research to illustrate
some recent advances in the innate
immune pathways in the intestine.
0:34
I will briefly describe some of
the key features of
intestinal immunity,
including some of the
unique characteristics that
differentiate the
intestinal immune system
from the systemic immune system.
I'll then outline
the key functions
of intestinal epithelial cells,
which are an integral part of
innate immune
defense in the gut,
by maintaining an
effective barrier function
and by producing
protective immune factors.
I will also consider
how intestinal microbes
are detected by the innate
immune system through
pattern recognition
receptors (PPRs),
and how these interactions
can regulate intestinal
homeostasis.
I will outline recent
findings on the types
and functions of innate
leukocytes in the gut.
In the second part
of the lecture,
I will discuss how dysregulation
of innate immunity in
the gut is associated with
inflammatory bowel disease.
1:17
Most of what we know about how
the immune system works has been
derived from extensive study
of systemic immune responses,
which are elicited in the
peripheral lymphoid tissues,
such as the lymph
nodes and spleen.
However, most pathogens
invade the body at interfaces
between the host and
external environment,
such as in mucosal surfaces.
These are internal
body surfaces lined
by a thin layer of
mucus-secreting epithelium,
such as the
gastrointestinal tract,
the respiratory tract and
the urogenital tract.
These surfaces constitute
a huge surface area.
Therefore, the
mucosal immune system
is the largest immune
compartment in the body.
It contains 75 percent
of all lymphocytes
and produces the
majority of antibodies.
The mucosal immune system
presents the first line of defense
against invading pathogens,
and also provides protection
against reinfection
by previously
encountered pathogens.