The human intestine contains about 1014 micro-organisms that critically
contribute to
tissue homeostasis, host metabolism and other benefi cial processes.
Despite a continuous
microbial exposure within in the intestine, the mucosal immune system is
able to
maintain a state of tolerance to the microbiota. An aberrant immune
response of the
intestinal immune system results in a defective tolerance in the
intestine, which leads to
a breakdown of intestinal homeostasis. This in turn, can lead to chronic
intestinal infl ammation
or inflammatory bowel disease (IBD).
From an immunological perspective, exaggerated responses by mucosal T and
B cells
(the adaptive immune system) have traditionally been regarded as the key
contributors
to the pathogenesis of IBD. However, discoveries of innate defects that
are associated
with IBD have refocused the attention to this arm of the immune system.
In this thesis we try to answer some of the open questions concerning the
pathogenesis
of IBD and defects in the innate immune system.
http://repub.eur.nl/res/pub/20711/100915_Lierop%2C%20Petrus%20Paulus%20Elisabeth%20van.pdf
http://repub.eur.nl/res/pub/20711/100915_Lierop%2C%20Petrus%20Paulus%20Elisabeth%20van.pdf
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