Development of small molecules as anti-inflammatory and anti-resorptive drugs
dc.contributor.advisor
van t' Hof, Rob
en
dc.contributor.advisor
Ralston, Stuart
en
dc.contributor.author
Coste, Emmanuel
en
dc.contributor.sponsor
Principality of Monaco
en
dc.contributor.sponsor
Modern Biosciences
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dc.date.accessioned
2015-02-17T15:42:35Z
dc.date.available
2015-02-17T15:42:35Z
dc.date.issued
2011-07-05
dc.description.abstract
Rheumatoid arthritis is an auto-immune inflammatory disease that leads to
stiff and swollen joints. Patients also have severe bone destruction of the affected
joints and another common symptom of rheumatoid arthritis is a generalised bone
loss that can lead to osteoporosis. Currently, there are many treatments for
rheumatoid arthritis, which provide a recession of the inflammatory symptoms.
However, none of these treatments are able to provide a complete protection against
the rheumatoid arthritis-induced bone loss. Furthermore, the most effective available
treatments such as glucocorticoids or the new biological drugs are not optimal since
they either cause severe side effects or are very expensive and difficult to produce.
Hence, there is a real need for new cost-effective treatments that can act on both
inflammation and bone loss symptoms of rheumatoid arthritis. ABD compounds are
small molecules, relatively easy to synthesize at reasonable cost. In this thesis, I
discuss the effects of these small molecules on both rheumatoid arthritis-induced
inflammation and bone loss.
Daily treatments with the ketones ABD328 and ABD345, or with the
sulphonamide ABD455 prevent inflammation in an animal model of rheumatoid
arthritis. Furthermore, micro-CT and histology analysis showed that these treatments
also provide a reliable protection against bone destruction of affected joints and
generalised bone loss. In vitro data showed that this protective effect on bone was
osteoclast specific. Indeed, Ishow here that treatment of other bone cells (such as
osteoblasts or macrophages) with ABD compounds does not affect their biology.
The mechanism of action of these compounds has also been studied and I
show here that ABD compounds inhibit both inflammation and osteoclastogenesis by
inhibiting the signalling pathways that are activated in response to pro-inflammatory
cytokines such as TNF . This work led to the design and synthesis of further improved compounds,
such as ABD599, that are currently considered as very interesting candidates for
clinical trials.
In conclusion, the ABD compounds, as small cost-effective molecules,
represent a novel class of rheumatoid arthritis treatments by acting on both
inflammation and bone loss symptoms of the disease.
en
dc.identifier.uri
http://hdl.handle.net/1842/9941
dc.language.iso
en
dc.publisher
The University of Edinburgh
en
dc.relation.hasversion
Wakkach,A., Mansour,A., Dacquin,R., Coste,E., Jurdic,P., Carle,G.F., and Blin- Wakkach,C. (2008). Bone marrow microenvironment controls the in vivo differentiation of murine dendritic cells into osteoclasts. Blood 112, 5074-5083.
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dc.subject
ABD compounds
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dc.subject
rheumatoid arthritis
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dc.title
Development of small molecules as anti-inflammatory and anti-resorptive drugs
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dc.type
Thesis or Dissertation
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dc.type.qualificationlevel
Doctoral
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dc.type.qualificationname
PhD Doctor of Philosophy
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