<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/CINECAstyle.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-09-24T17:28:48Z</responseDate><request verb="GetRecord" identifier="oai:iris.unica.it:11584/266627" metadataPrefix="oai_dc">https://iris.unica.it/oai/request</request><GetRecord><record><header><identifier>oai:iris.unica.it:11584/266627</identifier><datestamp>2022-10-14T21:40:16Z</datestamp><setSpec>com_11584_207615</setSpec><setSpec>com_11584_111066</setSpec><setSpec>col_11584_265854</setSpec></header><metadata><oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
<dc:title>An integrated top-down and bottom-up&#xd;
proteomic platform to reveal potential salivary&#xd;
biomarkers of the rare disorders SAPHO&#xd;
syndrome, Wilson’s disease and Hereditary&#xd;
angioedema</dc:title>
<dc:creator>SANNA, MONICA</dc:creator>
<dc:subject>angioedema ereditario</dc:subject>
<dc:subject>biomarcatori</dc:subject>
<dc:subject>hereditary angioedema</dc:subject>
<dc:subject>mass spectrometry</dc:subject>
<dc:subject>morbo di Wilson</dc:subject>
<dc:subject>saliva</dc:subject>
<dc:subject>sapho syndrome</dc:subject>
<dc:subject>spettrometria di massa</dc:subject>
<dc:subject>wilson's desease</dc:subject>
<dc:subject>Settore BIO/10 - Biochimica</dc:subject>
<dc:description>Wilson’s disease, SAPHO syndrome and Hereditary angioedema are three rare&#xd;
disorders characterized by a wide spectrum of different clinical manifestations,&#xd;
which involve several organs and apparatus, making the diagnosis extremely&#xd;
difficult. In this study, the salivary proteome and peptidome of subjects affected&#xd;
by these pathologies has been investigated using mass spectrometry, through&#xd;
an integrated top-down and bottom-up platform, and compared with groups of&#xd;
healthy controls, with the aim to assess whether qualitative and quantitative&#xd;
variations of salivary proteins and peptides could be associated to the immune&#xd;
derangement distinctive of each disease and in order to have suggestions on&#xd;
potential specific salivary biomarkers.&#xd;
The analysis of the salivary proteome from patients affected by Wilson’s disease&#xd;
allowed to characterize new oxidized proteoforms of S100A8 and S100A9 and&#xd;
two fragments of the polymeric immunoglobulin receptor named ASVD and&#xd;
AVAD. Higher levels of these proteins and peptides observed in the patients&#xd;
are most likely connected to the oxidative stress, the activation of the&#xd;
inflammatory processes, and the hepatic damage caused by the altered copper&#xd;
transport and its subsequent accumulation in the organism, which is at the&#xd;
origin of the pathology. The observed increase of the level of α-defensins 2 and&#xd;
4 may give a contribution to the development of the disease by the&#xd;
improvement of the free copper.&#xd;
The proteome of patients affected by SAPHO syndrome revealed a significant&#xd;
decrease of cystatins, histatins, and aPRPs, which are involved in the protection&#xd;
against infections, suggesting a reduced ability of these subjects to contrast&#xd;
bacteria colonization, in particular P. acnes which is a possible trigger of this&#xd;
disease. In particular, the lower levels of histatins and the higher frequency of&#xd;
S100A12 observed in patients with respect to controls, may be connected with&#xd;
the dysregulation of the innate immunity and the neutrophil response typical of&#xd;
SAPHO syndrome. Cystatin SN abundance decrease correlated with the disease&#xd;
duration, suggesting its reduced production during the chronic phase of the&#xd;
~ 5 ~&#xd;
disease, while histatins showed positive correlation with serum levels of the C&#xd;
reactive protein.&#xd;
In saliva of Hereditary angioedema patients, the increased percentage of&#xd;
peptides generated by the proteolytic cleavage by metalloproteinases indicates&#xd;
the intense metalloproteinase activity possibly connected to the activation of&#xd;
inflammatory pathways. Interestingly, in consideration of the possible role of&#xd;
cystatin B in enhancing the production of nitric oxide, and the higher salivary&#xd;
levels measured in the patients, we suggest that cystatin B may give a&#xd;
contribution to the vasodilatation and the vasopermeability responsible for the&#xd;
oedema formation, which is the main feature of this pathology.&#xd;
In conclusion, the results obtained in these studies clearly highlighted that the&#xd;
salivary proteome showed some features specific of the three pathologies. Even&#xd;
though these results have been obtained in a small cohort of patients, due to the&#xd;
difficult recruitment of subjects affected by rare disorders, and need further&#xd;
validation by using orthogonal techniques, they strongly suggest that saliva,&#xd;
with easy and non-invasive collection characteristics, could be a biofluid suitable for diagnostic applications.</dc:description>
<dc:date>2016-03-11</dc:date>
<dc:type>info:eu-repo/semantics/doctoralThesis</dc:type>
<dc:identifier>http://hdl.handle.net/11584/266627</dc:identifier>
<dc:language>eng</dc:language>
<dc:relation>numberofpages:119</dc:relation>
<dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
<dc:publisher>Università degli Studi di Cagliari</dc:publisher>
<dc:rights>license:Non specificato</dc:rights>
</oai_dc:dc></metadata></record></GetRecord></OAI-PMH>