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        <identifier>oai:figshare.com:article/33827608</identifier>
        <datestamp>2026-09-16T04:31:04Z</datestamp>
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          <dc:title>Data Sheet 1_Circulating Helicobacter pylori extracellular vesicles in serum as biomarkers of infection.pdf</dc:title>
          <dc:creator>María Fernanda González (13945371)</dc:creator>
          <dc:creator>Gabriel Díaz-Serrano (24960430)</dc:creator>
          <dc:creator>Manuel Valenzuela-Valderrama (13945377)</dc:creator>
          <dc:creator>Marcelo J. Kogan (1563130)</dc:creator>
          <dc:creator>Alejandro Corvalán (44828)</dc:creator>
          <dc:creator>Andrew F.G. Quest (5195417)</dc:creator>
          <dc:creator>Lisette Leyton (172553)</dc:creator>
          <dc:subject>Clinical Microbiology</dc:subject>
          <dc:subject>bacterial extracellular vesicles</dc:subject>
          <dc:subject>diagnosis</dc:subject>
          <dc:subject>H. pylori infection</dc:subject>
          <dc:subject>inflammation</dc:subject>
          <dc:subject>UreB</dc:subject>
          <dc:description>&lt;p&gt;Gastric infection by Helicobacter pylori (H. pylori) is associated with extra-gastric pathologies. H. pylori can promote these pathologies by generating extracellular vesicles (Hp-EVs), which cross biological barriers and access other tissues through the circulation. However, the presence of Hp-EVs in the human circulation has not been demonstrated. We isolated and characterized EVs from serum of non-infected and infected patients, and used immunoblots (IB) to identify markers from host cells EVs (h-EVs) and Hp-EVs. We also assessed the predictive capacity of IB with an anti-Urease subunit B (UreB) antibody to identify true positive cases of H. pylori infection. Finally, we compared the diagnostic utility of IB-UreB with other detection methods of H. pylori in blood samples. Thirty symptomatic individuals underwent endoscopy, gastric biopsy and blood tests. Rapid Urease test (RUT), pathological analysis and Gastropanel® (GP) classified 16 cases (53.3%) as H. pylori positive. EV markers CD63 and CD81 were detected in all the isolated EVs from the serum of these patients. Moreover, UreB+ EVs were detected in 62.5% of H. pylori-infected patients, providing the first evidence of circulating Hp-EVs in human serum. Among the blood biomarkers evaluated, IB-UreB+ proved to be the best method for diagnosing H. pylori-positive cases. Furthermore, combining IB-UreB+ with GP increased its diagnostic value. Our findings provide the first evidence of circulating Hp-EVs in human serum, thereby supporting a mechanism for systemic dissemination of bacterial virulence factors. Additionally, their detection in blood samples may enable minimally invasive diagnosis of H. pylori infection.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-16T04:31:04Z</dc:date>
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          <dc:identifier>10.3389/fcimb.2026.1893888.s001</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/Data_Sheet_1_Circulating_Helicobacter_pylori_extracellular_vesicles_in_serum_as_biomarkers_of_infection_pdf/33827608</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
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