25 research outputs found

    Prevalence of helminth infections.

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    <p>The prevalence of helminth infections is displayed for all infections together, as well as the subgroups intestinal helminth infections and filariases, and for each individual infection.</p

    Study flow.

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    <p>Study flow displaying the inclusion of study participants. Patients were included in the main analysis if they provided at least 2 stool and urine samples and one blood sample. Patients were included for subanalyses if they provided at least 2 stool samples (intestinal helminths), 2 urine samples (<i>S</i>. <i>haematobium</i>) or 1 blood sample (filariases). </p

    Participant flow diagram.

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    <p>Randomisation and flow of participants over a period of 6 months for adults (cohorts 1 to 5), adolescents (cohort 6; 13–17 years), and children (cohort 7; 6–12 years). Similar dose groups are matched with shading (light grey, 3 × 10<sup>6</sup> PFU; dark grey, 2 × 10<sup>7</sup> PFU). GP, glycoprotein; ELISA, enzyme-linked immunosorbent assay; PFU, plaque-forming units; rVSV, recombinant vesicular stomatitis virus.</p

    Viral load in saliva for children and adolescents.

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    <p>rVSV<b>Δ</b>G-ZEBOV-GP (rVSV) RNA copy numbers in saliva presented as log10 rVSV RNA copies/ml from day 2 and 7 (d2 and d7) post-injection in adolescents and children vaccinated with 2 × 10<sup>7</sup> PFU. The broken line denotes the limit of quantitation, and the dotted line denotes the limit of detection. About 67% (12/18) and 30% (6/20) adolescents and children, respectively, had samples above the limit of quantification at day 7. *P < 0.05; **P < 0.01.PFU, plaque-forming units.</p
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