11 research outputs found

    Estimated proportion vaccinated on time by age (months) by vaccine for each geographical region in the Gambia for a) schedule 1 and b) schedule 2.

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    <p>Blue bars: proportion who received BCG on time. Brown bars: proportion who received DPT1 on time. Green bars: proportion who received DPT2 on time. Orange bars: proportion who received DPT3 on time. Turquoise bars: proportion who received measles vaccine on time. Red bars: proportion who received DPT booster on time. Vertical bars: 95% confidence intervals.</p

    DPT3 coverage, GNI and under-5 mortality rate by countries in the AFRO region.

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    <p>Circle size represents size of under-5 mortality rate. (<a href="http://data.worldbank.org/indicator/SH.DYN.MORT" target="_blank">http://data.worldbank.org/indicator/SH.DYN.MORT</a>). Blue circle: WHO estimates for The Gambia. (<a href="http://apps.who.int/immunization_monitoring/globalsummary" target="_blank">http://apps.who.int/immunization_monitoring/globalsummary</a>). Green circle: URR and NBR combined. Grey circle: Western health region. Yellow circle: West Kiang, LRR. GNI: Gross National Income per capita.</p

    General characteristics of the study population and study sites to evaluate the Expanded Programme on Immunisation in the Gambia between January 2005 and December 2012.

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    <p>HDSS: Health and Demographic surveillance system; DSS: demographic surveillance system; KeMRES: Keneba Electronic Medical Records System; EPI: Expanded Programme of Immunisation.</p><p>General characteristics of the study population and study sites to evaluate the Expanded Programme on Immunisation in the Gambia between January 2005 and December 2012.</p

    Proportion of eligible children vaccinated and median age (in months) by vaccine type and by region in The Gambia.

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    <p>Blue bars: proportion who received BCG on time. Brown bars: proportion who received DPT1 on time. Green bars: proportion who received DPT2 on time. Orange bars: proportion who received DPT2 on time. Turquoise bars: proportion who received measles vaccine on time. Red bars: proportion who received DPT booster on time. Blue line: Median age (in months) for BCG. Brown line: Median age (in months) for DPT1. Green line: Median age (in months) for DPT2. Orange line: Median age (in months) for DPT3. Turquoise line: Median age (in months) for measles vaccine. Red line: Median age (in months) for DPT booster. Vertical bars: Interquartilte range in months of age at vaccination.</p

    Map of The Gambia.

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    <p>WCR: Western Coastal Region; LRR: Lower River Region; CRR: Central River Region; URR: Upper River Region. Dashed circles represent the demographic surveillance sites: Farafenni Health and Demographic Surveillance System (FHDSS), Basse Health and Demographic Surveillance System (BHDSS), and Kiang West Demographic surveillance system (KWDSS).</p

    <b>Table 3.</b> Proportion delayed to vaccination and median delay by vaccine type and by geographical region in The Gambia.

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    <p>IQR: Interquartile range in weeks; <sup>1</sup>Median delay estimated from the upper limit of schedule 2 for each vaccine.</p><p><b>Table 3.</b> Proportion delayed to vaccination and median delay by vaccine type and by geographical region in The Gambia.</p

    A schematic diagram of the HIV-1 clade A (HIVA) immunogen.

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    <p>The HIVA protein consists of consensus amino acid sequences of clade A p24 and p17 Gag and a string of partially overlapping CD8<sup>+</sup> T-cell epitopes identified in chronically infected individuals [<a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0078289#B23" target="_blank">23</a>]. Pool P90 of 15-mer peptides overlapping by 11 amino acids across the Gag portion is shown below the protein. Pool P9 consisted of known CD8<sup>+</sup> T-cell epitope peptides derived from the polyepitope region.</p

    MVA.HIVA-elicited weak T-cell responses in fresh IFN-γ ELISPOT assay.

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    <p>The net fresh <i>ex-vivo</i> ELISPOT frequencies of IFN-γ-producing cells (mean of stimulated wells minus mean of negative control wells) to HIVA peptide pools P9 and P90 at all 4 bleed time points for the control (Con) and vaccinated (Vac) groups are shown. The p value for the only statistically significant difference between the two groups after Bonferroni correction is given. The median ‘mock’ no-peptide background response across all wells on plates that passed QC was 5 SFU/10<sup>6</sup> PBMC (IQ range 0-20), and median PHA response was 1,850 SFU/10<sup>6</sup> PBMC (IQ range 1,065- 2,960).</p
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