13 research outputs found

    CD38<sup>+</sup>CD161<sup>lo</sup>Vα7.2<sup>+</sup> cells are inversely associated with age and changes in MAIT cells.

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    <p>A) Spearman correlation of day 2 to day 7 fold changes in %MAIT cells with fold changes across the same days in i) CD161<sup>lo</sup>Vα7.2<sup>+</sup>, and ii) CD38<sup>+</sup>CD161<sup>lo</sup>Vα7.2<sup>+</sup> cells. B) Spearman correlation of CD38<sup>+</sup>CD161<sup>lo</sup>Vα7.2<sup>+</sup> cells with age for i) healthy controls and ii) cholera patients on day 7 after presentation.</p

    Class-switched antibody responses against LPS are correlated with MAIT cell responses.

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    <p>Antibody responses against A) LPS, and B) CtxB, of cholera patients at days 2, 7, and 30 after hospitalization, displayed as mean with standard errors. Compared with day 2, * P<0.05; ** P<0.01; *** P<0.001. Correlation of fold changes in %MAIT cells and fold changes in antibody response against C) LPS, and D) CtxB, of cholera patients.</p

    Plasma and memory B cell responses targeting O-specific polysaccharide (OSP) are associated with protection against <i>Vibrio cholerae</i> O1 infection among household contacts of cholera patients in Bangladesh

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    <div><p>Background</p><p>The mediators of protection against cholera, a severe dehydrating illness of humans caused by <i>Vibrio cholerae</i>, are unknown. We have previously shown that plasma IgA as well as memory B IgG cells targeting lipopolysaccharide (LPS) of <i>Vibrio cholerae</i> O1 correlate with protection against <i>V</i>. <i>cholerae</i> O1 infection among household contacts of cholera patients. Protection against cholera is serogroup specific, and serogroup specificity is defined by the O-specific polysaccharide (OSP) component of LPS. Therefore, we prospectively followed household contacts of cholera patients to determine whether OSP-specific immune responses present at the time of enrollment are associated with protection against <i>V</i>. <i>cholerae</i> infection.</p><p>Methodology</p><p>In this study, we enrolled two hundred forty two household contacts of one hundred fifty index patients who were infected with <i>Vibrio cholerae</i>. We determined OSP-specific memory B cells and plasma IgA, IgG and IgM antibody responses on study entry (day 2).</p><p>Principle findings</p><p>The presence of OSP-specific plasma IgA, IgM, and IgG antibody responses on study entry were associated with a decrease in the risk of infection in household contacts (IgA, p = 0.015; IgM, p = 0.01, and IgG, p = 0.024). In addition, the presence of OSP-specific IgG memory B cell responses in peripheral blood on study entry was also associated with a decreased risk of infection (44% reduction; 95% CI: 31.1 to 99.8) in contacts. No protection was associated with cholera toxin B subunit (CtxB)-specific memory B cell responses.</p><p>Conclusion</p><p>These results suggest that immune responses that target OSP, both in plasma and memory responses, may be important in mediating protection against infection with <i>V</i>. <i>cholerae</i> O1.</p></div
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