3 research outputs found

    IL-7R<sup>neg</sup> short-term effector <sub>vs</sub> IL-7R<sup>pos</sup> long-term memory T cells persistance at late time points after primary HCMV infection.

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    <p>Frequencies of IL-7R<sup>pos</sup> T cells in <b>(A-B)</b> total memory and <b>(C-D)</b> HCMV-specific CD4<sup>+</sup> or CD8<sup>+</sup> T cells are reported. Data are from HCMV-seronegative subjects (“No infection”, n = 5, only for total memory), patients (both pregnant and non-pregnant) within 1 month (n = 25) or at 6–12 months (n = 18) after primary infection onset, and subjects with remote infection (n = 10). “HCMV-specific” indicates the sum of the single protein-specific T cells. Each symbol represents an individual and column upper limits indicate median values.</p

    Frequencies of CD4<sup>+</sup> and CD8<sup>+</sup> T cells specific for HCMV proteins IE-1, pp65, gHgLpUL128L (pentamer) and gB in the naĂŻve pool of HCMV-seronegative subjects and in the memory pool of subjects with primary or remote HCMV infection.

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    <p><b>A, B.</b> Frequencies of protein-specific <b>(A)</b> CD4<sup>+</sup> and <b>(B)</b> CD8<sup>+</sup> naïve T cells in 6 HCMV-seronegative subjects are reported. Each symbol represents an individual and horizontal black lines indicate median values. <b>C, D.</b> Frequencies of protein-specific <b>(C)</b> CD4<sup>+</sup> and <b>(D)</b> CD8<sup>+</sup> memory T cells in 6 patients with primary HCMV infection tested within one month and 6–12 months after infection onset. <b>E, F.</b> Frequencies of protein-specific <b>(E)</b> CD4<sup>+</sup> and <b>(F)</b> CD8<sup>+</sup> memory T cells in 7 subjects with remote HCMV infection are reported.</p
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