V<i>γ</i>4+ T Cells: A Novel IL-17-Producing <i>γδ</i> T Subsets during the Early Phase of Chlamydial Airway Infection in Mice

<div>V<i>γ</i>1+ T and V<i>γ</i>4+ T cell proliferated and activated during Cm respiratory infection. Mononuclear cells in lung tissues at different time points postinfection were extracted. Staining with anti-mouse CD3, TCR<i>γδ</i>, TCRV<i>γ</i>1, and TCRV<i>γ</i>4 antibody to analyze the percentage and absolute number of TCRV<i>γ</i>1+ TCR<i>γδ</i>+ T cells (a) and TCRV<i>γ</i>4<sup>+</sup>TCR<i>γδ</i><sup>+</sup>T cells (b) by flow cytometry. The activation extent of V<i>γ</i>1+ T (c) and V<i>γ</i>4+ T (d) cell was measured by the expression of CD69, staining with anti-mouse CD69 antibody. 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Mediators of Inflammation

fig3

Figure 3

Figure 3: V<i>γ</i>4+ T Cells: A Novel IL-17-Producing <i>γδ</i> T Subsets during the Early Phase of Chlamydial Airway Infection in Mice 

Mediators of Inflammation

Vγ4+ T Cells: A Novel IL-17-Producing γδ T Subsets during the Early Phase of Chlamydial Airway Infection in Mice

Figure 3