(A) Graphic data show percentage numbers of T cells capable of producing IL-22 or IL-17 de novo in the blood (left) and BAL fluid (right) during M. tuberculosis infection. The cells were directly measured by ICS in the presence of CD28/CD49d but without in vitro Ag stimulation. This would allow direct evaluation of regulatory effect by Vγ2Vδ2 T effector cells in the presence or absence of HMBPP. Data are mean percentage numbers in CD3 T cells with error bars of SEM derived from nine cynomolgus macaques. Data were gated on CD3 although most IL-22 cells were CD4 T cells (Fig. S1). This would allow direct comparisons with Vγ2Vδ2 T cells within CD3 T-cell population as shown in Figs. 3–5. CD3+ T cells producing IL-22 or IL-17 in this and other figures included Vγ2Vδ2 T cells. The magnitude of increase in IL-22+ T cells in PBL (^#) at weeks 4, 6 and 8 and in BAL fluid at week 8 were significantly greater than that in IL-17+ T cells (*) (P<0.005). ^# or *, P<0.05, **, P<0.01, ^### or ***, P<0.001. (B) Bar graphic data show that appreciable numbers of IL-22-producing T cells directly measured in medium alone were comparable with those detected in medium plus CD28/CD49d mAbs or in medium plus CD3/CD28 mAbs. Data were mean ± SEM from PBMC obtained at necropsy (8 weeks after infection) from nine cynomolgus macaques. Similar data were seen at weeks 4 and 6 after M. tuberculosis infection. Data were gated on lymphocytes. (C) Representative flow-cytometry histograms of intracellular cytokine staining analysis show that IL-22- and IL-17-producing T cells appear to be two distinct cell populations. The percentage numbers of IL-22 (bottom, right), IL-17 (top, left) producing T cells and IL-22/IL-17 co-expressing T cells (top, right) in CD3 T cells are marked in the individual histograms. Data are CD3 gated. Similar data were repeatedly seen from at least 15 monkeys in blood (n = 21), BAL fluid (n = 21), lung (n = 15), spleen (n = 17), mesenteric lymph node (n = 20). (D) Bar graphic data show percentage numbers of T cells capable of producing IL-22 (left) and IL-17 (right) within CD3+ T cells in lymphocytes isolated from blood, BAL fluid, lungs, spleens and lymph nodes (LN) at 8 weeks after M. tuberculosis infection. Data are mean ± SEM derived from up to 16 macaques' lungs (n = 15, rhesus), spleens (n = 16, rhesus), mesenteric lymph nodes (n = 16, rhesus), blood (n = 9, cynomolgus), and BAL fluid (n = 9, cynomolgus). Data were measured by the ICS without antigen re-stimulation in the presence of medium plus CD28/CD49d mAb. Similar numbers of these cells were detected by the ICS in the presence of medium only (data not shown). Data were gated on CD3. *, P<0.05, **, P<0.01, ***, P<0.001. All rhesus macaques included for all the figures are Chinese rhesus macaques.

Cells from different compartments were either un-stimulated (CD28/CD49d) or stimulated with HMBPP (HMBPP plus CD28/CD49d), and then subjected to intracellular cytokine staining. Blood and BALF were taken at the endpoint matching necropsy schedule after M. tuberculosis infection. (A) Shown on the top panel are representative flow-cytometry histograms of intracellular cytokine staining analysis. The percentage numbers of IL-22-producing T cells in lymphocytes are marked above individual histograms. The bottom-panel flow-cytometry histograms show that HMBPP activation resulted in a reduction in numbers of T cells capable of producing IL-22. The numbers in parentheses denote folds of reduction (ratio of numbers of IL-22-producing T cells from unstimulated versus HMBPP stimulated measurements) after HMBPP treatment. Data were gated on CD3. The flow histograms were from representative M. tuberculosis-infected macaque CN7234 (blood), CN7222 (BAL fluid), RH7716 (lung), RH7717 (spleen) and RH7720 (mesenteric LN) respectively. CN (cynomolgus macaque). (B) Comparative analyses of IL-22-producing T cells in the presence and absence of HMBPP stimulation. Data are mean percentage numbers ± SEM derived from macaque animals' blood (n = 7, cynomolgus), BAL fluids (n = 5, cynomolgus), lungs (n = 7, rhesus), spleens (n = 11, rhesus) and mesenteric lymph nodes (n = 8, rhesus). *, P<0.05, **, P<0.01. Data were gated on CD3. (C) Bar graphic data show percentages (left) and folds (right) of down-regulation of IL-22-producing T cells after HMBPP stimulation. The fold of down-regulation was defined the same as above in Fig. 3A. The percentages of down-regulation were calculated by the formula [(Unstimulated–HMBPP-stimulated)/Unstimulated × 100%]. Results were shown as mean ± SEM. Data were gated on CD3. (D) Comparative analyses of IL-17-producing T cells in the presence and absence of HMBPP stimulation. Data are mean percentage numbers ± SEM derived from macaque animals' blood (n = 9, cynomolgus), BAL fluids (n = 9, cynomolgus), lungs (n = 15, rhesus), spleens (n = 16, rhesus) and mesenteric lymph nodes (n = 20, rhesus). Data were gated on CD3.

Cells from different anatomic compartments were either un-stimulated or stimulated with HMBPP, HMBPP + anti-IFNγ neutralizing Ab, or HMBPP + isotype matched IgG Ab, and then subjected to intracellular cytokine staining. (A) Representative flow-cytometry histograms from monkey RH7717 (lung), RH7719 (spleen) and RH7720 (mesenteric lymph node) show intracellular cytokine staining data demonstrating that anti-IFNγ neutralizing Ab but not isotype IgG reversed the HMBPP-mediated down-regulation of IL-22+CD3+ T cells in lymphocytes from lungs, spleens and mesenteric lymph nodes (LN). Cells were gated on CD3. Percentage numbers of CD3 T cells are listed above individual histograms. (B) Comparative flow-cytometry data show that anti-IFNγ Ab but not isotype IgG reversed the HMBPP-mediated down-regulation of IL-22+CD3+ T cells in lymphocytes from lungs, spleens and mesenteric lymph nodes (LN). Data were mean ± SEM derived from rhesus macaque animals' lungs (n = 7), spleens (n = 9) and mesenteric lymph nodes (n = 14). *, P<0.05, **, P<0.01. Addition of exogenous IFNγ to PBMC culture was not able to activate/expand Vγ2Vδ2 T cells or to down-regulate mature IL-22-producing T cells (data not shown).

(A) Representative confocal microscopic images (63× numerical aperture) at the middle and bottom panels show CD3+IL-22+ T cells (marked by yellow arrows) in lung tissue sections prepared from the right middle lung lobes at 8 weeks after M. tuberculosis infection in rhesus monkeys. The images at the top panel show that no IL-22 (white arrows) was detectable in CD3 T cells in the peri-bronchiolar lymphoid lung section derived from healthy macaques that received BCG vaccination 4 years before. Bar: 5 um. (B) Confocal imaging analyses show percentage numbers of IL-22-producing T cells in the CD3+ T cells in right middle and caudal lung lobe tissues from infected rhesus macaques and undetectable numbers of these cells in lung sections from healthy BCG-vaccinated macaques. Shown are mean percentage numbers in CD3+ T cells calculated from three M. tuberculosis-infected macaques and three healthy BCG vaccinated controls (see Methods). IL-22-producing T cells and IL-22 negative CD3+ T cells were counted from at least 20 confocal-section images in each of six different tissue sections from each macaque; the data from three macaques were then calculated for means, SEM, and p values. No IL-22 staining with very low background-level fluorescence was observed when using control isotype IgG and the antibody non-reactive with tissue-sectioning IL-22 (Data not shown). (C) Representative single-color immunohistochemistry imaging (x400) shows that IL-22-producing T cells (brown) were distributed in granuloma from the right caudle lung lobe (infection site) of one infected rhesus macaque (animal RH 7734, right). Similar staining data were seen in the lung sections from other M. tuberculosis-infected macaques. No IL-22-producing T cells were detectable in lung tissues from healthy BCG vaccinated rhesus macaques (representative animal RH 27097, left). RH (Chinese rhesus macaque).

(A) Representative paired flow-cytometry histograms from monkey RH7406 (lung), RH7720 (spleen), RH7357 (mesenteric lymph node) show intracellular cytokine staining data indicating that HMBPP stimulation up-regulated numbers of CD3+ IFNγ+Vγ2+ T cells (right) and down-regulated numbers of CD3+IL-22+ T cells (left) in lymphocytes from lungs, spleens and mesenteric lymph nodes (LN). Cells were gated on CD3. Percentage numbers of IL-22+ or IFNγ+Vγ2+ T cells in CD3 T cells are listed above individual histograms, and folds of up-regulation (the ratio of HMBPP-stimulated versus unstimulated) or down-regulation are indicated in parentheses. Note that 1 hour HMBPP stimulation did not increase the number of entire Vγ2Vδ2+ T cells (including both IFNγ+ and IFNγ- Vγ2Vδ2+ T-cell populations) in CD3+; the percentage of Vγ2Vδ2+ T cells in CD3+ remained similar in the presence or absence of HMBPP (HMBPP enabled some IFNγ- Vγ2Vδ2+ T cells to become IFNγ+ Vγ2Vδ2+ T cells). The decreased numbers of IL-22-producing T cells were not due to expansion of Vγ2Vδ2+ T cells after 1-hr HMBPP activation. (B) Comparative analyses of flow-cytometry data indicating that HMBPP stimulation up-regulated percentage numbers of IFNγ+Vγ2+ T cells (top panels) and down-regulated percentage numbers of IL-22+ CD3+ T cells (bottom) in lymphocytes from lungs (n = 6), spleens (n = 8) and mesenteric lymph nodes (n = 5). Data were means ± SEM derived from eight infected rhesus macaques and were gated on CD3. *, P<0.05, ***, P<0.001. (C) Comparative data indicating mean folds of up-regulation of CD3+IFNγ+Vγ2+ T cells (top) and down-regulation of CD3+IL-22+ T cells in lymphocytes from lungs (n = 6), spleens (n = 8) and mesenteric lymph nodes (n = 5). Data were derived from eight infected rhesus macaques and were gated on CD3.