Figure 4.
Figure 4. The interaction between CCL22 and CCR4 is involved in the migration of CD4+CD25+ T cells to tumor sites of B-cell NHL. (A) Dot plots showing the expression of CCR4 and CCR8 on CD4+ T cells from biopsy specimens of B-cell NHL (n = 6). (B) Histograms showing intracellular expression of CCL17 and CCL22 in CD20+ lymphoma B cells from biopsy specimens of B-cell NHL (n = 6). The shaded histogram represents the isotype control staining, and the open histogram represents the CCL17 or CCL22 staining. (C) The bar graph showing CD4+CD25+ T-cell migration in response to supernatant of lymphoma B cells (SP). CD4+CD25+ T cells were labeled with calcein AM, and the fluorescence intensity of migrated cells was measured by fluorescent plate reader. Results are the mean ± SD, n = 6, *P < .01, compared with media alone; #P < .05, compared with supernatant. Patient sample nos. 3, 10, 11, 16, 17, and 20 to 23 were used in these experiments.

The interaction between CCL22 and CCR4 is involved in the migration of CD4+CD25+ T cells to tumor sites of B-cell NHL. (A) Dot plots showing the expression of CCR4 and CCR8 on CD4+ T cells from biopsy specimens of B-cell NHL (n = 6). (B) Histograms showing intracellular expression of CCL17 and CCL22 in CD20+ lymphoma B cells from biopsy specimens of B-cell NHL (n = 6). The shaded histogram represents the isotype control staining, and the open histogram represents the CCL17 or CCL22 staining. (C) The bar graph showing CD4+CD25+ T-cell migration in response to supernatant of lymphoma B cells (SP). CD4+CD25+ T cells were labeled with calcein AM, and the fluorescence intensity of migrated cells was measured by fluorescent plate reader. Results are the mean ± SD, n = 6, *P < .01, compared with media alone; #P < .05, compared with supernatant. Patient sample nos. 3, 10, 11, 16, 17, and 20 to 23 were used in these experiments.

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