Figure 2
Figure 2. SHP-1–deficient T cells are pathogenic and able to induce colitis. CD4+CD25− CD45RBhi T cells (5 × 105) isolated from +/+ or me/+ mice were transferred into rag1−/− recipients. (A) Representative colon segments of recipient mice 7 to 8 weeks after adoptive T-cell transfer (+/+, me/+, and PBS, H&E, original magnification ×200). The arrow points to a giant cell among inflammatory cells. (B) Pathologic scoring of colon segments from recipient mice 7 to 8 weeks after adoptive T-cell transfer (+/+ vs me/+, P = .5, not significant; +/+ vs PBS, P = .001; me/+ vs PBS, P = .02). (C-D) Numbers of IL-17A/F+ T cells within the CD4+ compartment isolated from the lamina propria (C, +/+ vs me/+, P = .5, not significant) and Peyer patches (D, +/+ vs me/+, P = .7, not significant) of the indicated donor-derived populations 7 to 8 weeks after transfer. Data are representative of 3 independent experiments with multiple mice for each genotype per experiment.

SHP-1–deficient T cells are pathogenic and able to induce colitis. CD4+CD25 CD45RBhi T cells (5 × 105) isolated from +/+ or me/+ mice were transferred into rag1−/− recipients. (A) Representative colon segments of recipient mice 7 to 8 weeks after adoptive T-cell transfer (+/+, me/+, and PBS, H&E, original magnification ×200). The arrow points to a giant cell among inflammatory cells. (B) Pathologic scoring of colon segments from recipient mice 7 to 8 weeks after adoptive T-cell transfer (+/+ vs me/+, P = .5, not significant; +/+ vs PBS, P = .001; me/+ vs PBS, P = .02). (C-D) Numbers of IL-17A/F+ T cells within the CD4+ compartment isolated from the lamina propria (C, +/+ vs me/+, P = .5, not significant) and Peyer patches (D, +/+ vs me/+, P = .7, not significant) of the indicated donor-derived populations 7 to 8 weeks after transfer. Data are representative of 3 independent experiments with multiple mice for each genotype per experiment.

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