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. Author manuscript; available in PMC: 2008 Nov 25.
Published in final edited form as: J Immunol. 2008 Jul 15;181(2):1153–1160. doi: 10.4049/jimmunol.181.2.1153

Figure 6.

Figure 6

Transduced GILT KO B cells could not induce tolerance to disulfide bond-containing Ag HEL. A, LPS-activated GILT KO or WT C57BL/6 B cells were transduced with HEL-IgG or OVA-IgG as a mock control. Normal C57BL/6 recipients were injected i.p. with 107 transduced B cells. On day 7 postinjection, animals were immunized in a hind footpad and the base of tail with 25 μg of HEL protein emulsified in CFA. Two weeks postimmunization, animals were sacrificed and draining LNs were removed. T cell proliferation to HEL protein was determined by [3H]thymidine incorporation. Values represent mean Δcpm ± SE for four animals. The background [3H]thymidine incorporation was in the range of 13,000–20,000. Data are representative of four independent experiments. *, p < 0.05. B, Animals were treated as described in Fig. 6A. Two weeks postimmunization, sera were assayed by the endpoint ELISA method. The Ab titer was determined by the highest dilution of samples, with an OD450 greater than the negative control (undiluted mouse serum). The result is shown as the mean ± SE of Ab titers. Data are representative of four independent experiments.