Fig. 4.
Fig. 4. Influence of rCD44v4-v7 on antihost reactivity after reconstitution of allogeneic SCID mice. Allogeneic SCID mice were irradiated with 300 R and were reconstituted with 5 × 106 BMC from NTG and rCD44v4-v7 TG C57BL/6 mice. Mice received, in addition, either a control IgG1 or anti-rCD44v6 (200 μg twice per week). TC, SC, and LNC were harvested after 2 to 6 weeks. Cells from 3 mice per group were pooled and were cultured in the presence of irradiated lymphocytes from BALB/c mice. After 3 days of culture and the addition of 3H-thymidine during the last 16 hours, cells were harvested and incorporation of 3H-thymidine was determined in a β-counter. Background values were subtracted (cpm in the absence of an antigenic stimulus). Mean cpm ± SD of triplicate cultures are shown; significant differences between NTG and TG BMC (P ≤ .01) are indicated by an asterisk. The experiment was repeated one time showing similar results.

Influence of rCD44v4-v7 on antihost reactivity after reconstitution of allogeneic SCID mice. Allogeneic SCID mice were irradiated with 300 R and were reconstituted with 5 × 106 BMC from NTG and rCD44v4-v7 TG C57BL/6 mice. Mice received, in addition, either a control IgG1 or anti-rCD44v6 (200 μg twice per week). TC, SC, and LNC were harvested after 2 to 6 weeks. Cells from 3 mice per group were pooled and were cultured in the presence of irradiated lymphocytes from BALB/c mice. After 3 days of culture and the addition of 3H-thymidine during the last 16 hours, cells were harvested and incorporation of 3H-thymidine was determined in a β-counter. Background values were subtracted (cpm in the absence of an antigenic stimulus). Mean cpm ± SD of triplicate cultures are shown; significant differences between NTG and TG BMC (P ≤ .01) are indicated by an asterisk. The experiment was repeated one time showing similar results.

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