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In Vitro Study of Immune Tolerance Induced by CTLA4–Ig in Bone Transplantation: The Effect on Cell Proliferation Stimulated by Lymphocytes and Bone Supernatant

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To clarify the effect of CTLA4–lg on immune rejection of bone grafts, we observed the effect of CTLA4–Ig on lymphocyte proliferation of BALB/C mice stimulated by lymphocytes and bone supernatant of C57BL/6 mice. The splenic lymphocytes and bone supernatant of C57BL/6 mice, as the stimulator cells and stimulator antigens, were cultured in vitro with the splenic lymphocyte of BALB/C mice. At the same time, CTLA4–Ig at a dose of 5,10 or 20 μg/ml and L6 (as control) at 20 μg/ml were added. Six days later, the incorporation of 3H-TdR was determined. Results indicated that CTLA4–Ig at a dose of 5, 10 or 20 μg/ml significantly inhibited the cell proliferation stimulated by lymphocytes and bone supernatant of C57BL/6 mice. The effect was non-cytotoxic. L6 showed no significant inhibition of cell proliferation. CTLA4–Ig can efficiently block the proliferation of alloresponsive T cell stimulated by lymphocytes and bone supernatant of C57BL/6 mice. This study provides a basis for further study of CTLA4-induced immune tolerance of bone grafts.
Title: In Vitro Study of Immune Tolerance Induced by CTLA4–Ig in Bone Transplantation: The Effect on Cell Proliferation Stimulated by Lymphocytes and Bone Supernatant
Description:
To clarify the effect of CTLA4–lg on immune rejection of bone grafts, we observed the effect of CTLA4–Ig on lymphocyte proliferation of BALB/C mice stimulated by lymphocytes and bone supernatant of C57BL/6 mice.
The splenic lymphocytes and bone supernatant of C57BL/6 mice, as the stimulator cells and stimulator antigens, were cultured in vitro with the splenic lymphocyte of BALB/C mice.
At the same time, CTLA4–Ig at a dose of 5,10 or 20 μg/ml and L6 (as control) at 20 μg/ml were added.
Six days later, the incorporation of 3H-TdR was determined.
Results indicated that CTLA4–Ig at a dose of 5, 10 or 20 μg/ml significantly inhibited the cell proliferation stimulated by lymphocytes and bone supernatant of C57BL/6 mice.
The effect was non-cytotoxic.
L6 showed no significant inhibition of cell proliferation.
CTLA4–Ig can efficiently block the proliferation of alloresponsive T cell stimulated by lymphocytes and bone supernatant of C57BL/6 mice.
This study provides a basis for further study of CTLA4-induced immune tolerance of bone grafts.

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