New TCR transgenic model for tracking allospecific CD4 T-cell activation and tolerance in vivo

作者：Sandner SE; Salama AD; Houser SL; Palmer E; Turka LA; Sayegh MH^*

来源：American Journal of Transplantation, 2003, 3(10): 1242-1250.

DOI：10.1046/j.1600-6143.2003.00220.x

• alloimmunity
• animal model
• rejection
• T cell costimulation
• TCR transgenic mice
• tolerance

We have developed an adoptive transfer model system to visualize the dynamics of alloantigen-specific CD4(+) T-cell activation in vivo. Using TCR-transgenic (tg) mice reactive to I-A(bm12), we studied the clonal expansion and differentiation of alloreactive T cells by tracking the fate of adoptively transferred TCR-tg CD4(+) T cells in syngeneic mice transplanted with skin grafts expressing I-A(bm12). Following transplantation, alloantigen-specific TCR-tg CD4(+) T-cell expansion was observed initially in the draining lymph nodes followed by the spleen. TCR-tg CD4(+) T cells up-regulated CD69 and CD25. expression, developed an effector/memory surface phenotype and produced IFN-gamma in response to alloantigen ex vivo. Furthermore, we validate the model system as a means for studying the effects of tolerogenic regimens on alloreactive CD4(+) T cells, demonstrating that CTLA4Ig inhibits alloantigen-dependent clonal expansion and effector function of TCR-tg CD4(+) T cells in vivo. We describe the first model for tracking alloreactive CD4(+) T-cell. activation in vivo. It provides a powerful tool for studying CD4(+) T-dell mediated alloimmune responses and mechanisms of tolerance induction in vivo.

• 出版日期2003-10